1,730 Trials Jobs in Tiruppur

Role Overview: You will be responsible for planning, coordinating, and executing clinical programs to promote the concept of ECMO, Counter Pulsation therapy, and Advance Hemodynamics monitoring (AdMon). Additionally, conducting in-service education programs for new and existing users to enhance confidence and maximize the usage of ECMO, IABP, and AdMon will be a key part of your role. Key Responsibilities: - Provide information to Physicians & Allied Health Professionals by discussing/detailing the latest clinical trials. - Conduct in-service education programs for new and existing users to improve confidence and maximize usage of ECMO, IABP, and AdMon. - Offer product support to users through in-person interactions, as well as written or verbal means. - Extend patient support at short notice. - Provide product training to the Sales and Marketing team internally and end users externally. - Manage Customer Visits. Qualifications Required: - Bachelor's degree in Perfusion. - Minimum 1-2 years of experience in the related domain. - Background and experience in the related portfolio. Additional Company Details: You will need to possess excellent verbal and written communication skills, proficiency in MS Office and PowerPoint, public speaking abilities, willingness to travel, and demonstrate a self-driven and team player attitude. Role Overview: You will be responsible for planning, coordinating, and executing clinical programs to promote the concept of ECMO, Counter Pulsation therapy, and Advance Hemodynamics monitoring (AdMon). Additionally, conducting in-service education programs for new and existing users to enhance confidence and maximize the usage of ECMO, IABP, and AdMon will be a key part of your role. Key Responsibilities: - Provide information to Physicians & Allied Health Professionals by discussing/detailing the latest clinical trials. - Conduct in-service education programs for new and existing users to improve confidence and maximize usage of ECMO, IABP, and AdMon. - Offer product support to users through in-person interactions, as well as written or verbal means. - Extend patient support at short notice. - Provide product training to the Sales and Marketing team internally and end users externally. - Manage Customer Visits. Qualifications Required: - Bachelor's degree in Perfusion. - Minimum 1-2 years of experience in the related domain. - Background and experience in the related portfolio. Additional Company Details: You will need to possess excellent verbal and written communication skills, proficiency in MS Office and PowerPoint, public speaking abilities, willingness to travel, and demonstrate a self-driven and team player attitude.

As a Senior Manager IT/Clinical Strategic Sourcing at Fortrea, you will be responsible for leading strategic sourcing initiatives and managing end-to-end Source to Contract processes. Your role will involve collaborating with cross-functional teams to drive value creation and ensure alignment with business objectives. **Key Responsibilities:** - Lead the development, management, and execution of category strategies to support Fortrea's strategic imperatives and mission. - Partner with leaders across the enterprise to provide efficient and effective category strategies and preferred suppliers. - Manage multi-functional stakeholder teams on strategic sourcing initiatives, driving value through supplier relationship management. - Conduct regular contract review meetings with suppliers and key stakeholders to ensure performance meets expectations. - Cultivate a strong team environment and service culture to deliver timely and quality services. - Own and manage the end-to-end Source to Contract process for assigned categories, ensuring compliance and regulatory reporting. - Develop, monitor, and analyze procurement metrics and spend analytics to identify opportunities for improvement. - Conduct market research and analysis to identify potential suppliers and negotiate favorable terms and pricing. - Ensure compliance with company policies, industry regulations, and ethical procurement practices. - Deliver savings and value targets across multiple dimensions, including material deflation and cost optimization. **Qualifications:** - Bachelor's degree in Business Administration, Supply Chain Management, or a related field; MBA preferred. - Deep knowledge of sourcing processes, market trends, benchmarks, and best practices across categories under management. - In-depth knowledge of category strategy, management, and sourcing methodologies. - Proven analytical skills and ability to solve complex problems to drive value. - Strong business and financial acumen with strategic thinking capabilities. - Excellent written and verbal communication skills. - Organizational, time management, and multi-tasking skills. - Working knowledge of data analysis and forecasting tools. - Interpersonal skills and ability to build and maintain trusted relationships. - Attention to detail and accuracy in analysis. - Ability to make decisions and commit to completion dates. - Ability to troubleshoot issues of high complexity. - Proficiency in Microsoft Office365 (Word, Excel, PowerPoint, Outlook, Teams, SharePoint). Fortrea values motivated problem-solvers and creative thinkers who share a passion for overcoming barriers in clinical trials. The company is committed to revolutionizing the development process and delivering life-changing therapies to patients in need. Join Fortrea's exceptional team and be part of a collaborative workspace that nurtures personal growth and enables you to make a meaningful global impact. Visit www.fortrea.com for more information. Fortrea is an Equal Opportunity Employer and is dedicated to creating an inclusive workplace.,

As a Clinical Care specialist, your responsibilities will include: - Diagnosing and managing a wide range of ophthalmic conditions, encompassing medical and surgical disorders. - Performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. - Providing outpatient consultations and inpatient care. - Interpreting diagnostic tests such as OCT, fluorescein angiography, and visual fields. In terms of Leadership & Supervision, you will be expected to: - Lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. - Ensure adherence to high standards of clinical care and patient safety. - Engage in clinical governance activities including audits, morbidity & mortality meetings, and case reviews. Your role will also involve Training & Education aspects, where you will: - Teach and mentor medical students, residents, and other healthcare professionals. - Organize and deliver Continuing Medical Education (CME) sessions. Furthermore, in the domain of Research & Development, your responsibilities will include: - Participating in or leading clinical research activities and trials. - Publishing in peer-reviewed journals and presenting findings at conferences. Additionally, you will have Administrative Duties like: - Contributing to the development of clinical protocols and policies. - Attending departmental meetings and participating in strategic planning. Please note that this is a Part-time position with an expectation of 18 hours per week during the Evening shift, and the work location is In person.,

As an experienced Pattern Maker specializing in knitted kids wear, your primary role will involve developing precise and efficient patterns for children's apparel to ensure optimal fit, quality, and production feasibility. Your proficiency in Richpeace and Gemini CAD software will be crucial for digital pattern development, grading, and marker making. Key Responsibilities: - Develop initial patterns for knitted kids" wear based on designer sketches, specifications, and technical requirements. - Modify and finalize patterns based on sample fittings and technical feedback to meet industry and company standards. - Utilize Richpeace and Gemini CAD software to efficiently create, edit, and grade patterns, as well as convert manual patterns into digital formats. - Collaborate with the sampling team to review garment prototypes, refine patterns, and make necessary adjustments based on fit trials. - Ensure production-friendly patterns, minimizing fabric wastage and optimizing stitching efficiency, while resolving technical issues with sewing, cutting, and quality control teams. - Grade patterns across various sizes following standard kids wear measurement charts to ensure consistency and proper fit. - Maintain detailed pattern files, technical sheets, and necessary documentation for all styles, working in coordination with design and production teams for a smooth workflow. Qualifications: - Strong knowledge of knitted fabrics and their behavior in kids" wear. - Proficiency in Richpeace & Gemini CAD software for pattern making and grading. - Understanding of garment construction, sewing techniques, and fit adjustments. - Ability to create efficient markers to minimize fabric wastage. - Basic knowledge of printing, embroidery placements, and fabric shrinkage calculations. In addition to your technical skills, your role will require strong attention to detail, effective communication, and teamwork skills for seamless coordination with designers, production, and quality teams. Your ability to work under tight deadlines and manage multiple projects simultaneously will be essential. Education and Experience: - Diploma/Degree in Fashion Design, Pattern Making, or a related field. - 2+ years of experience in pattern making for kids" wear, preferably knitted garments. (Note: Expected Salary: 25,000 - 40,000 / Per Month, Timing: 9am - 7pm, Immediate Hiring),

As a technical writer at SyMetric, your role will be crucial in developing comprehensive documentation for the organization's integrated IT Platform for clinical trials. Your responsibilities will include: - Researching, outlining, writing, and editing new and existing content in collaboration with various departments - Independently gathering information from subject matter experts to create procedure manuals, technical specifications, and process documentation - Working with development and support leads to identify documentation repositories, revise and edit content, and determine optimal solutions for data storage - Creating and maintaining information architecture templates that align with organizational and legal standards - Developing content in alternative media forms to enhance usability and maintain a consistent voice across all documentation In this role, your objectives will be to: - Develop documentation that aligns with organizational standards - Gain a deep understanding of products and services to simplify complex information for users - Write user-friendly content that meets the needs of the target audience - Maintain detailed databases of reference materials for research and design purposes - Evaluate current content and propose innovative improvements In terms of qualifications, you should have: - A Bachelor's degree in a relevant technical field such as Computer Science or Healthcare - At least 3 years of experience as a technical writer - The ability to quickly grasp complex topics and effectively communicate them - Experience in writing documentation for various audiences - Strong written and verbal communication skills with attention to detail - Experience collaborating with engineering teams to enhance user experience and create technical support content Additionally, you should possess the following competencies: - Ability to manage multiple projects concurrently and prioritize effectively - Understanding of the systems development life cycle (SDLC) - Previous software development experience - Certification through the Society for Technical Communicators - Proficiency in using XML tools for documentation creation Join SyMetric in Bangalore and contribute to the success of our customer-focused services with your technical writing expertise. As a technical writer at SyMetric, your role will be crucial in developing comprehensive documentation for the organization's integrated IT Platform for clinical trials. Your responsibilities will include: - Researching, outlining, writing, and editing new and existing content in collaboration with various departments - Independently gathering information from subject matter experts to create procedure manuals, technical specifications, and process documentation - Working with development and support leads to identify documentation repositories, revise and edit content, and determine optimal solutions for data storage - Creating and maintaining information architecture templates that align with organizational and legal standards - Developing content in alternative media forms to enhance usability and maintain a consistent voice across all documentation In this role, your objectives will be to: - Develop documentation that aligns with organizational standards - Gain a deep understanding of products and services to simplify complex information for users - Write user-friendly content that meets the needs of the target audience - Maintain detailed databases of reference materials for research and design purposes - Evaluate current content and propose innovative improvements In terms of qualifications, you should have: - A Bachelor's degree in a relevant technical field such as Computer Science or Healthcare - At least 3 years of experience as a technical writer - The ability to quickly grasp complex topics and effectively communicate them - Experience in writing documentation for various audiences - Strong written and verbal communication skills with attention to detail - Experience collaborating with engineering teams to enhance user experience and create technical support content Additionally, you should possess the following competencies: - Ability to manage multiple projects concurrently and prioritize effectively - Understanding of the systems development life cycle (SDLC) - Previous software development experience - Certification through the Society for Technical Communicators - Proficiency in using XML tools for documentation creation Join SyMetric in Bangalore and contribute to the success of our customer-focused services with your technical writing expertise.

As a Sales Executive for Papa Bear - Baby Care Products in Ahmedabad, you will play a crucial role in expanding the reach of our premium Indian brand making clean, safe, and natural baby care products for modern families. Your main responsibilities will include: - Visiting and pitching Papa Bear products to doctors, pediatricians, and dermatologists across Ahmedabad and nearby cities. - Building strong relationships with clinics, hospitals, and distributors to drive product trials. - Ensuring regular follow-ups, order placement, and tracking sales pipeline to achieve monthly targets. - Being the face of Papa Bear in the region to create visibility and trust among healthcare professionals. We are looking for candidates with: - 1 to 5 years of experience in healthcare/pharma/derma sales. - A good network of doctors, pediatricians, or dermatologists in and around Ahmedabad. - Comfort with fieldwork, local travel, and daily doctor meetings. - Energetic, trustworthy, and eager to grow with our purpose-led brand. - Basic English proficiency along with strong local language communication in Gujarati or Hindi. In return, you will receive: - Fixed Salary: 15,000 - 35,000/month (based on experience). - Incentives for closures and doctor activations. - Travel allowance and product training opportunities. - The chance to work with a brand that prioritizes quality and reputation in the healthcare industry. As a Sales Executive for Papa Bear - Baby Care Products in Ahmedabad, you will play a crucial role in expanding the reach of our premium Indian brand making clean, safe, and natural baby care products for modern families. Your main responsibilities will include: - Visiting and pitching Papa Bear products to doctors, pediatricians, and dermatologists across Ahmedabad and nearby cities. - Building strong relationships with clinics, hospitals, and distributors to drive product trials. - Ensuring regular follow-ups, order placement, and tracking sales pipeline to achieve monthly targets. - Being the face of Papa Bear in the region to create visibility and trust among healthcare professionals. We are looking for candidates with: - 1 to 5 years of experience in healthcare/pharma/derma sales. - A good network of doctors, pediatricians, or dermatologists in and around Ahmedabad. - Comfort with fieldwork, local travel, and daily doctor meetings. - Energetic, trustworthy, and eager to grow with our purpose-led brand. - Basic English proficiency along with strong local language communication in Gujarati or Hindi. In return, you will receive: - Fixed Salary: 15,000 - 35,000/month (based on experience). - Incentives for closures and doctor activations. - Travel allowance and product training opportunities. - The chance to work with a brand that prioritizes quality and reputation in the healthcare industry.

As a Clinical Care professional, you will be responsible for diagnosing and managing a wide range of ophthalmic conditions, including medical and surgical disorders. Your role will involve performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. Additionally, you will provide outpatient consultations and inpatient care while interpreting diagnostic tests like OCT, fluorescein angiography, and visual fields. Your leadership and supervision skills will be crucial as you lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. Ensuring high standards of clinical care and patient safety will be a key aspect of your responsibilities. You will also actively participate in clinical governance activities, including audits, morbidity & mortality meetings, and case reviews. In the realm of training and education, you will have the opportunity to teach and mentor medical students, residents, and other healthcare professionals. Organizing and delivering CME (Continuing Medical Education) sessions will be part of your contribution to the growth and development of the healthcare community. Research & Development will be a significant part of your role, where you will participate in or lead clinical research activities and trials. Your findings may be published in peer-reviewed journals, and you will have the chance to present them at conferences, contributing to the advancement of medical knowledge. Additionally, you will be involved in administrative duties, such as contributing to the development of clinical protocols and policies. Attending departmental meetings and engaging in strategic planning will also be part of your responsibilities. Qualifications Required: - Medical degree and relevant board certification - Valid medical license to practice - Experience in ophthalmology, particularly in surgical procedures - Strong leadership and communication skills - Ability to work effectively in a team environment This part-time position requires a commitment of 18 hours per week during the evening shift, with the work location being in person. As a Clinical Care professional, you will be responsible for diagnosing and managing a wide range of ophthalmic conditions, including medical and surgical disorders. Your role will involve performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. Additionally, you will provide outpatient consultations and inpatient care while interpreting diagnostic tests like OCT, fluorescein angiography, and visual fields. Your leadership and supervision skills will be crucial as you lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. Ensuring high standards of clinical care and patient safety will be a key aspect of your responsibilities. You will also actively participate in clinical governance activities, including audits, morbidity & mortality meetings, and case reviews. In the realm of training and education, you will have the opportunity to teach and mentor medical students, residents, and other healthcare professionals. Organizing and delivering CME (Continuing Medical Education) sessions will be part of your contribution to the growth and development of the healthcare community. Research & Development will be a significant part of your role, where you will participate in or lead clinical research activities and trials. Your findings may be published in peer-reviewed journals, and you will have the chance to present them at conferences, contributing to the advancement of medical knowledge. Additionally, you will be involved in administrative duties, such as contributing to the development of clinical protocols and policies. Attending departmental meetings and engaging in strategic planning will also be part of your responsibilities. Qualifications Required: - Medical degree and relevant board certification - Valid medical license to practice - Experience in ophthalmology, particularly in surgical procedures - Strong leadership and communication skills - Ability to work effectively in a team environment This part-time position requires a commitment of 18 hours per week during the evening shift, with the work location being in person.

As a candidate for this position, you will be responsible for designing and developing ladder logic and software for machines. Your key duties and responsibilities will include: - Designs and develops ladder logic / software for Machines. - Demonstrating software sequence and interlocks to customers during machine inspection and trials. - Interfacing electrical systems as per the schedule. - Attending to service calls related to ladder logic / software. - Ensuring that all electrical safety requirements are met while developing machine interlocks / sequence and machine operations. To excel in this role, you should have the following skills and abilities: - Experience in PLC and CNC software. - Proficiency in the usage of NI / Vision Software. Qualifications required for this position include: - BE / Diploma in Electrical and Electronics Engineering or Electronics and Communication Engineering. - At least 4-10 years of experience in developing ladder logic and software for machine tools / SPM. This job will provide you with the opportunity to apply your expertise in PLC and CNC software to design and develop software for various machines.,

You are a motivated and detail-oriented R&D Intern who will be joining our Research & Development team. Your primary responsibilities will include assisting in conducting experiments, analyzing data, supporting innovation projects, and contributing to the development of new products, processes, or technologies. - Support ongoing R&D projects by conducting research, documentation, and technical analysis. - Assist in setting up and conducting laboratory or field experiments if applicable. - Collect, compile, and analyze data from experiments and trials. - Prepare technical reports and presentations for internal reviews. - Collaborate with cross-functional teams such as Product Development, Quality Control, and Manufacturing. - Stay updated with relevant scientific or technological advancements. - Maintain proper records of findings, materials, and procedures. To be eligible for this position, you must have: - Completed a Bachelor's degree in a relevant field such as Cosmetics, Powder Chemist, or Skincare. - Strong analytical and problem-solving skills. - A basic understanding of R&D concepts and techniques. - Proficiency in Microsoft Office (Excel, Word, PowerPoint). - Good written and verbal communication skills. - The ability to work independently and in a team environment. This is a full-time position with a day shift schedule, and the work location is in person.,

Kindly Note This Job for Netherlands Only Location Only Not in India. Major Roles & Responsibilities conducting and supporting scientific investigations and experiments.planning, setting up and undertaking controlled experiments and trials.recording, analysing and interpreting data.demonstrating procedures.collecting, preparing and/or testing samples.maintaining, calibrating, cleaning and testing sterility of the equipment.providing technical support.presenting results to senior staff.writing reports, reviews and summaries.keeping up to date with relevant scientific and technical developments.supervising staff and other laboratory users (such as students).carrying out risk assessments.ordering and maintaining stock and resources.