8 Site initiation Jobs nearby Gandhinagar

As an Architectural Drafting Expert, you will play a crucial role in turning building designs into reality. Your responsibilities will include developing concepts for structures and collaborating with engineers to ensure the functionality of designs align with project goals. Here is what you must have: - Bachelor's degree in Architecture (B.Arch) or Interior Design (D.Arch). Candidates with a B.E./Diploma in Civil can also apply. - Proficiency in design software such as AutoCAD, Adobe Photoshop, SketchUp, 3d Studio VIZ, or similar. - Strong drawing skills and the ability to create presentations using AutoCAD, Photoshop, and PowerPoint. - Capacity for independent conceptualization tailored to meet client requirements. - Client-centric approach with excellent communication skills. - Ability to work effectively in both team and individual settings. - Knowledge of building products, construction details, rules, regulations, and quality standards. - Understanding of materials, construction processes, and the ability to think and create in three dimensions. Your role and responsibilities will include: - Understanding client requirements and creating Presentation/Tender/GFC drawings. - Visiting sites to comprehend client needs accurately. - Experience in wooden houses, hotels, resorts, and free fab structures is preferred. - Master planning, layout, elevation, and presentation. - Ensuring high-quality, innovative, and functional design from project initiation to completion. - Identifying client needs, preparing feasibility reports, and design proposals. - Creating design concepts within project timelines and costs. - Preparing Bill of Quantities, Pert charts, and project schedules. - Site supervision, project management, and coordination with contractors/vendors. - Interaction with clients, attending meetings, and certifying bills submitted by vendors. - Collaboration with design consultants and internal teams to finalize designs. - Educating clients about the company's design and execution capabilities. This job is located in Rajkot, and candidates with 0-2 years of experience are encouraged to apply. As an Architectural Drafting Expert, you will play a crucial role in turning building designs into reality. Your responsibilities will include developing concepts for structures and collaborating with engineers to ensure the functionality of designs align with project goals. Here is what you must have: - Bachelor's degree in Architecture (B.Arch) or Interior Design (D.Arch). Candidates with a B.E./Diploma in Civil can also apply. - Proficiency in design software such as AutoCAD, Adobe Photoshop, SketchUp, 3d Studio VIZ, or similar. - Strong drawing skills and the ability to create presentations using AutoCAD, Photoshop, and PowerPoint. - Capacity for independent conceptualization tailored to meet client requirements. - Client-centric approach with excellent communication skills. - Ability to work effectively in both team and individual settings. - Knowledge of building products, construction details, rules, regulations, and quality standards. - Understanding of materials, construction processes, and the ability to think and create in three dimensions. Your role and responsibilities will include: - Understanding client requirements and creating Presentation/Tender/GFC drawings. - Visiting sites to comprehend client needs accurately. - Experience in wooden houses, hotels, resorts, and free fab structures is preferred. - Master planning, layout, elevation, and presentation. - Ensuring high-quality, innovative, and functional design from project initiation to completion. - Identifying client needs, preparing feasibility reports, and design proposals. - Creating design concepts within project timelines and costs. - Preparing Bill of Quantities, Pert charts, and project schedules. - Site supervision, project management, and coordination with contractors/vendors. - Interaction with clients, attending meetings, and certifying bills submitted by vendors. - Collaboration with design consultants and internal teams to finalize designs. - Educating clients about the company's design and execution capabilities. This job is located in Rajkot, and candidates with 0-2 years of experience are encouraged to apply.

Role Overview: You will be joining Siemens Energy as a Commercial Project Manager (Finance), where you will be responsible for overseeing technical, administrative, and commercial activities at the site. Your role will involve leading and managing projects, ensuring compliance with regulations, managing project finances, and handling risk, contract, and claims management. Key Responsibilities: - Lead and manage projects throughout the entire project life cycle, including sales and project initiation phases. - Review and evaluate contract conditions, conduct commercial project status meetings, and ensure adherence to regulations. - Verify cost and pricing calculations, prepare commercial documentation, and manage asset management and invoicing per project progress. - Ensure compliance with Siemens FRG and local GAAP requirements, oversee financial guarantees, bonds, and project securities. - Participate in contract/claim/change order negotiations, identify and respond to commercial risks, and communicate relevant contractual obligations. - Lead project members to adhere to Business Conduct Guidelines and ensure compliance with tax regulations and export control regulations. Qualifications Required: - Qualified CA / ICWA / CMA / MBA - finance or related field with Six to Eight Years of experience. - Proven Six to Eight Years of experience in commercial project management. - Strong understanding of financial principles, project management methodologies, negotiation, and contract management skills. - Familiarity with relevant regulations and compliance standards. - Leadership, team management, problem-solving, analytical, communication, and interpersonal skills. - Proficiency in SAP and Microsoft Office Suite. Company Details (if any): Siemens Energy is dedicated to equality and diversity, making employment decisions based on qualifications, merit, and business needs. As part of a global team of over 379,000 employees in over 200 countries, you will have the opportunity to work with diverse teams shaping the future of the energy industry and making a worldwide impact. This role is based in Thane, with the potential for travel across India and internationally for various project activities.,

Job Description: As a SAP PM Consultant at AMNS GROUP in Surat, you will be responsible for SAP project management, plant maintenance, business process analysis, and project implementation on a day-to-day basis. Your role will be full-time on-site focusing on ensuring efficient project delivery and maintenance operations. Key Responsibilities: - Manage SAP projects from initiation to completion, ensuring timely delivery and meeting project objectives - Conduct business process analysis to identify areas for improvement and optimization - Implement SAP solutions for plant maintenance, ensuring smooth operations and minimal downtime - Utilize analytical skills to troubleshoot issues and provide effective solutions - Collaborate with cross-functional teams to ensure seamless project implementation - Communicate effectively with stakeholders to gather requirements and provide project updates Qualifications Required: - Proficiency in SAP Project Management and Project Implementation - Strong analytical skills and in-depth business process knowledge - Hands-on experience in Plant Maintenance within SAP environment - Ability to solve complex problems efficiently - Excellent communication and interpersonal abilities to interact with diverse teams - Possession of relevant SAP certifications would be advantageous - Bachelor's degree in Information Technology, Computer Science, or a related field (Note: No additional details about the company were provided in the job description.),

As an Officer/Sr. Officer in the Consumer Research Department at our company based in Ahmedabad, your role involves: - Identifying and qualifying potential investigators for research studies. - Collecting necessary documents to assess site/investigator feasibility and obtain approval from authorities. - Training the site study team, maintaining essential documents, and overseeing startup activities and site initiation. - Conducting monitoring visits to ensure compliance with study management, protocol, and other requirements at all assigned sites. - Performing source document verification as per the monitoring plan to maintain accurate and up-to-date trial records. - Coordinating with labs and other trial-related services as needed and ensuring IP accountability and availability. - Managing all clinical trial-related supplies, including tracking, shipping, and vendor management. - Handling site closeout and follow-up activities to maintain proper documentation. - Assisting with site audits and liaising with Quality Assurance personnel to ensure compliance with ICH GCP and regulatory guidelines. Basic qualifications required for this role are B. Pharm/M. Pharm/M. Sc with 2-4 years of relevant experience. If you are interested in this opportunity, please send your resume to apurohit@cliantha.com.,

As a Civil Engineer at The Arete Group, you will be responsible for project planning, scheduling, and resource management with expertise in Microsoft Project (MSP). Your role will involve overseeing complex construction projects from design to completion, ensuring timely delivery, cost control, and adherence to quality and safety standards. Your proficiency in MSP will be crucial for optimizing workflows, tracking milestones, and managing project timelines efficiently. Your strong communication skills, team coordination abilities, and problem-solving mindset will contribute to delivering efficient and cost-effective engineering solutions. **Key Responsibilities:** - Create and manage detailed project schedules using Microsoft Project, including critical path and milestone tracking. (At least completed 1-2 projects in MS project from start to delivery.) - Project control and reporting Project planning in MS Project software, monitoring and control, critical path analysis, resource management, cost management, baseline management, issue management, look ahead schedules, schedule crashing if it is getting delayed. - Tracking project progress against planned timelines and budgets, identifying any deviation and implementing corrective actions. - Prepare MIS and circulate MIS to all the relevant internal stakeholders and escalate to project head as needed, providing regular updates to various stakeholders about strategy, adjustments and progress. - Assist in organizing project meetings, including scheduling, preparing agendas, and recording meeting minutes. - Maintain accurate records of project documentation, including RFI logs, submittals, and change orders. - Maintain digital records and documentation following company protocols and regulatory requirements. - Coordinate between the construction site and the design office for design and drawing issues. **Qualifications Required:** - Hands-on experience with Microsoft Project for effective planning, scheduling, tracking, and controlling projects across all phases and scales. - Successfully delivered complete project cycles from initiation to closure for 3 to 4 projects, utilizing Microsoft Project for comprehensive planning, scheduling, and monitoring. - Handled projects with a minimum valuation of 100 crore, ensuring effective planning, execution, and control. - Strong knowledge of site execution processes and practices. **Behavioural Skills Required:** - Communication: Clear, concise verbal and written communication with all stakeholders. - Organizational Skills: Strong time management to juggle multiple tasks, documents, and schedules. - Problem Solving: Quick thinking to resolve on-site issues without delaying the schedule. - Teamwork and Collaboration: Works well with field crews, engineers, architects, and clients. - Adaptability: Comfortable working in a dynamic, fast-changing construction environment. - Attention to Detail: Accuracy in managing documents, plans, and schedules. - Leadership (without authority): Influences subcontractors and site workers to stay on task and meet deadlines. - Emotional Intelligence: Stays calm under pressure and maintains a professional demeanor. - Accountability: Owns tasks and follows through without constant supervision. - Conflict Resolution: Mediates disputes between stakeholders effectively.,

Role Overview: You will be joining as a Project Manager in our office located in Ahmedabad. Your primary responsibility will be to manage a design project from its initiation to completion. This includes defining timelines, budgets, maintaining client and consultant relationships. As a Project Manager, you will have the opportunity to work on a diverse range of projects across India. Key Responsibilities: - Prepare project briefs, schedules, and cost estimates at different stages of the project. - Finalize and onboard various consultants, experts, and advisors for the project. - Represent the company at various forums, client groups, and stakeholder meetings. - Organize meetings as necessary and prepare notes and minutes of meetings. - Coordinate with the design team, consultants, and contractors to enhance the project's design. - Lead and manage the schedule and budget throughout the project life cycle. - Draft letters, emails, MoMs, project notes, etc., in grammatically correct English. - Conduct periodic site visits to ensure adherence to design and resolve site issues. - Support the Business Development team in contracts and proposals. Qualifications Required: - Mandatory: A bachelor's or master's degree in civil engineering or construction management. - Preferred: Master's degree in project management. Additional Details: (if present in the JD) The company is focused on Project & Construction Management industry. You are expected to possess excellent communication skills, good interpersonal skills, analytical skills, planning and organizing skills, leadership skills, and proficiency in MS Office and MS Projects. Additionally, you should have an understanding of design concepts, drawings, construction codes, and standards. Your ability to think rationally and resolve issues with a solution-oriented approach will be crucial in this role.,

The Sales Executive role at BrainADZ Exhibits is a full-time on-site position based in Dwarka, New Delhi. Your primary responsibilities will include: - Identifying and acquiring new clients - Nurturing relationships with existing clients - Understanding client needs to deliver customized exhibition stall design and fabrication solutions Your daily tasks will involve: - Reaching out to potential clients through calls and meetings - Creating proposals - Engaging in negotiations - Overseeing the entire sales process from initiation to closure Additionally, you will collaborate with the 3-D design and production teams to ensure the timely delivery of stalls and to guarantee client satisfaction. To excel in this role, you should ideally have experience in Stall Design Sales or related experience in the Expo Industry. Strong communication, presentation, and negotiation skills are essential for effectively engaging with clients. The ability to work both independently and as part of a team is crucial for success in this position. A Bachelor's degree in Business, Marketing, or a related field is preferred, and any prior experience in event management or the exhibition industry would be advantageous. BrainADZ Exhibits is a reputable industry leader renowned for its expertise in designing and constructing high-quality stalls for exhibitions and events on a global scale. With multiple in-house production and storage facilities in key cities across India and Dubai, the company offers tailored solutions to clients in various regions such as India, USA, Canada, Middle East, Europe, Italy, and China. If you are passionate about sales, have a flair for design, and enjoy working in a dynamic environment, we invite you to apply for the Sales Executive position at BrainADZ Exhibits. Kindly send your CV to sumit@brainadz.com to be considered for this exciting opportunity. For more information about the company, please visit the website at www.brainADZexhibits.com.,

As an Inside Sales Executive based in Vadodara, Gujarat, India, your role is crucial in contributing to the business's growth by identifying new customers, qualifying leads, and finalizing sales. Your primary responsibilities will include making outbound calls, sending emails, and delivering service presentations to potential clients. Building and maintaining relationships with leads, guiding them through the sales process, and achieving sales targets are essential aspects of this role. It is important to note that working US shift hours is a requirement to engage with clients from the US effectively. Your key responsibilities will involve: - Making 80-120 outbound calls daily to potential prospects in the US - Understanding their business goals to qualify leads - Conducting 1-2 virtual or in-person sales presentations each day - Ensuring regular follow-ups with leads to sustain engagement and progress in the sales process - Managing the sales process from initiation to completion while ensuring thorough documentation - Meeting monthly and quarterly sales objectives - Tracking sales activities in CRM - Collaborating with the sales and operations teams to facilitate the onboarding of new clients To qualify for this role, you should possess: - A Bachelor's degree or equivalent, with a Master's degree considered advantageous - Previous experience of 0-2 years in sales, business development, or a related field is preferred, although freshers are also encouraged to apply - Strong communication skills - Proficiency in using CRM systems and productivity tools like MS Office - An interest in sales with a commitment to learning and achieving targets - Multitasking abilities - Organizational skills - Teamwork capabilities - Willingness to work US shift hours Joining this role offers a competitive salary with performance-based rewards, growth prospects in a dynamic company, as well as training and support essential for your success. Please note that this position entails working in the office for five days a week during US shift hours. The job type is full-time, on-site, and the salary ranges from 10k-15k, depending on the interview. The shift timings are during US Shift (evening/night hours), with a fixed salary range of 15-20k along with incentives (no upper limit on incentives). If you are ready to take on this exciting opportunity to contribute to the company's growth and achieve sales targets while working in a dynamic environment, we encourage you to apply and be a part of our team in Vadodara.,

Role Overview: As a Site Engineer at Reliance Industries, your main responsibility will be to oversee day-to-day construction activities to ensure that projects are completed on time, within budget, and to specified quality and safety standards. You will supervise site work, coordinate with contractors, manage schedules and resources, enforce safety protocols, and prepare progress reports and documentation. Your role will require a Civil Engineering degree and skills in project scheduling, quality assurance, and problem-solving. Key Responsibilities: - Supervise and manage site activities: Oversee all day-to-day construction and fit-out activities from initiation to completion. - Ensure quality and safety: Supervise the execution of work, ensuring adherence to design, quality, and safety standards, and enforcing safety protocols. - Coordinate with stakeholders: Liaise with contractors, subcontractors, vendors, architects, and other engineers to ensure timely delivery of materials and services. - Manage schedules and budgets: Ensure project schedules and timelines are managed effectively to complete projects within defined budgets. - Monitor and report progress: Conduct site progress reporting, maintain site records, and update project schedules. - Handle technical issues: Identify and resolve site issues or discrepancies promptly to prevent project delays. - Ensure compliance: Make sure that all construction activities comply with building codes, statutory requirements, and company policies. - Support administrative tasks: Assist in vendor bill verification, measurement certification, and documentation for billing. Qualifications Required: - Education: A Bachelor's degree in Civil Engineering or a related field is typically required. - Experience: Relevant experience in construction is often necessary, though some roles may be entry-level. - Technical Skills: Strong knowledge of civil construction methods and materials, familiarity with tools like Civil 3D and STAAD.Pro can be beneficial, and technical knowledge specific to the project type may be required. - Soft Skills: Project management, coordination, problem-solving, communication, interpersonal skills, planning, organizational skills, attention to detail, and record-keeping. Additional Company Details: No additional details about the company were provided in the job description.,

You will be responsible for visiting customer sites to verify and assess site conditions before design and execution. You will ensure accurate site measurements, validate service points, and identify feasibility or structural issues before project kickoff. - Visit customer sites to measure, assess, and validate the space for design and execution feasibility. - Verify civil and modular work requirements, including electrical, plumbing, and structural readiness. - Identify and document site challenges, deviations, or risks before project initiation. - Capture accurate measurements, photographs, and validation reports for design and estimation teams. - Coordinate with design, sales, and execution teams for project handover and approvals. - Ensure all validations meet quality, safety, and accuracy standards. **Qualifications & Experience** - Education: Diploma or Bachelor's degree in Civil Engineering, Interior Design, or Architecture. - Experience: 13 years of on-site experience in modular interiors and civil work validation. - Strong technical knowledge of interior layouts, carpentry, and site services. - Excellent attention to detail and documentation skills. - Good communication and coordination abilities with cross-functional teams. - Proficiency in measurement tools and basic MS Office reporting. You will have the opportunity to be a part of India's leading PropTech brand shaping the home interiors industry. Additionally, you will get to work on diverse residential and renovation projects with growth opportunities in design validation and project operations.,

You will be working as a Clinical Trial Manager (CTM) at Bristol Myers Squibb, where you will be responsible for end-to-end study operational oversight and delivery at the country level. Your role will involve ensuring adherence to timelines, budget, and quality standards while acting as the primary point of contact for both internal and external stakeholders. Your main duties and responsibilities will include: - Acting as the main point of contact for a country with global study team members and coordinating with local country cross-functional teams. - Implementing the local country and site feasibility process, including proposing and validating country study targets endorsed by country leadership. - Planning, developing, and executing timelines and activities for start-up in collaboration with the local study team, Global Trial Acceleration Centre (GTAC), and other relevant stakeholders. - Implementing country and site-level patient recruitment strategy and risk mitigation. - Leading problem-solving and resolution efforts, including management of risk, contingencies, issue resolution, and escalation to appropriate stakeholders. - Ensuring data entered in the Clinical Trial Management System (CTMS) is current and complete, and access to eDC and vendor systems is available for country and clinical trial site personnel. Qualifications required for this role include a Bachelor's or Master's degree in life sciences or equivalent, along with a minimum of 4 years" industry-related experience as a Clinical Trial Manager. You should have a thorough understanding of GCP, ICH Guidelines, and the country regulatory environment, as well as strong communication skills and the ability to manage multiple competing priorities effectively. The software that you must be able to use independently and without assistance includes Microsoft Suite, Clinical Trial Management Systems (CTMS), Electronic Data Capture Systems (eDC), and Electronic Trial Master File (eTMF). Occasional local travel may be required for this role. If you find a role that interests you but doesn't align perfectly with your resume, Bristol Myers Squibb encourages you to apply anyway. The company values individual talents and unique perspectives, promoting global participation in clinical trials while upholding shared values of passion, innovation, urgency, accountability, inclusion, and integrity.,

As a Clinical Trial Associate (CTA) at our company, you will play a crucial role in supporting the planning, execution, and management of clinical trials while ensuring compliance with regulatory guidelines and company protocols. Your strong organizational skills, excellent communication abilities, and effective collaboration with cross-functional teams will be key to success in this role. **Key Responsibilities:** - Assist in coordinating and managing clinical trials from initiation to completion. - Maintain and update trial documentation, such as investigator brochures, protocols, and informed consent forms. - Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies. - Support the preparation and submission of regulatory documents to relevant authorities and ethics committees. - Track and manage trial-related materials, including investigational products and supplies. - Assist with site selection, activation, and ongoing monitoring activities. - Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations. - Organize and participate in clinical team meetings, taking minutes and following up on action items. - Assist in processing and tracking study invoices, contracts, and budgets. - Maintain trial master files (TMF) and ensure proper documentation for audits and inspections. **Qualifications & Requirements:** - Bachelor's degree in life sciences, healthcare, or a related field. - 1-3 years of experience in clinical research, preferably in a CTA or similar role. - Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards. - Strong attention to detail and organizational skills. - Excellent communication and interpersonal skills. - Proficiency in Microsoft Office (Word, Excel, PowerPoint) and G Suite. - Ability to multitask, prioritize, and work independently in a fast-paced environment. **Preferred Qualifications:** - Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting. - Certification in clinical research (e.g., ACRP, SOCRA) is advantageous. Please submit your CV and any relevant portfolio materials to Divjyot.kaur@sova.health. This job offers a competitive salary and benefits package, opportunities for professional growth and development, and a collaborative and inclusive work environment. As a Clinical Trial Associate (CTA) at our company, you will play a crucial role in supporting the planning, execution, and management of clinical trials while ensuring compliance with regulatory guidelines and company protocols. Your strong organizational skills, excellent communication abilities, and effective collaboration with cross-functional teams will be key to success in this role. **Key Responsibilities:** - Assist in coordinating and managing clinical trials from initiation to completion. - Maintain and update trial documentation, such as investigator brochures, protocols, and informed consent forms. - Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies. - Support the preparation and submission of regulatory documents to relevant authorities and ethics committees. - Track and manage trial-related materials, including investigational products and supplies. - Assist with site selection, activation, and ongoing monitoring activities. - Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations. - Organize and participate in clinical team meetings, taking minutes and following up on action items. - Assist in processing and tracking study invoices, contracts, and budgets. - Maintain trial master files (TMF) and ensure proper documentation for audits and inspections. **Qualifications & Requirements:** - Bachelor's degree in life sciences, healthcare, or a related field. - 1-3 years of experience in clinical research, preferably in a CTA or similar role. - Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards. - Strong attention to detail and organizational skills. - Excellent communication and interpersonal skills. - Proficiency in Microsoft Office (Word, Excel, PowerPoint) and G Suite. - Ability to multitask, prioritize, and work independently in a fast-paced environment. **Preferred Qualifications:** - Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting. - Certification in clinical research (e.g., ACRP, SOCRA) is advantageous. Please submit your CV and any relevant portfolio materials to Divjyot.kaur@sova.health. This job offers a competitive salary and benefits package, opportunities for professional growth and development, and a collaborative and inclusive work environment.

As a Clinical Research Coordinator, your role involves organizing and maintaining trial documentation, coordinating study visits, and managing regulatory binders. You will be responsible for assisting in enrolling participants and ensuring compliance with trial protocols. Your duties will also include collecting, entering, and maintaining trial data while ensuring accuracy. Additionally, you will assist with ethics submissions, site initiation, and adherence to Good Clinical Practice (GCP) guidelines. Key Responsibilities: - Organize and maintain trial documentation - Coordinate study visits and manage regulatory binders - Assist in enrolling participants and ensure compliance with trial protocols - Collect, enter, and maintain trial data with accuracy - Assist with ethics submissions, site initiation, and adherence to GCP guidelines - Manage trial supplies, schedule meetings, and ensure smooth operations Qualifications Required: - Previous experience in clinical research coordination - Knowledge of Good Clinical Practice guidelines - Strong organizational and communication skills - Attention to detail and accuracy in data management - Ability to work well in a team and independently - Bachelor's degree in a relevant field preferred Please note that this is a full-time position with day shift, morning shift, and weekend availability required. The work location is in person. As a Clinical Research Coordinator, your role involves organizing and maintaining trial documentation, coordinating study visits, and managing regulatory binders. You will be responsible for assisting in enrolling participants and ensuring compliance with trial protocols. Your duties will also include collecting, entering, and maintaining trial data while ensuring accuracy. Additionally, you will assist with ethics submissions, site initiation, and adherence to Good Clinical Practice (GCP) guidelines. Key Responsibilities: - Organize and maintain trial documentation - Coordinate study visits and manage regulatory binders - Assist in enrolling participants and ensure compliance with trial protocols - Collect, enter, and maintain trial data with accuracy - Assist with ethics submissions, site initiation, and adherence to GCP guidelines - Manage trial supplies, schedule meetings, and ensure smooth operations Qualifications Required: - Previous experience in clinical research coordination - Knowledge of Good Clinical Practice guidelines - Strong organizational and communication skills - Attention to detail and accuracy in data management - Ability to work well in a team and independently - Bachelor's degree in a relevant field preferred Please note that this is a full-time position with day shift, morning shift, and weekend availability required. The work location is in person.

As the Administrative and Operations support for the Managing Director (MD) of Zoetis India Limited (ZIL) in Mumbai, your role involves providing efficient admin support to the General Manager (GM) by managing their calendar, scheduling meetings, appointments, and travel arrangements. Additionally, you will be responsible for organizing detailed domestic and international travel itineraries and logistics, preparing monthly expense reports in Concur, drafting meeting agendas, minutes, and action items, and coordinating logistics for team visits to India. Building and maintaining strong relationships with internal teams, stakeholders, and external partners is essential for smooth operations. Your key responsibilities include: - Managing the GM's calendar efficiently, including scheduling meetings, appointments, and travel arrangements. - Organizing detailed domestic and international travel itineraries and logistics. - Preparing and submitting monthly expense reports in Concur. - Drafting, circulating, and following up on meeting agendas, minutes, and action items. - Coordinating logistics for regional and global team visits to India. - Maintaining strong working relationships with internal teams, stakeholders, and external partners. - Providing administrative support for Board Meetings and ensuring smooth execution. - Reviewing and verifying all legal documents prior to the GM's signature. - Managing membership renewals for industry associations. - Coordinating content for bi-monthly and quarterly business reviews. In terms of commercial support, you will be involved in event and meeting management, procurement support to teams, distributor market compliance, and contract initiation & vendor creation for Strategy & Learning & Development Projects. Support to Zoetis India Limited (ZIL) includes: - Travel & Expense Management: Acting as the single point of contact for all ZIL employee travel-related queries and managing @Work access for approving new card requests. - Administrative & Asset Management: Managing office service functions including telecommunication, visiting cards, stationery, and courier services. - Internal Communication & Policy Management: Leading and managing internal communication initiatives and employee engagement through the Yammer platform. - Site Administration: Working closely with the facilities manager to ensure all processes and procedures for the office site are in place. This role requires meticulous attention to detail, strong organizational skills, and the ability to effectively manage multiple tasks simultaneously. Your contributions will play a vital role in ensuring the smooth functioning of operations and supporting the growth of Zoetis India Limited (ZIL). As the Administrative and Operations support for the Managing Director (MD) of Zoetis India Limited (ZIL) in Mumbai, your role involves providing efficient admin support to the General Manager (GM) by managing their calendar, scheduling meetings, appointments, and travel arrangements. Additionally, you will be responsible for organizing detailed domestic and international travel itineraries and logistics, preparing monthly expense reports in Concur, drafting meeting agendas, minutes, and action items, and coordinating logistics for team visits to India. Building and maintaining strong relationships with internal teams, stakeholders, and external partners is essential for smooth operations. Your key responsibilities include: - Managing the GM's calendar efficiently, including scheduling meetings, appointments, and travel arrangements. - Organizing detailed domestic and international travel itineraries and logistics. - Preparing and submitting monthly expense reports in Concur. - Drafting, circulating, and following up on meeting agendas, minutes, and action items. - Coordinating logistics for regional and global team visits to India. - Maintaining strong working relationships with internal teams, stakeholders, and external partners. - Providing administrative support for Board Meetings and ensuring smooth execution. - Reviewing and verifying all legal documents prior to the GM's signature. - Managing membership renewals for industry associations. - Coordinating content for bi-monthly and quarterly business reviews. In terms of commercial support, you will be involved in event and meeting management, procurement support to teams, distributor market compliance, and contract initiation & vendor creation for Strategy & Learning & Development Projects. Support to Zoetis India Limited (ZIL) includes: - Travel & Expense Management: Acting as the single point of contact for all ZIL employee travel-related queries and managing @Work access for approving new card requests. - Administrative & Asset Management: Managing office service functions including telecommunication, visiting cards, stationery, and courier services. - Internal Communication & Policy Management: Leading and managing internal communication initiatives

As a Clinical Trial Associate (CTA) at our company, your role will involve supporting the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. Your strong organizational skills, excellent communication, and ability to collaborate effectively with cross-functional teams will be essential for success in this role. **Key Responsibilities:** - Assist in the coordination and management of clinical trials from initiation to completion. - Maintain and update trial documentation, including investigator brochures, protocols, and informed consent forms. - Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies. - Support the preparation and submission of regulatory documents to relevant authorities and ethics committees. - Track and manage trial-related materials, including investigational products and supplies. - Assist with site selection, activation, and ongoing monitoring activities. - Communicate with investigators, site staff, vendors, and internal stakeholders to facilitate smooth trial operations. - Organize and participate in clinical team meetings, taking minutes and following up on action items. - Assist in processing and tracking study invoices, contracts, and budgets. - Maintain trial master files (TMF) and ensure proper documentation for audits and inspections. **Qualifications & Requirements:** - Bachelor's degree in life sciences, healthcare, or a related field. - 1-3 years of experience in clinical research, preferably in a CTA or similar role. - Knowledge of ICH-GCP guidelines, FDA regulations, and other relevant clinical research standards. - Strong attention to detail and organizational skills. - Excellent communication and interpersonal skills. - Proficiency in Microsoft Office (Word, Excel, PowerPoint) and G Suite. - Ability to multitask, prioritize, and work independently in a fast-paced environment. **Preferred Qualifications:** - Experience working in a pharmaceutical, biotech, or contract research organization (CRO) setting. - Certification in clinical research (e.g., ACRP, SOCRA) is advantageous. In addition to the exciting responsibilities and qualifications required for this role, we offer a competitive salary and benefits package, opportunities for professional growth and development, and a collaborative and inclusive work environment. If you are interested in joining our team, please submit your CV and any relevant portfolio materials to Divjyot.kaur@sova.health.,

As a Construction Site Engineer at our PMC Company in Visakhapatnam (Vizag), Andhra Pradesh, you will play a crucial role in overseeing civil and infrastructure projects. With 3-5 years of experience, including PMC experience, you will be responsible for managing construction sites, ensuring compliance with safety standards, and delivering projects within deadlines and budgets. Preference will be given to local candidates familiar with Vizag's regulatory environment, suppliers, and workforce. **Key Responsibilities:** - Plan, execute, and monitor construction projects from initiation to completion. - Supervise on-site activities to ensure work is carried out as per design, quality, and safety standards. - Manage Main contractor and design Coordination. - Coordinate with architects, engineers, subcontractors, and vendors. - Manage project schedules, budgets, resources, and reporting. - Ensure compliance with local building codes, safety regulations, and environmental guidelines. - Conduct regular progress meetings with clients and stakeholders. - Resolve technical issues and delays promptly. - Maintain project documentation, contracts, and reports. - QA/QC Works and reporting. **Qualifications & Skills:** - Bachelors degree in Civil Engineering, Construction Management, or a related field. - Minimum 5 years of experience in construction project management. - Strong knowledge of construction methods, safety standards, and local building regulations. - Excellent leadership, problem-solving, and communication skills. - Proficiency in MS Project/Primavera/AutoCAD preferred. - Ability to manage multiple contractors and local workforce. - Preference for candidates based in Vizag or nearby areas. If you are passionate about managing construction projects, ensuring quality and safety standards, and delivering projects successfully within deadlines and budgets, we encourage you to apply. Join us in our mission to work on prestigious infrastructure and real estate projects in Vizag and Hyderabad. Competitive salary (based on experience) - Rs 4 LPA, along with performance-based incentives, awaits the right candidate. Send your CV via email to mskcepl@gmail.com.,

As a fresher in the field of research and regulatory affairs, you will be responsible for completing appropriate role-specific training to perform job duties. Under supervision, you will assist in various administrative tasks to support team members in project execution. This may include running system reports, maintaining meeting minutes, preparing and distributing status reports, creating and managing study documents, and more. - Assist in various administrative tasks to support team members in project execution - Run system reports, maintain meeting minutes, prepare and distribute status reports - Create and manage study documents Your role will also involve updating and maintaining systems within project timelines and per project plans. Ensuring the accuracy and completeness of source documents, CRFs, Investigator Site File, and other study-related documents according to ICH-GCP guidelines will be crucial. Additionally, you will be responsible for completing the eCRF and maintaining Investigational Product integrity based on specific temperature requirements. - Update and maintain systems within project timelines and per project plans - Ensure accuracy and completeness of study-related documents according to ICH-GCP guidelines - Complete eCRF and maintain Investigational Product integrity Furthermore, you will play a vital role in preparing for site qualification visits, initiation visits, monitoring visits, and site close-out visits. Organizing ethics committee meetings, completing review forms, and submitting all study-related documents to EC will also be part of your duties. You may need to coordinate with local and central labs, assist in Safety Reporting within required timelines, contribute to patient selection and recruitment processes, and support the Informed Consent Process. - Prepare for various site visits and meetings - Coordinate with local and central labs - Support Safety Reporting and patient recruitment processes To excel in this position, you should possess basic knowledge of applicable research and regulatory requirements such as ICH GCP and relevant local laws, regulations, and guidelines. Proficiency in MS Applications like Microsoft Word, Excel, and PowerPoint is essential. Strong written and verbal communication skills in English, effective time management abilities, and a results-oriented approach to work delivery will be critical for success. - Possess basic knowledge of research and regulatory requirements - Proficiency in MS Applications - Strong communication skills and time management abilities Moreover, you should be capable of establishing and maintaining effective working relationships with coworkers, managers, and clients. Strong listening and phone skills, as well as good data entry abilities, are also required to fulfill the responsibilities of this role. - Establish and maintain effective working relationships - Possess strong listening and phone skills - Have good data entry abilities **Qualifications Required:** - Educational backgrounds in B.Tech, M.Tech (Biotechnology), MSc (Biotechnology, Microbiology, Biochemistry), B.Pharm, M.Pharm, Pharm D, MSc, and BSc (Life Science: Bioinformatics, Biomedical Engineering, etc.) from the years 2016 to 2019 are encouraged to apply for this position.,

As a Clinical Trials Assistant, your role will involve assisting in the preparation and coordination of clinical trial protocols and associated documents. You will support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out. Your responsibilities will include ensuring that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements. Additionally, you will conduct site visits to assess the progress of clinical trials, monitor data accuracy, and ensure patient safety. Key Responsibilities: - Assist in the review and management of clinical trial documentation, including case report forms (CRFs), informed consent forms, and regulatory submissions. - Maintain study files and data to ensure compliance with applicable regulatory agencies. - Support the clinical team in preparing reports, including monitoring reports and other regulatory documents. - Attend and participate in internal meetings, as well as relevant training sessions, to develop knowledge and skills in clinical research. Qualifications Required: - Prior experience or education in clinical research or a related field. - Knowledge of Good Clinical Practice (GCP) guidelines. - Strong attention to detail and organizational skills. In addition to the above, the company offers benefits including health insurance, paid sick time, and Provident Fund. The work location for this position is in person. Please note that this is a full-time position suitable for freshers.,

As a Project Control & Planning member, you play a crucial role in supporting the project management team to ensure the successful execution of solar projects. Your main responsibilities will involve: - Assisting project managers in planning, scheduling, and coordinating solar energy projects from initiation to completion. - Collaborating with internal teams like engineering, procurement, and installation to guarantee smooth project execution. - Monitoring project progress, identifying risks, proposing solutions, preparing project documentation, and managing project budgets. - Coordinating with subcontractors and vendors to ensure project milestones are achieved and deadlines are met. Moreover, you will assist in conducting site visits and inspections, communicate effectively with clients to provide updates and address concerns, and contribute to continuous improvement initiatives by implementing best practices in project management processes. It is essential to stay updated on industry trends, technologies, and regulations related to solar energy and project management. Qualifications required for this role include: - Bachelor's degree in engineering, business administration, project management, or related field. - Prior experience in project management, preferably in the renewable energy or construction industry. - Strong organizational skills, excellent communication and interpersonal skills. - Proficiency in project management software and knowledge of solar energy systems. - Certification in project management (e.g., PMP) is desirable but not mandatory.,

Role Overview: PunchWork Interior is looking for a skilled Project Manager to join their team and oversee all phases of interior fit-out projects, ensuring high-quality design solutions are delivered seamlessly. As a Project Manager, you will collaborate with clients, develop project plans and budgets, coordinate with stakeholders, and ensure compliance with safety regulations and industry standards. Your role will involve managing project risks, conducting site visits, and communicating effectively with all stakeholders. Key Responsibilities: - Manage and oversee all phases of interior fit-out projects from initiation to completion. - Collaborate with clients to understand their needs and align project specifications with their vision. - Develop detailed project plans, timelines, and budgets, ensuring adherence to schedules and financial limitations. - Coordinate with subcontractors, suppliers, and internal teams to maintain project workflow and timelines. - Conduct regular site visits to monitor progress, quality of work, and address any issues promptly. - Ensure compliance with safety regulations and industry standards throughout the project lifecycle. - Communicate project updates to all stakeholders, maintaining transparency and managing expectations effectively. - Identify and mitigate project risks, implementing contingency plans as needed. Qualifications: - Bachelor's degree in Construction Management, Civil Engineering, Architecture, or a related field. - Minimum of 5 years of experience in project management, specifically in interior fit-outs or related construction projects. - Experience in Project Management, including planning and execution. - Skills in Expediting and Logistics Management. - Inspection skills to ensure quality standards are met. - Outstanding organizational and multitasking abilities. - Excellent communication and leadership skills. - Ability to work on-site and manage multiple projects simultaneously. - Previous experience in interior design or related industry is beneficial. - Strong understanding of construction processes, materials, and legal regulations. - Ability to read and interpret drawings, plans, and specifications. - PMP or equivalent project management certification is preferred. Additional Company Details: PunchWork Interior provides end-to-end modular interior design solutions, connecting manufacturers directly to consumers. The company prides itself on delivering innovative and cost-effective solutions tailored to meet individual needs in a dynamic and customer-focused environment. Joining the team at PunchWork Interior offers the opportunity to be part of a seamless approach to high-quality interior design projects without any hassle. Note: This is an urgent vacancy.,