TrialCraft Clinical Research Services Pvt. Ltd. provides versatile solutions in the clinical research sector. With a focus on high-quality clinical trials and research services, TrialCraft supports various stages of clinical studies, ensuring they meet international standards and regulatory compliance.
Job Description: Clinical Research Coordinator (CRC)
As a Clinical Research Coordinator (CRC) at TrialCraft, you will play a crucial role in supporting clinical research projects. The position is open to freshers and candidates with up to 1 year of experience, offering an excellent opportunity to start a career in the clinical research field.
Key Responsibilities:
- Assist in managing clinical trials and ensure compliance with protocols.
- Maintain accurate study records and documentation.
- Ensure that all study procedures adhere to ICH-GCP (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use – Good Clinical Practice) guidelines.
- Coordinate between different departments, investigators, and study participants.
- Monitor study progress and report any issues to the study team.
Qualifications:
- Education: Life science graduates are eligible to apply (e.g., B.Sc. in Life Sciences, Biotech, Microbiology, or related fields).
- Experience: 0 to 1 year of experience as a CRC or in a related field (freshers are welcome).
Skills:
- Good Communication Skills: Ability to communicate effectively with team members and study participants.
- Knowledge of ICH-GCP: Understanding of the international guidelines for clinical trials.
- Quick Learning Skills: Ability to grasp new concepts quickly and efficiently.
How to Apply:
To apply, send your CV to trialcraftpharma@gmail.com.
