Posted:2 weeks ago|
Platform:
On-site
Full Time
We are seeking a highly organized and detail-oriented Clinical Trial Assistant (CTA) to support our clinical
research team. The successful candidate will assist in the coordination of clinical trials, ensuring
compliance with Good Clinical Practice (GCP), regulatory requirements, and study protocols.
1. Assist in the preparation and maintenance of study documents, including informed consent forms,
case report forms, and study logs.
2. Coordinate with study sites to ensure smooth study execution.
3. Assist in patient recruitment, screening, and enrollment.
4. Manage study supplies, lab samples, and other study-related materials.
5. Perform data entry, data management.
6. Assist in the preparation of regulatory submissions, progress reports, and study closure documents.
7. Maintain study files, both physical and electronic.
8. Communicate with study teams, Investigator and sites.
1. Bachelor's degree in Life Sciences, B. Pharma M. Pharma.
2. 6 months -2 years of experience in clinical research.
3. Knowledge of GCP, ICH guidelines, and regulatory requirements.
4. Excellent organizational, communication, and interpersonal skills.
5. Ability to work independently and as part of a team.
6. Proficiency in Microsoft Office & Excel and clinical trial management systems.
1. Certification and Experience in clinical research.
2. Experience with electronic data capture (EDC) systems.
3. Knowledge of clinical trial regulations and guidelines.
If you're passionate about clinical research and have a keen eye for detail, we'd love to hear from you!
Apply with your resume and cover letter.
Meril
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