We are looking for a motivated Clinical Research Associate (CRA) to support clinical trial activities and ensure studies are conducted according to protocols, regulatory requirements, and quality standards.
Key Responsibilities
- Support clinical trial activities and study documentation.
- Assist in site coordination and communication with investigators and study teams.
- Maintain Trial Master File (TMF) and essential study documents.
- Support monitoring visits and follow up on site-related activities.
- Review and track study data, reports, and documentation.
- Ensure compliance with study protocols, GCP, SOPs, and applicable regulations.
- Assist with identifying and resolving study-related issues.
- Prepare and maintain study reports and trackers.
- Coordinate with cross-functional teams to ensure timely completion of study activities.
Requirements
- Bachelor's/Master's degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Nursing, or a related field.
- Freshers are encouraged to apply.
- Basic knowledge of Clinical Research, GCP, and clinical trial processes.
- Good communication and documentation skills.
- Strong attention to detail and willingness to learn.
- Good organizational and time-management skills.
- Basic knowledge of MS Office/Google Workspace.
📌 Clinical Reserach Associate (India)
🏢 Clinogenesis Research Institute
📍 India
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.