Clinical Trial Associate

Proclinical are recruiting for a Clinical Trial Associate, on behalf of a mid-sized MedTech organisation based in Basel, Switzerland. This is a full-time, 12-month contract role with option to go permanent, offering hybrid / remote working.

Overview:

Our partner develop truly innovative drug-eluting devices for the treatment of complex cardiovascular conditions and have been partnering some some key players in the Cardiovascular arena. Their lead product is currently undergoing trials in the US, while it has obtained approval across Europe, APAC and LATAM.

Key Responsibilities:

• Provide assistance for the implementation of worldwide clinical trials, from the initiation phase to the finalization.
• Guarantee administrative support for clinical research groups, including documenting meeting discussions and tracking task follow-ups.
• Establish, handle, and monitor the Trial Master File (TMF) in accordance with ICH GCP guidelines, and aid in examining and inspecting vendor TMF for adherence to regulations.
• Contribute to the development of departmental standard operating procedures (SOPs) and processes.
• Participate actively in both internal and external clinical study groups.
• Ensure prompt payment processing of trial invoices, maintain financial records for each study, and track invoice records.

Experience:

• Bachelor degree in Science or equivalent degree.
• At least 3 years of experience in clinical trial support in the pharmaceutical industry.
• Good understanding of the drug development process.
• Familiar with clinical trial documentation and regulatory requirements.

If you are having difficulty in applying or if you have any questions, please contact Roy Nelson at +44 203 148 8373.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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