Job Type- Fresher or Internship levelClinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are protected.Responsibilities:1. Assist in Protocol Development:

- Collaborate with the clinical research team to contribute to the development and review of clinical trial protocols.

2. Site Identification and Selection:

- Participate in the process of identifying and selecting clinical trial sites by conducting feasibility assessments.

3. Regulatory Compliance:

- Support the team in ensuring regulatory compliance throughout the clinical trial process.
- Assist in the preparation and submission of regulatory documents to appropriate health authorities.

4. Site Initiation:

- Assist in the initiation of clinical trial sites by coordinating site training activities and ensuring that all necessary documentation is in place.

5. Monitoring and Data Collection:

- Work closely with clinical research associates and investigators to monitor and collect data during the clinical trial.
- Assist in ensuring data accuracy, completeness, and adherence to protocol.

6. Adverse Event Reporting:

- Contribute to the process of monitoring and reporting adverse events,



ensuring compliance with regulatory requirements.

7. Study Close-Out:

- Participate in the close-out activities of clinical trials, including the collection of essential documents and finalizing study reports.

8. Collaboration and Communication:

- Work collaboratively with cross-functional teams, including clinical operations, data management, and regulatory affairs.
- Communicate effectively with investigators, site staff, and study sponsors.

9. Documentation and Record Keeping:

- Maintain accurate and up-to-date documentation of all activities performed during the internship.
- Contribute to the development and organization of the trial master file.

10. Learning and Development:

- Actively engage in learning opportunities provided during the internship to enhance knowledge of clinical research processes and industry regulations.

Qualifications:

- Currently enrolled in a Bachelor's or Master's degree program in a related field (e.g., Life Sciences, Pharmacy, Nursing, etc.).
- Excellent communication and interpersonal skills.
- Detail-oriented with strong organizational and time management abilities.
- Ability to work independently and as part of a team.Role & responsibilities

Preferred candidate profile

📌 Clinical Research Associate (Telangana)
🏢 Airvin Skills
📍 Telangana