Clinical Project Associate

Biocrucible

Cambridge, UK

We are seeking a highly motivated and detail-oriented Clinical Project Associate to join our dynamic team. This is a home-based role with some travel to our offices in Cambridge (UK). The ideal candidate will play a crucial role in supporting the clinical project team in various activities to ensure the successful execution of clinical trials and research studies.

Primary Responsibilities Of The Position

Protocol Development:
• Assist in the drafting and review of clinical study protocols.
• Contribute to the development of study-related documents and ensure compliance with regulatory requirements.

Clinical Study Design:
• Provide support in the design and planning of clinical studies.
• Collaborate with cross-functional teams to ensure study objectives are met.

Documentation:
• Maintain accurate and up-to-date documentation for clinical trials.
• Assist in the preparation and submission of regulatory documents.

Research:
• Conduct literature reviews and stay updated on relevant... More Detail

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