Clinical Data Coordinator

1 week ago


Chennai Tamil Nadu, India Vinsys IT Services Pvt Ltd Full time

**Job description**

**Role & responsibilities**:

- Overseeing the collection, validation and processing of clinical trial data.
- Developing and implementing data management procedures for clinical trials.
- Supporting and facilitating the review of medical coding for validity and completeness.
- Ensuring compliance with applicable regulations, protocols and standard operating procedures in India.
- Maintain the highest data quality standards throughout the data lifecycle, from data collection to database lock.
- Stay updated on industry best practices, technological advancements and regulatory requirements related to clinical data management.
- Certification in clinical data management (like CCDM).
- Knowledge of CRF design, MS Project and analytical capabilities.
- Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM).
- Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
- Understanding of data privacy and protection regulations (e.g., GDPR).
- Effective communication and interpersonal skills to collaborate with other teams.

**Job Types**: Full-time, Part-time, Permanent, Fresher

Pay: ₹25,000.00 - ₹33,000.00 per month

Expected hours: 24 per week

**Benefits**:

- Flexible schedule
- Food provided
- Health insurance
- Leave encashment
- Provident Fund

Work Location: In person



  • Poonamallee, Chennai, Tamil Nadu, India Ethos Clinical Research - Panimalar Medical College Hospital & Research Institute Full time

    The Clinical Research Coordinator (CRC) is responsible for managing and overseeing clinical trials and research studies. The CRC ensures compliance with regulatory requirements, study protocols, and institutional guidelines while safeguarding the well-being of study participants. **Key Responsibilities**: 1. Study Coordination 2. Participant Recruitment...


  • Chennai, Tamil Nadu, India LEADS CLINICAL RESEARCH AND BIO SERVICES PVT LTDS Full time ₹ 2,50,000 - ₹ 3,50,000 per year

    Leads Clinical Research and Bio Services Pvt. Ltd is hiring Clinical Research Coordinators in Chennai and Bangalore.Experience: 1 year months to 3yearsQualification: Degree with Life Science background, Diploma in Clinical Research, MSc. Clinical Research, Pharm DCore ResponsibilitiesCoordinate Screening and Consenting process, Source documentationUpdate...


  • Valasaravakkam, Chennai, Tamil Nadu, India H-CURA PVT LTD Full time

    **Job Title**: Clinical & Patient Coordinator (Nursing Profile) **Job Summary**: We are looking for an experienced and compassionate Clinical & Patient Coordinator with a nursing background to streamline patient care, coordinate clinical workflows, and ensure a smooth and efficient experience for patients from admission to discharge. This role bridges the...


  • Chennai, Tamil Nadu, India Cipaca healthcare & services pvt ltd Full time

    **Job Title**: Clinical Cluster Coordinator **Location**: Chennai, ECR **Key Responsibilities**: - Oversee day-to-day administrative operations within clinical departments. - Manage end-to-end manpower recruitment, including hiring and onboarding healthcare professionals. - Conduct quality assessments and implement improvement strategies to enhance...


  • Chennai, Tamil Nadu, India Allucent Full time

    At Allucent TM we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe We are looking for Clinical Data Manager III CDM III to join our A-team As CDM III at Allucent you will manage and coordinate DM deliverables from...


  • Chengalpattu, Chennai, Tamil Nadu, India SRM Institute of Science and Technology Full time

    Job Title: Clinical Research Coordinator Qualification: Pharm.D / M.Pharm/ M.Sc or B.Sc in Life Science Experience: UG with 3+ Years / PG - Fresher or 1 Year Responsibility: Coordinate clinical trials, patient management, and regulatory compliance. Increased capacity for managing trials with improved efficiency and compliance. Interview on 18/03/2025 at...


  • Chennai, Tamil Nadu, India SMOConnect Clinical Research Services Pvt Ltd Full time

    Maintaining the source documents, CRF's, Investigator Site File and other study related documents according to ICH-GCP guideline - Completing the eCRF - Maintenance of Investigational Product according to the specific temperature. Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits. - Organizing ethics...


  • Chennai, Tamil Nadu, India Icon Full time

    Clinical Data Science Programmer- Office based- Chennai Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization We re proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical...


  • Chennai, Tamil Nadu, India Clinilaunch Research Institute Full time

    Responsibilities: - Develop and deliver training on Clinical Research, Clinical Data Management (CDM), Pharmacovigilance (PV), and Good Clinical Practice (GCP), with additional knowledge of Medical Writing (MW) and Regulatory Affairs (RA) as a plus. - Conduct assessments and provide feedback to improve trainees’ clinical research skills. - Stay updated on...


  • Chennai, Tamil Nadu, India ICON Plc Full time

    Clinical Data Science Associate - Chennai - Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development What You Will Be Doing: - Conducting...