01Responsibilities
- Assist in the planning and execution of clinical research studies.
- Monitor clinical sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Support data collection, verification, and quality assurance activities.
- Collaborate with investigators and site personnel to ensure accurate and timely data entry and documentation.
- Prepare and review study documents, including informed consent forms and regulatory submissions.
- Participate in study meetings, training sessions, and site initiation visits.
- Maintain accurate records of study-related activities and communicate any findings or issues to the research team.
- Help ensure patient safety and integrity of data by following strict ethical guidelines.
Eligibility Criteria:
- Education: Bachelors degree in Life Sciences, Pharmacy, Biotechnology, or a related field (e.g., B. Pharma, B.Sc. in Biotechnology, or related discipline).
- Experience: Freshers are welcome to apply. Prior internships or exposure to clinical research is a plus.
- Skills:
- Robust organizational and time management skills.
- Excellent attention to detail and ability to follow protocols strictly.
- Strong written and verbal communication skills.
- Proficient in MS Office (Word, Excel, PowerPoint).
- Knowledge of ICH-GCP guidelines is a plus.
Job Types: Full-time, Permanent, Fresher
Compensation: 18,000.00 - 25,000.00 per month
Benefits:
- Cell phone reimbursement
- Commuter assistance
- Flexible schedule
- Health insurance
- Internet reimbursement .
