Job Summary:
We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to manage and coordinate clinical trials, ensuring compliance with regulatory guidelines and protocols. The CRC will work closely with principal investigators, study participants, and regulatory bodies to support successful trial execution.
Key Responsibilities:
- Coordinate all aspects of clinical research trials from initiation to close-out, including patient recruitment, screening, consent, and follow-up.
- Ensure adherence to trial protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Collect, document, and maintain accurate study data, including case report forms (CRFs) and electronic data capture (EDC) systems.
- Communicate with internal and external stakeholders, including sponsors, regulatory authorities, and ethics committees.
- Monitor study progress, report adverse events, and ensure the safety and welfare of study participants.
- Assist in the preparation and submission of regulatory documents, including IRB submissions and informed consent forms.
- Manage trial-related budgets, supplies, and timelines.
- Collaborate with multidisciplinary teams, including physicians, nurses, and laboratory staff, to ensure smooth trial operations.
- Provide education and support to study participants and their families regarding the trial procedures and outcomes.
Qualifications:
- Bachelor's degree in Life Sciences, or a related field (Master's degree preferred).
- Certification as a Clinical Research Coordinator (CRC) or similar is an advantage.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Excellent organizational, time management, and problem-solving skills.
Job Types: Full-time, Permanent, Fresher
Pay: 15,852.01 - 37,459.14 per month
Experience:
- total work: 1 year (Preferred)
Work Location: In person
