Clinical Research Associate Responsibilities:

- Creating and writing trial protocols, and presenting these to the steering committee.
- Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.
- Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
- Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.
- Ordering, tracking, and managing IP and trial materials.
- Overseeing and documenting IP dispensing inventory, and reconciliation.
- Protecting subjects’ confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.
- Conducting regular site visits, coordinating project meetings, and writing visit reports.
- Implementing action plans for sites not meeting expectations.
- Liaising with regulatory authorities.
- Ensuring compliance with SOPs and local regulations,



and ICH and GCP guidelines.
- Other tasks and responsibilities as needed.

Clinical Research Associate Requirements:

- Bachelor’s degree in biological science or a related field.
- Knowledge of the pharmaceutical industry, terminology, and practices.
- Knowledge of FDA regulations and their practical implementation.
- Strong verbal and written communication skills.
- Proficient computer skills.
- Proficient with Microsoft Office Word, Excel, and PowerPoint.
- Ability to manage and prioritize workload effectively.
- Available to travel extensively and on short notice, and ability to manage travel schedules, such as flight schedules.

Job Types: Full time, Permanent, Fresher

Pay: ₹372,572.86 - ₹733,555.00 per year

Benefits:

- Health insurance
- Paid sick time
- Provident Fund

Work Location: In person

📌 Clinical Research Associate (India)
🏢 Refined Reports Data
📍 India