Are you an Clinical Research Associate (CRA II/Senior CRA) looking for an exciting opportunity in Bangalore? Navitas Life Sciences is hiring professionals with a strong background in clinical trial monitoring and site management. If you have 4+ years of on-site monitoring experience, this could be your next career move!
Job Description: Clinical Research Associate (CRA II/Senior CRA)
Key Responsibilities:
- Conduct on-site and remote monitoring of clinical trials to ensure compliance with protocols, GCP, and regulatory requirements.
- Perform site selection, initiation, monitoring, and close-out visits.
- Verify source data, case report forms (CRFs), and essential documents for accuracy.
- Ensure site compliance with study protocols, SOPs, and regulatory guidelines (ICH-GCP).
- Identify and resolve site-related issues and ensure timely query resolution.
- Collaborate with investigators, study coordinators, and clinical teams to ensure smooth trial execution.
- Prepare and submit monitoring reports and follow-up letters post-visit.
Qualifications & Skills:
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, or related field.
- 4+ years of experience as a CRA with hands-on on-site monitoring experience.
- Strong knowledge of ICH-GCP, clinical trial protocols, and regulatory requirements.
- Excellent communication, organizational, and problem-solving skills.
- Willingness to travel to investigative sites as required.
About Navitas Life Sciences
Navitas Life Sciences is a leading clinical research and regulatory services provider, supporting pharmaceutical, biotech, and medical device companies. With a focus on patient-centric clinical trials, Navitas offers end-to-end solutions in clinical operations, data management, and regulatory compliance.
How to Apply?
Interested candidates can share their updated CV to recruitment.bangalore@navitaslifesciences.com or connect for more details.
