We are looking for a Clinical Research Associate to support clinical trial activities and ensure studies are conducted in compliance with applicable protocols, SOPs, and regulatory requirements.
Key Responsibilities:
- Support site selection, initiation, monitoring, and close-out activities.
- Conduct site visits and maintain study documentation.
- Review source documents, CRFs/eCRFs, and essential trial records.
- Coordinate with investigators, study teams, and vendors.
- Track protocol compliance, deviations, and study timelines.
- Ensure adherence to GCP, SOPs, and regulatory requirements.
- Prepare monitoring reports and maintain Trial Master File (TMF) documentation.
Skills Required:
- Knowledge of Clinical Research, ICH-GCP, and clinical trial processes.
- Good communication and documentation skills.
- Solid attention to detail and coordination abilities.
- Basic knowledge of MS Office and clinical trial systems.
Education: B.Pharm / M.Pharm / Pharm.D / Any Life Sciences Graduate & Post Graduate / Biotechnology / Clinical Research or related field.
📌 Clinical Research Associate-Freshers Only (Bengaluru)
🏢 Proxima Skills Training Consulting Services
📍 Bengaluru
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