Clinical Research Associate

Airvin Skills; Chennai District, Bengaluru, Hyderabad; On-site; INR 167,400 - 279,000; Part time

Job summary

Airvin Skills is seeking a Clinical Research Associate (CRA) intern in Chennai to assist in managing clinical trials and studies. The ideal candidate will collaborate with research teams, ensuring compliance and data accuracy, while gaining hands-on experience in the field.

This opportunity is best suited for those currently enrolled in Life Sciences, Pharmacy, or Nursing programs. Strong communication and organizational skills are essential. This role promises immersive learning and substantial involvement in study processes.

Qualifications

• Currently enrolled in a Bachelor's or Master's degree program in a related field.
• Excellent communication and interpersonal skills.
• Detail-oriented with strong organizational and time management abilities.
• Ability to work independently and as part of a team.

Responsibilities

• Assist in protocol development and site selection for clinical trials.
• Support regulatory compliance and assist with documentation.
• Monitor data collection and report adverse events.
• Maintain accurate documentation and engage in learning opportunities.

Skills

Excellent communication and interpersonal skills

Detail-oriented

Strong organizational abilities

Ability to work independently

Education

Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing or related field

Job description

Job Type- Fresher or Internship level Clinical 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 safe.

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.