Clinical Research Coordinator

1 week ago

Bengaluru, Karnataka, India beBeeClinical Full time ₹ 1,04,000 - ₹ 1,30,878
About the Role

As a key member of our team, you will be responsible for managing participant interactions and sample collections. Your primary focus will be on ensuring the success of clinical trials through effective recruitment, informed consent processes, and regular follow-ups.

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  • Develop and implement strategies for participant recruitment, adhering to study protocols and safety procedures.

You will also be responsible for conducting field visits, collecting biological samples, and maintaining accurate records of all participant interactions and sample collections.

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  • Conduct field visits for community-based or site-based recruitment and collect biological samples such as swabs, blood, etc., adhering to study-specific protocols and safety procedures.

In addition, you will assist senior team members with coordination of clinical trial activities, including scheduling and conducting monitoring visits.

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  • Assist senior team members with coordination of clinical trial activities, including scheduling and conducting monitoring visits.

Your role will also involve training site personnel on Good Clinical Practice (GCP) and protocol adherence.

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  • Train site personnel on GCP and protocol adherence.

Furthermore, you will maintain accurate records of all participant interactions and sample collections, and support the team with any other study-related tasks as needed.

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  • Maintain accurate records of all participant interactions and sample collections; support the team with any other study-related tasks as needed.

We are looking for a highly motivated and detail-oriented individual who can effectively manage multiple tasks and prioritize responsibilities.

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  • Work collaboratively with cross-functional teams to achieve study objectives.

This is an excellent opportunity for someone who is passionate about clinical research and wants to contribute to the advancement of medical knowledge.

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