8317 Clinical Research Jobs - Page 24

Support the setup, administration, and maintenance of electronic Trial Master File (eTMF), IMPACT CTMS/eSTRA, and related clinical tools. Assist in project setup from initiation to closure, including site document collection, archiving, and quality control. Maintain study portals, version-controlled documents, and e-training records. Track project timelines and milestones, providing progress reports. Draft, update, and maintain key study documentation, SOPs, manuals, and training guides. Conduct file reviews and support internal/external audits to ensure document completeness and regulatory compliance. Job Requirements Bachelor's degree in Life Sciences, Pharmacy, or a related field. Possess...

Review scales administered by raters to ensure standardized assessments. Conduct live interactions with raters to discuss methodology, scoring techniques, and provide guidance. Evaluate rater performance through mock interviews or functional assessments. Prepare for discussions with raters by evaluating case data and relevant scale items. Complete assigned rater interactions and tasks as scheduled. Submit documentation associated with tasks in a timely manner. Participate in orientation, training, and calibration activities. Maintain strong interpersonal skills to interact professionally with all levels of personnel and clients, providing guidance and feedback to ensure data reliability and ...

Participate in all required orientation, training, and calibration activities. Evaluate case data and prepare for rater discussions by reviewing scale items and preparing relevant documents. Conduct rater interactions and complete assigned tasks on schedule. Ensure timely submission of all documentation related to assigned tasks. Provide functional assessments of rater performance and assist with trial communications. Collaborate with cross-functional teams to achieve project goals. Job Requirements Minimum Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work; MD, DO, or PhD preferred. Minimum 3 years of experience administering psychiatric assessments, rati...

Participate in all required orientation, training, and calibration activities. Review case data and prepare for discussions with raters, including understanding scale items and having necessary documents ready. Conduct rater interactions and complete assigned tasks according to schedule. Submit all required documentation on time. Administer psychiatric assessments, rating scales, or structured clinical interviews as part of the role. Engage in functional assessments such as mock interviews. Job Requirements Minimum Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work; MD, DO, or PhD preferred. Minimum 3 years administering psychiatric assessments, rating sca...

Contribute to Clinical Development Plans (CDP), product value propositions (TVP), and market access strategies in collaboration with relevant functions. Provide medical input and support across all activities related to clinical studies, including medical training, feasibility, data review, and stakeholder communications. Oversee the medical review of clinical trial data, safety event assessments, and coding of events and drugs. Develop and amend clinical protocols and informed consent documents. Prepare and review key clinical documents, such as Clinical Study Reports, Investigator Brochures, and Clinical Trial Authorization dossiers. Collaborate closely with internal and external stakehold...

Manage clinical trials from initiation to closeout, ensuring compliance with regulatory requirements and ICH GCP guidelines. Conduct site feasibility assessments and negotiate study budgets with sites. Ensure timely execution of clinical trial agreements and oversee site invoicing. Provide periodic updates on study progress, risks, and deliverables to stakeholders. Lead communication with cross-functional units to ensure efficient study conduct. Manage IMP supplies at sites and coordinate resupply orders. Ensure recruitment and retention strategies at sites are on track and mitigate study recruitment risks. Ensure compliance with PD & SAE reporting, audits, and inspections, performing site c...

Oversee country and site selection, working with the Registries and Local Medical Affairs teams. Organize study materials, ethical and regulatory submissions, and ensure contracts and financial agreements. Maintain oversight of Registries, coordinate with Clinical Research Associates (CRAs), monitor contract issues, and track data quality. Ensure safety reporting and quality control, implementing Corrective and Preventive Actions (CAPA) as needed. Communicate effectively with stakeholders, providing updates and resolving issues promptly. Contribute to TMF compliance and maintain study tracking tools. Job Requirements A degree in Pharma or a scientific Life science discipline is required. Str...

Manage, mentor, and develop a team of clinical safety professionals. Cultivate and maintain strong relationships with clients and internal stakeholders by providing expert safety knowledge. Oversee clinical safety case management and aggregate reporting responsibilities for direct reports to meet client expectations with high quality. Create safety management plans tailored to client needs. Provide safety review of clinical study documents, including protocols, study reports, and marketing application components. Develop and implement effective safety strategies to ensure the safety of clinical trials. Job Requirements Bachelor's degree in a healthcare-related field (Nursing, Pharmacy, Pharm...

Medblue Innovations Private Limited is looking for Regulatory Specialist to join our dynamic team and embark on a rewarding career journey We are looking for skilled Regulatory Specialists to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with relevant laws and regulations. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Conduct thorough reviews of regulatory documents and submissions. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Provide expert guidance on regulatory matters to intern...

Medblue Innovations Private Limited is looking for Clinical Trial Coordinator to join our dynamic team and embark on a rewarding career journey We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Manage study timelines, budgets, and resources to meet pr...

We are seeking an experienced Executive to join our RD division This role will contribute to the company's success by providing leadership and strategic oversight of research initiatives, fostering innovation, and driving the development of cutting-edge products and solutions As an Executive, you will leverage your extensive knowledge of RD processes and industry trends to make strategic decisions that propel our organization forward You will collaborate with cross-functional teams, including researchers, scientists, and engineers, to identify and prioritize research directions, assess the feasibility of new ideas, and align efforts with business goals 1. Should be able to handle a reactions...

We are looking for a highly skilled and experienced Regulatory Affairs professional to join our team at Niva Bupa Health Insurance. The ideal candidate will have a strong background in regulatory affairs and excellent analytical skills. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze and interpret complex regulations to identify opportunities and challenges. Prepare and submit regulatory documents to relevant authorities. Monitor and report on regulatory changes that may impact the organization. Provide training and guidance to staff on regul...

We are looking for a highly skilled and experienced ABDM-SME to join our team at Niva Bupa Health Insurance. The ideal candidate will have a strong background in sales and marketing, with excellent communication and interpersonal skills. Roles and Responsibility Develop and implement effective sales strategies to achieve business objectives. Build and maintain strong relationships with clients and stakeholders. Conduct market research and analyze industry trends to identify new business opportunities. Collaborate with cross-functional teams to drive business growth. Provide exceptional customer service and support to clients. Identify and mitigate risks associated with business operations. J...

Role Overview The Anatomist will support product development across all modules of Cadaviz, including Gross Anatomy, Regional Anatomy, Histology, Embryology, Neuroanatomy, and all dissection-related structures. Key Responsibilities Serve as the primary Anatomical Subject Matter Expert for Cadaviz. Validate CAD-based anatomical models with the 3D development team. Provide guidance on organs, muscles, nerve pathways, bony landmarks, and dissection planes. Interpret human and animal cadaver data for model refinement. Review and validate prosection datasets. Prepare curriculum-aligned content: clinical cases, modules, histology & embryology explainers. Prepare quizzes and assessments. Source hig...

Senior Clinical Research Associate (Sr. CRA) Location: Ahmedabad (Hybrid) Experience: 56 years (Mandatory oncology monitoring experience) Qualification: Masters in Life Sciences / M.Pharm / Pharm D Job Description We are hiring an experienced Senior Clinical Research Associate with strong hands-on site monitoring experience in oncology clinical trials . The role involves end-to-end site management, monitoring, documentation, and ensuring study compliance as per GCP, NDCTR 2019, SOPs, and protocol. Key Responsibilities Conduct SQV, SIV, IMV, closeout visits, and pre-audit visits. Perform end-to-end site management ensuring protocol, GCP, and regulatory compliance. Perform SDV/SDR, review CRFs...

Job Title: eTMF Executive Business Unit: Clinical Research Location: Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” TASKS AND RESPONSIBILITIES: Documentation and Administrative Support: Ensuring all trial-...

Job Description: Deputy Head of Clinical Operations (Deputy HCO) Educational Qualifications 1. B.Sc. Nursing + MHA preferred OR 2. Masters degree in nursing, Public Health, Healthcare Management, or relevant field 3. 9-10 years’ experience in senior nursing or clinical operations roles (Nursing Superintendent- level preferred). Key Responsibilities A. Clinical Oversight & Rounds 1. Conduct daily clinical rounds across facilities and report HCO with report 2. Review resident condition, nursing care quality, medication practices, infection control protocols. 3. Ensure timely escalation to HCO and treating doctors. 4. Monitor care for dementia, behavioural symptoms, chronic illnesses, and post-...

Job Title: Clinical Trial Assistant Business Unit: Clinical Research Location: Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” TASKS AND RESPONSIBILITIES: Documentation and Administrative Support: Assist in...

Job Title: Clinical Data Manager (CDM) JD For Clinical Data Manager (CDM): Job Location: Hyderabad / Kakinada Experience: 4 to 8 years Role & responsibilities Supports Clinical Data Manager (CDM) for assigned studies with the planning, execution and management of clinical trials. The CDA is responsible for the following activities with CDM support/oversight: Supports Sr.CDM with Data Management activities, including oversight of outsourced activities to CRO and other third-party vendors Supporting Sr.CDM in collection, tracking, and maintenance of data management documentation for the electronic Trial Master File (eTMF). Accountable for the data quality and data integrity for pivotal clinica...

Must have experience in any of the EHR platforms (Nextgen, Epic, Athena, eClinicalWorks, Dr.Chrono, Cerner, Medent, Veradigm) Analyze patient medical information on EHR platforms. Enter & update patient data accurately based on predefined rules. Required Candidate profile Good verbal communication skills, may have to communicate with US team members Ability to perform repetitive tasks with consistency Willing to work in night shift (8 PM to 4 AM) Cab will be provided

Solution Design and Architecture: Design integration architectures within larger products modules. Improve re-usability by looking for reusing less amount of different components for the same purpose, standardizing over less, "better" ones. Help in selecting the best module for a specific use-case. Analyze the current tech composition and suggest ways for improving it by adhering to Architects team principles. Technical Advisement: Act as a primary technical advisor to development teams, providing insights on how various solutions can be customized and integrated. Research on new technologies and modules and test their suitability for the purpose. Build First of Kind implementations (PoC) an...

As a Project Training Coordinator at Covance in Bangalore, India, your role will involve: - Facilitating the creation, revision, or inactivation of all project training requirements in the LMS. - Providing regular updates to project leaders and project coordinators on the status of project-related training requirements. - Monitoring and tracking compliance of study teams to training requirements using LMS reporting capabilities and Excel. - Sending out notifications to team members who are delinquent in completing training requirements. - Escalating repeated delinquent training requirements to project leads. - Assigning and removing role-based curricula to staff members throughout the study....

Role Overview: You will be working as a full-time Associate Consultant - Plastic & Reconstructive Surgery at Max Healthcare in Delhi, India. Your main responsibility will be to provide top-notch patient care within the field of plastic and reconstructive surgery. This will involve carrying out surgical procedures, conducting pre-operative and post-operative consultations, following up with patients, and collaborating with various healthcare teams. Additionally, you will be expected to contribute to departmental meetings, engage in research activities, and ensure compliance with medical regulations and protocols. Key Responsibilities: - Perform surgical procedures in the realm of plastic and ...

As a Clinical Research Trainer at CLRI - CliniLaunch Research Institute, located in Bengaluru, Karnataka, you will play a crucial role in designing, developing, and delivering comprehensive training programs to employees, focusing on clinical research principles, data management best practices, and regulatory compliance requirements. Key Responsibilities: - Develop and implement a robust training curriculum aligned with industry standards and regulatory requirements. - Create engaging training materials, including presentations, handouts, and online learning modules. - Design and deliver customized training programs to meet the specific needs of different teams and individuals. - Conduct eff...

Role Overview: You will be responsible for overseeing and managing the clinical operations of the cardiac rehabilitation program. Your role will involve developing and implementing clinical protocols and guidelines, ensuring high-quality patient care, and leading a multidisciplinary team of health professionals. You will also be required to conduct performance reviews, supervise patient assessments, and drive patient engagement to enhance efficacy. Key Responsibilities: - Oversee and manage clinical operations of the cardiac rehabilitation program. - Develop and implement clinical protocols and guidelines in line with best practices. - Ensure high-quality patient care and adherence to clinic...