218 Clinical Supervision Jobs in Chandragiri

As a Clinical Assistant - Obstetrics & Gynecology at the Sir HN RFH, your main responsibility is to assist the Mentor, Director, and Consultants in providing clinical care while adhering to the standards of medical and service excellence. Here are the key responsibilities you will be entrusted with: - Work under the supervision of Mentor, Director, and Consultants to conduct OPD and other clinical activities - Manage casualty cases under the consultants' supervision - Collate and analyze records, reports, and test results to diagnose patients - Prescribe medication, therapy, and specialized medical care under consultation - Explain procedures, obtain consents, and discuss treatments with patients and families - Monitor patients' conditions, reevaluate treatments, and refer to specialists when necessary - Coordinate with OT staff for booking surgeries and follow surgical checklists - Conduct IUCD removals, insertions, deliveries, and other procedures under supervision - Maintain accurate documentation in the Hospital Information System - Coordinate with medical staff for quality care and patient safety - Participate in health programs, quality initiatives, and infection control activities - Ensure optimal resource utilization and cover colleagues when needed - Participate in research, clinical education, and training activities - Adhere to internationally accepted standards of care and infection control protocols In terms of qualifications, you are required to have an MBBS and MS/DNB in Obstetrics & Gynecology, with 3-5 years of post-qualification experience. It is desirable to have experience in a large multispecialty hospital and fellowships in Obstetrics & Gynecology. The core competencies expected from you include putting patients first, striving for excellence, being accountable, showing respect, working in a team, and upholding integrity. You should also possess technical competencies such as knowledge of departmental policies, infection prevention, HIS usage, patient safety, and communication skills. Overall, your role involves providing high-quality clinical care, ensuring patient safety, continuous learning, and contributing to the growth and innovation of the department. As a Clinical Assistant - Obstetrics & Gynecology at the Sir HN RFH, your main responsibility is to assist the Mentor, Director, and Consultants in providing clinical care while adhering to the standards of medical and service excellence. Here are the key responsibilities you will be entrusted with: - Work under the supervision of Mentor, Director, and Consultants to conduct OPD and other clinical activities - Manage casualty cases under the consultants' supervision - Collate and analyze records, reports, and test results to diagnose patients - Prescribe medication, therapy, and specialized medical care under consultation - Explain procedures, obtain consents, and discuss treatments with patients and families - Monitor patients' conditions, reevaluate treatments, and refer to specialists when necessary - Coordinate with OT staff for booking surgeries and follow surgical checklists - Conduct IUCD removals, insertions, deliveries, and other procedures under supervision - Maintain accurate documentation in the Hospital Information System - Coordinate with medical staff for quality care and patient safety - Participate in health programs, quality initiatives, and infection control activities - Ensure optimal resource utilization and cover colleagues when needed - Participate in research, clinical education, and training activities - Adhere to internationally accepted standards of care and infection control protocols In terms of qualifications, you are required to have an MBBS and MS/DNB in Obstetrics & Gynecology, with 3-5 years of post-qualification experience. It is desirable to have experience in a large multispecialty hospital and fellowships in Obstetrics & Gynecology. The core competencies expected from you include putting patients first, striving for excellence, being accountable, showing respect, working in a team, and upholding integrity. You should also possess technical competencies such as knowledge of departmental policies, infection prevention, HIS usage, patient safety, and communication skills. Overall, your role involves providing high-quality clinical care, ensuring patient safety, continuous learning, and contributing to the growth and innovation of the department.

As a Clinical Assistant / Senior Clinical Assistant / Clinical Associate / Senior Clinical Associate in the HPB Surgery & Liver Transplant Department, you will have the following responsibilities and accountabilities: - Maintain a professional approach with all patients, staff, and visitors. - Provide medical cover, both routine and emergency, during duty hours and collaborate with other specialties within the institute. - Adhere to all clinical safety, hygiene, and infection control protocols. - Be available to see patients as needed and participate in teaching programs for postgraduate students. - Identify complex surgical problems and take appropriate action in emergencies with permission from the treating consultant. - Supervise postgraduate students and assist in the daily clinical management of patients under the guidance of Consultants. - Ensure complete patient documentation and obtain consents for surgeries and procedures. - Communicate effectively with patients, families, colleagues, and healthcare workers. - Accompany Consultants for rounds and independently conduct rounds, following up on patient care. - Follow on-call and duty rota as per department requirements. - Participate in Quality Improvement Initiatives and company protocols. - Assist Consultants in the operation theatre and support surgeries under their supervision. Qualifications required: - MBBS, MD/DNB/MS (Specialization as per department's requirement of qualification) - Additional Qualification: Diploma/Fellowship As part of the benefits package, you will receive health insurance and paid time off. This is a full-time, fresher position with in-person work location.,

As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, this role as a Medical Device CRA II could be a great fit for you. As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, thi

As a Mental Health / Wellness Services professional at our Mohali, Punjab location, you will have the following responsibilities: - Work collaboratively with gynecologists, urologists, endocrinologists, and other allied professionals to provide integrated care. - Maintain detailed and confidential client records and documentation as per ethical and legal standards. - Participate in case reviews, supervision, and professional development activities. Please note that this is a full-time, permanent position with a day shift schedule and in-person work location.,

Role Overview: You will be supporting the Study Lead in TCO studies to ensure all trial deliverables are met according to timelines, budget, operational procedures, and quality standards. Additionally, you will assist TCO CSD, CSaD, and CSTL in various tasks related to the management of clinical study materials, development of study tools, guidelines, and training materials. Key Responsibilities: - Develop specific sections of selected study documents and study tools - Manage clinical study material and implement issue resolution plans - Contribute to the preparation of CSR appendices under supervision - Set up and maintain appropriate study tracking forms including enrollment log, site and vendor contact lists, drug shipping logs, and team membership lists - Assist in managing interactions with relevant functions including Global Clinical Supply and Novartis country organizations - Track drug supply at central hubs, local CPOs, and sites, ensuring adequate supply and monitoring expiry dates - Create and maintain HQ TOC, ensure timely completion and maintenance of TMF, and assist in trial data analysis and reporting - Support in meeting scheduling, distribution of meeting agendas/minutes, and archiving of study tools - Track PK and biomarker sample tracking, act as a liaison with sites for sample shipment and reconciliation - Assist in financial management, forecasting, and vendor management activities - Support other ClinOps functions as required Qualifications Required: - Prior experience in clinical trial operations or related field - Strong organizational and multitasking skills - Excellent communication and collaboration abilities - Familiarity with drug tracking and supply management - Proficiency in data analysis and reporting - Ability to work effectively in a fast-paced environment with attention to detail Please note that Novartis is committed to providing reasonable accommodation to individuals with disabilities if needed during the recruitment process. Additionally, the company values diversity and inclusivity in the work environment to better serve patients and communities.,

As a Lecturer in Clinical Pharmacologists at Charkos College of Nursing in Mysuru, your primary role involves teaching and conducting research in the field of studying drugs in humans. You will be responsible for delivering engaging lectures, tutorials, and practical sessions on clinical and experimental pharmacology. Additionally, you will supervise research projects, provide guidance to students, and contribute to curriculum development. Key Responsibilities: - Deliver lectures and tutorials on clinical and experimental pharmacology - Conduct practical sessions to enhance student understanding - Supervise research projects and dissertations, offering guidance and mentorship Qualifications Required: - M.Sc in Pharmacology Please note that no additional details about the company were provided in the job description. As a Lecturer in Clinical Pharmacologists at Charkos College of Nursing in Mysuru, your primary role involves teaching and conducting research in the field of studying drugs in humans. You will be responsible for delivering engaging lectures, tutorials, and practical sessions on clinical and experimental pharmacology. Additionally, you will supervise research projects, provide guidance to students, and contribute to curriculum development. Key Responsibilities: - Deliver lectures and tutorials on clinical and experimental pharmacology - Conduct practical sessions to enhance student understanding - Supervise research projects and dissertations, offering guidance and mentorship Qualifications Required: - M.Sc in Pharmacology Please note that no additional details about the company were provided in the job description.

As a Psychology Training and Internship candidate at Lissun, you will have the opportunity to gain practical experience in the field of mental health, focusing on Child Psychology, Organizational Psychology, and Neurorehabilitation. Your responsibilities will include: - Assisting in conducting psychological assessments - Administering standardized psychological tests - Providing psychological support under professional supervision - Contributing to mental health education initiatives through workshops and awareness sessions - Supporting communication and outreach efforts to promote mental well-being Qualifications required for this role include: - Knowledge in Psychology and Mental Health - Strong skills in Communication and Education - Understanding of Mental Health principles - Ability to work independently and in a team - Pursuing or completed a degree in Psychology or a related field - Students of all semesters are eligible - Prior experience in mental health settings is a plus Lissun is a tech-enabled mental health startup that specializes in providing support to individuals for their mental and emotional wellness needs. Additionally, Lissun offers tailored EAP solutions powered by AI to companies, transforming workplace mental health into a competitive advantage. With over 150 therapists in more than 20 cities, Lissun collaborates with forward-thinking companies to create thriving workplaces with happier employees. By investing in genuine mental health support with Lissun, companies can experience a significant increase in productivity and engagement.,

Excelya, one of the leading independent CRO in Europe, is a people-centered Contract Research Organization (CRO) committed to providing a personal and authentic experience within a young, ambitious health company. With a team of 900 Excelyates, we are on the path to becoming the clinical research leader in Europe. Our unique one-stop provider service model offers full-service, functional service provider, and consulting, allowing our Excelyates to evolve through a diverse array of projects. We collaborate with preeminent experts to advance scientific, managerial, and human knowledge for the improvement of the patient journey. As a Clinical Data Manager with Excelya, you will be responsible for performing Data Management tasks per client work orders to high regulatory standards and Clients SOPs. You will deeply acknowledge and strictly follow applicable Excelya and Clients SOPs, working under the supervision of more senior staff. Your responsibilities will include data cleaning, data review, discrepancy management, data reconciliation activities, generating study metrics and status reports, participating in study documentation archiving, and may be involved in EDC database build and testing through go-live. Additionally, you will complete administrative tasks as required and undertake other assigned tasks within the Excelya Group companies. Key Responsibilities: - Acknowledge and strictly follow applicable Excelya and Clients SOPs - Work under the supervision of more senior staff - Perform data cleaning, data review, discrepancy management, and data reconciliation activities - Collaborate with the Lead Data Manager for the study - Generate study metrics and status reports - Participate in study documentation archiving - May be involved in EDC database build and testing - Complete Excelya administrative tasks as required Qualifications Required: - Holds a Bachelor's degree qualification in a Scientific discipline - 1 or more years as a Data Manager or equivalent combination of education, training, and experience - Knowledge and understanding of ICH GCP and other relevant guidelines - Experience in clinical trial databases, data flow, and eCRF design - Proficient in computer technology - Effective verbal and written communication skills - Fluent in local language and English,

Job Description Role Overview: You will be joining Athulya Senior Care in Chennai as a full-time MD Geriatrician. Your primary responsibility will involve providing medical care and comprehensive assessments to elderly patients. You will be tasked with developing individualized care plans, managing chronic conditions, and collaborating with interdisciplinary teams to ensure holistic senior care. Additionally, you will supervise clinical staff, communicate effectively with patients and families, and maintain accurate medical records. Key Responsibilities: - Provide medical care and comprehensive assessments to elderly patients - Develop individualized care plans and manage chronic conditions - Coordinate with interdisciplinary teams for holistic senior care - Supervise clinical staff and maintain accurate medical records - Communicate effectively with patients and families Qualifications: - Expertise in Geriatric Medicine, including diagnosis, treatment, and management of age-related health conditions - Strong clinical skills in chronic disease management, preventive care, and rehabilitation for seniors - Ability to collaborate with interdisciplinary teams, including nurses, physiotherapists, and caregivers - Experience in patient communication, medication management, and clinical supervision - MD in Geriatric Medicine (or equivalent) and state medical licensure - Strong organizational and problem-solving abilities - Familiarity with using healthcare technology and electronic medical records (EMRs) - Compassion, patience, and a commitment to improving the quality of life for seniors Job Description Role Overview: You will be joining Athulya Senior Care in Chennai as a full-time MD Geriatrician. Your primary responsibility will involve providing medical care and comprehensive assessments to elderly patients. You will be tasked with developing individualized care plans, managing chronic conditions, and collaborating with interdisciplinary teams to ensure holistic senior care. Additionally, you will supervise clinical staff, communicate effectively with patients and families, and maintain accurate medical records. Key Responsibilities: - Provide medical care and comprehensive assessments to elderly patients - Develop individualized care plans and manage chronic conditions - Coordinate with interdisciplinary teams for holistic senior care - Supervise clinical staff and maintain accurate medical records - Communicate effectively with patients and families Qualifications: - Expertise in Geriatric Medicine, including diagnosis, treatment, and management of age-related health conditions - Strong clinical skills in chronic disease management, preventive care, and rehabilitation for seniors - Ability to collaborate with interdisciplinary teams, including nurses, physiotherapists, and caregivers - Experience in patient communication, medication management, and clinical supervision - MD in Geriatric Medicine (or equivalent) and state medical licensure - Strong organizational and problem-solving abilities - Familiarity with using healthcare technology and electronic medical records (EMRs) - Compassion, patience, and a commitment to improving the quality of life for seniors

As an Adjunct Clinical Psychology Faculty member at the Institute for the Psychological Sciences (IPS) at Divine Mercy University (DMU) in Sterling, VA, your role will involve various tasks within the PsyD Program. You will be responsible for teaching assigned coursework, providing clinical supervision to students, offering dissertation advising, engaging in research and scholarship activities, and potentially handling administrative duties. The IPS doctoral program in clinical psychology is accredited by the APA and offers a distinctive integration of psychological science with the Catholic understanding of individuals, marriage, and family. Key Responsibilities: - Teach assigned coursework in the doctoral program - Provide clinical supervision to students - Offer dissertation advising - Engage in research and scholarship activities - Potentially handle administrative duties Qualifications Required: - Possess a doctoral degree in psychology from a regionally accredited institution - Have experience teaching at the graduate level in areas such as Child, Marriage, and Family Therapy, Psychological Assessment, Dialectical Behavior Therapy, or Basic clinical skills courses emphasizing empathy and attachment - Demonstrate recent relevant work in the field through teaching, research, publications, or clinical practice - Hold current licensure or immediate license eligibility as a clinical psychologist in the Commonwealth of Virginia The ideal candidate for this role at IPS/DMU would be a graduate of a regionally accredited program, have teaching experience in similar clinical psychology programs, specialize in one of the mentioned areas, exhibit ongoing research and scholarship, and display a desire and ability to teach and supervise students in line with the DMU/IPS mission. Candidates with strong clinical training, supervision, and teaching skills will also be considered, even without a significant academic track record. The appointment rank and salary will be based on qualifications. To apply for this position, please submit the following: - Current curriculum vitae - Official transcripts for all post-secondary education - A list of references from three higher education professionals - Cover letter addressing your compatibility with the DMU/IPS mission The review of applications will commence immediately and will continue until the position is filled. IPS at Divine Mercy University is an Equal Opportunity Employer dedicated to enhancing diversity within its community. The university seeks candidates who exhibit openness and respect for the Roman Catholic Church and its institutions and who are genuinely interested in advancing DMU's mission within the Church.,

Role Overview: As a member of the Medical Staff department in Mumbai, you will need to maintain a professional approach with all patients, staff, and visitors. Your responsibilities will include providing medical cover, both routine and emergency, collaborating with other specialties, and adhering to clinical safety, hygiene, and infection control protocols. Additionally, you will be required to participate in teaching programs for postgraduate students, assist consultants in the operation theatre, supervise postgraduate students, manage patients" clinical care, ensure complete documentation, and communicate effectively with various stakeholders. Key Responsibilities: - Provide medical cover, both routine and emergency, during scheduled hours - Adhere to clinical safety, hygiene, and infection control protocols - Participate in teaching programs for postgraduate students - Assist consultants in the operation theatre and surgeries under supervision - Supervise postgraduate students and ensure proper patient care - Manage daily clinical management of patients in collaboration with RMOs and Consultants - Ensure complete and accurate patient documentation - Communicate effectively with patients, family, colleagues, and other healthcare workers - Accompany Consultants for rounds and take independent rounds as necessary - Follow on-call and duty rota based on department requirements - Contribute to the Quality Improvement Initiative & protocols of the company Qualifications Required: - MBBS degree - MD/DNB/MS with specialization as per the department's requirements Company Details: The JD does not contain any additional details about the company.,

As a Clinical Assistant - Ophthalmology at our organization, your main responsibility will be to assist the Director and Consultants in diagnosing and delivering clinical care in accordance with the Sir HN RFH standards of medical and service excellence. You will work under the supervision of the Director/Consultants and perform a variety of tasks to ensure the well-being of patients. Some of your key responsibilities include: - Assisting in conducting OPD and other clinical activities as specified - Conducting free OPDs and Executive Health Check-ups under supervision - Managing casualty cases under supervision - Collating and analyzing records, reports, and test results to diagnose diseases - Prescribing or administering medication, therapy, and other specialized medical care - Explaining procedures, obtaining consents, and discussing test results or treatments with patients and their families - Monitoring patients" conditions, reevaluating treatments as necessary, and referring patients to specialists when required - Coordinating with various departments for booking OT, ensuring availability of surgical requirements, and following surgical checklists - Maintaining and updating documentation in the Hospital Information System - Coordinating activities of medical staff for quality care and patient safety - Participating in health programs, outreach activities, or communities for prevention and treatment of injuries or illnesses - Ensuring clinical care and infection control quality indicators are within defined benchmarks - Actively participating in quality programs and infection control activities - Ensuring optimum utilization of departmental resources - Mentoring and guiding junior medical staff and DNB students - Participating in clinical education, research, and advancing the practice of medicine - Attending conferences, presenting, and updating knowledge and skills - Providing feedback to improve departmental services and growth In terms of qualifications, you should have MBBS and MS Ophthalmology or MS/DNB (results awaited). Experience of 0-3 years post MS/DNB in Ophthalmology is necessary, with experience in a large multispecialty hospital being desirable. Additional certifications or fellowships in Ophthalmology would be advantageous. Your competencies should align with the core values of Patient First, Excellence, Accountability, Respect, Teamwork, and Integrity. You should also possess technical competencies such as knowledge of departmental policies, teaching, research, infection prevention and control, JCI & NABH standards, HIS usage, patient safety, and communication skills. Overall, as a Clinical Assistant - Ophthalmology, you will play a crucial role in providing high-quality clinical care, ensuring patient safety, and contributing to the growth and excellence of the department.,

As a Clinical Sales Specialist at Medtronic, you will be responsible for conducting on-site education and consulting, supporting field personnel to ensure the best outcomes for Medtronic customers, and partnering with sales colleagues to develop and execute sales plans within one or more business units. You will also participate in conventions, forums, and meetings to increase product awareness, work closely with the Clinical Lead, Clinical Management, and Regional Sales team to provide customer case and sales support, and identify and execute growth opportunities with the Sales and Clinical Support Team. Additionally, you will serve as a technical resource to support sales of a specific medical product or solution. Key Responsibilities: - Conduct on-site education and consulting - Support field personnel in providing the best outcomes for customers - Develop and execute sales plans with sales colleagues - Participate in conventions, forums, and meetings to increase product awareness - Work closely with Clinical Lead, Clinical Management, and Regional Sales team to provide customer case and sales support - Identify and execute growth opportunities with Sales and Clinical Support Team - Serve as a technical resource to support sales of a specific medical product or solution Qualifications Required: - Minimum of 4 years relevant experience - Broad theoretical job knowledge typically obtained through advanced education At Medtronic, you will have the opportunity to work on smaller, less complex projects or related activities as an individual contributor. You will have the autonomy to work on a project or team with close supervision, identifying and addressing problems that are not immediately evident. Additionally, you will communicate primarily with internal contacts within your immediate group and make minor changes in systems and processes to solve problems. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Medtronic offers a competitive Salary and flexible Benefits Package. The company values its employees" contributions and offers a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. At Medtronic, the mission is to alleviate pain, restore health, and extend life by boldly attacking the most challenging health problems facing humanity. The company unites a global team of 95,000+ passionate individuals who are engineers at heart, working together to engineer real solutions for real people. Medtronic encourages diversity and is committed to creating innovative healthcare technology solutions.,

As an experienced and motivated Medical Physicist in the Varian India Zone team, your role will involve providing clinical training, application support, and subject matter expertise to customers, both on-site and remotely. You will ensure the safe and effective use of Varian technologies, enabling customers to optimize clinical workflows and leverage the full capabilities of advanced solutions to meet their operational and patient care goals. **Key Responsibilities:** - Train, counsel, and support customers in adapting their work procedures and propose new approaches following the installation or implementation of new or upgraded products. - Develop tailored training programs for customers on the appropriate use of Varian hardware and software products. - Deliver high-quality on-site or remote training to customers, instructing them on newly installed products, upgrades to existing systems, or other product developments. - Provide application support for internal product testing activities and participate in Customer Satisfaction Phase testing as needed. - Offer occasional application support for Education, Sales, or Marketing teams, such as Clinical School assistance or customer demonstration support. - Provide demonstration support at local, regional, and national customer trade events as required. - Support and participate in the internal training of colleagues when necessary. - Maintain up-to-date records and handle day-to-day administrative tasks, including timesheets, expense reports, and training reports (as applicable), to ensure accurate and current company data on customer-oriented activities. - Continuously maintain competencies and complete organizational training in a timely manner, such as Learn4U certifications, internal or external training courses, or on-site hospital visits. - Attend Health & Safety training to acquire and maintain a strong understanding of national laws and organizational regulations related to workplace health and safety, with a particular focus on travel safety, radiation safety, and electrical safety, and apply this knowledge systematically. **Qualification Required:** - Fluency in English (both spoken and written). - Willingness to travel extensively within India, Bangladesh, Nepal, and Sri Lanka, including during normal and non-standard hours and days as required to provide optimal support. - Excellent communication skills: teaching or training experience is a plus. - 3-4 years of professional clinical experience in radiotherapy, with expertise in Varian Products such as Oncology Information Systems (ARIA) and Treatment Planning Systems (Eclipse). - Proficiency in Microsoft Windows and Office applications. - Strong understanding of customers" clinical needs and requirements. - Exceptional communication and organizational skills, coupled with a mature and professional approach. - In-depth knowledge of modern radiotherapy techniques and their underlying principles. - Solid understanding of processes and methodologies related to Varian product areas, including product specification, development, expansion, security, and safety. - High level of self-motivation and the ability to work independently with minimal supervision while maintaining effective collaboration with the broader team. - Comfort with working within a horizontal organizational structure. - Masters degree (MSc) in Medical Physics or a Postgraduate Diploma in Radiological Physics, with 3-4 years of relevant experience.,

As an Optometrist at our company, your role involves performing various orthoptic workups for asthenopia patients and conducting specific tests for patients with near vision complaints. You will be responsible for performing D15 for pre-employment ophthalmic evaluations and utilizing instruments such as Perimetry, pachymetry, and A-scan/B-scan/OCT as per standard operating procedures. It is crucial to document all ophthalmic workups accurately in separate worksheets and ensure the correctness, completeness, and timely completion of each workup. Key Responsibilities: - Perform orthoptic workups for asthenopia patients - Conduct Flipper Test for non-presbyopia patients with near vision complaints - Perform D15 for pre-employment ophthalmic evaluations - Utilize instruments like Perimetry, pachymetry, and A-scan/B-scan/OCT - Document all ophthalmic workups accurately - Maintain and monitor correctness, completeness, and timeliness of workups - Inform higher authorities of any mechanical malfunctions - Conduct contact lens and LVD workups under supervision - Counsel patients during emergencies and follow patient counseling protocols - Sign name, date, and time on each case paper - Attend CME lectures, follow SOPs, and handle assigned responsibilities Qualification Required: - Degree in Optometry In addition to the responsibilities and qualifications outlined above, you will benefit from food provision, health insurance, paid sick time, and Provident Fund. The work schedule includes day, evening, morning, and rotational shifts with a yearly bonus. Please note that this is a full-time, permanent position suitable for freshers with a preference for candidates with 1 year of relevant work experience. The work location is in person.,

You have a strong interest in clinical research and drug development. You have a basic understanding of Good Clinical Practice (GCP) and clinical trial processes, and you are open to receiving training in these areas. Your attention to detail, communication, and organizational skills are excellent. You are able to manage your time effectively and thrive in a team environment. - Support the initiation, monitoring, and close-out of clinical trial sites under supervision. - Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements. - Basic understanding of Good Clinical Practice (GCP) and clinical trial processes - Excellent attention to detail, communication, and organizational skills - Ability to manage time effectively and work in a team environment The company offers paid sick time, performance bonus, and yearly bonus. The work location is in person.,

As a Junior Project Manager, your role will involve supporting the planning, coordination, and monitoring of clinical research projects from initiation to completion. This will include hands-on execution tasks such as preparing study documents, coordinating with clinical sites, assisting with data collection and monitoring, and contributing to scientific writing. Additionally, periodic travel to clinical sites for training, data collection, and monitoring activities will be required. Key Responsibilities: - Assist in planning, execution, and monitoring of ongoing and upcoming clinical studies - Prepare and maintain clinical documentation including study protocols, informed consent forms, IRB submissions, CRFs, SAP, and ensure compliance with GCP/ICH and ISO 14155 - Coordinate communication between study sites, investigators, and internal teams - Participate in site selection, initiation, training, monitoring visits, and close out to ensure protocol adherence and drive enrollment using risk-based strategies - Implement data quality controls across EDCs and imaging - Maintain audit readiness with CAPA management and SOP stewardship aligned to the QMS - Track study progress, data entry, and milestones; flag any deviations or delays - Support data management and quality assurance activities - Assist in scientific and regulatory writing as required, including preparation of study reports, abstracts, and manuscripts - Maintain compliance with regulatory, ethical, and QMS requirements - Support orientation and supervision of interns or clinical technicians involved in research activities Technical Competencies: - Good understanding of clinical research methodology and ethical practices - Exposure to protocol writing, IRB documentation, and data management preferred - Strong documentation, organizational, and analytical skills - Proficiency in Microsoft Office tools (Word, Excel, PowerPoint) - Basic understanding of statistical analysis is an advantage - Excellent written and verbal communication skills Behavioral Competencies: - Strong attention to detail and proactive problem-solving mindset - Excellent interpersonal and coordination skills - Ability to multitask and manage time effectively - Collaborative team player with a willingness to learn - High degree of professionalism and accountability Other Requirements: - Willingness to travel up to 30% for site visits, training, and data collection - Immediate joiners preferred,

As a Data Analyst at Agilisium, your role will involve gathering, validating, and analyzing data from clinical, operational, and administrative systems. You will be responsible for building interactive reports and dashboards using tools like Power BI, Tableau, or similar platforms to present insights to leadership and stakeholders. Additionally, you will generate routine and ad hoc analytical outputs to support business decisions and performance reviews. Key Responsibilities: - Gather, validate, and analyze data from various systems - Build interactive reports and dashboards using Power BI, Tableau, or similar tools - Generate routine and ad hoc analytical outputs - Develop and monitor Key Performance Indicators (KPIs) and operational metrics - Identify performance trends and provide actionable insights - Support clinical operations and research teams by analyzing data related to study execution, patient enrollment, and protocol adherence - Partner with cross-functional teams to evaluate workflows and recommend process improvements Qualifications & Skills: - Bachelors or Masters degree in Life Sciences, Healthcare, Statistics, Data Analytics, or related discipline - 4-6 years of experience in data analytics within clinical operations, clinical research, or healthcare domains - Strong proficiency in data visualization tools such as Power BI, Tableau, or Qlik - Proficient in querying languages like SQL (Python or R is a plus) - Solid understanding of clinical operations processes, KPIs, and research data frameworks - Excellent analytical, problem-solving, and storytelling skills - Effective communicator with the ability to translate data insights into business actions - Ability to work independently with minimal supervision while collaborating across diverse teams - Deep expertise/experience with CTMS (not EDC) About Agilisium: Agilisium is the Life Sciences industry's premier Autonomous Agentic AI and Applied AI Services Company. They specialize in developing AI-engineered business processes that are autonomous, scalable, and purpose-built for Life Sciences. Agilisium has been recognized for their expertise and growth by organizations such as Everest Group, Inc. 5000, and AWS. They continue to invest in top-tier talent to drive innovation and impact across the Life Sciences value chain. Learn more: [www.agilisium.com](www.agilisium.com),

As a Clinical Operations Manager/Senior Clinical Operations Manager at Novotech, you will play a crucial role in supervising, leading, and managing the Clinical operation team to ensure the successful conduct of clinical trials in adherence to ICH-GCP guidelines, local regulatory requirements, Novotech/client SOPs, and the Project Agreement. Key Responsibilities: - Act as the Novotech ambassador for the India team, leading discussions on India Clinical services capabilities in BDM and client meetings. - Drive new business for Novotech India Clinical Services in collaboration with Business Development. - Serve as a line manager for assigned CRAs, IHCRAs, RSAs, and mentor clinical operations staff. - Conduct regular meetings with line reports to review workload, welfare, and developmental needs. - Set written goals, perform annual appraisal interviews, and submit promotion requests as necessary. - Ensure alignment of resources and recruitment, participate in interviews for potential new hires. - Collaborate with Clinical Operations management team, Learning and Development, and CRAs to address individual learning requirements. - Participate in departmental activities, present at clinical team meetings, attend company meetings, and contribute to the development of clinical processes and SOPs. - Maintain staff utilisation levels, review and approve timesheets of direct reports. - Facilitate local project delivery by understanding regional project objectives and working alongside line reports. - Conduct monitoring assessments and visits to ensure compliance with SOPs, ICH-GCP guidelines, and local regulatory requirements. - Establish and nurture relationships with key clinical trial sites and opinion leaders. Qualifications Required: - Graduate in a clinical or life-sciences related field or have line management experience in the pharmaceutical industry. - Minimum 7 years of experience in clinical research with significant monitoring experience as a CRA/SCRA or similar role. - At least 3 years of line and/or matrix management experience within the CRO industry.,

As a Medical Writer II (Clinical Trial Transparency) at Syneos Health, you will play a crucial role in compiling, writing, and editing medical writing deliverables. Your responsibilities will include mentoring less experienced medical writers, developing various documents such as clinical study protocols, clinical study reports, patient narratives, annual reports, and investigator brochures with minimal supervision. - Review statistical analysis plans and table/figure/listing specifications for content, grammar, format, and consistency. - Collaborate with department heads and staff in data management, biostatistics, regulatory affairs, and medical affairs to produce high-quality writing deliverables. - Serve as a peer reviewer to ensure scientific content accuracy, clarity, overall consistency, and proper format. Adherence to established regulatory standards, including ICH-E3 guidelines, Company Standard Operating Procedures, and client standards is paramount. Your role will involve performing online clinical literature searches, maintaining a working knowledge of the drug development process and regulatory guidelines, and continuing professional development to stay informed about regulatory guidance affecting medical writing. To qualify for this position: - Bachelor of Science degree with relevant writing experience or a Bachelor of Arts degree in Social Sciences, English, or Communications with scientific and/or medical knowledge. - Proficiency in English grammar, FDA and ICH regulations, and familiarity with AMA style guide is necessary. - Effective presentation, proofreading, interpersonal, and leadership skills are essential for this role, along with a team-oriented approach. If you are passionate about making a meaningful impact in the field of medical writing and are eager to contribute to the development of cutting-edge therapies, Syneos Health offers a dynamic and supportive work environment where your contributions will be valued and recognized. Join us in our mission to accelerate customer success and transform lives through innovative medical writing practices.,