Clinical Trial Associate (hybrid)

Hobson Prior are looking for a Clinical Trial Associate to join a fantastic pharmaceutical organisation on a permanent basis located in Hampshire with hybrid working available. Our client is focused on drug finding and developing solutions for respiratory illnesses.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this position, you will handle trial supplies, which involves mediating with vendors, and setting up accounts when needed.
• Responsible for tracking, delivering and filing clinical trials documents in a timely manner.
• You will notify the CRA or PM of any discrepancies and problems noted when suitable.
• The ideal candidate will prepare and send of materials to investigator sites.
• Support the set up and upkeep of electronic trial master file and investigator site files.
• Assist with preparing and attending both internal and external study meetings, which involves taking and distributing minutes and action items as well as coordinate investigator meetings when needed.
• Accountable for assisting the CRAs and visiting sites with them if needed.
• You will prepare necessary clinical trial documents.
• Produce and uphold study contact lists for both study teams and sites.
• Any other assigned duties.

Requirements:

• At least 2 - 3 years of experience in a CTA role.
• Willing to travel to site for business needs up to 2 - 3 days per week, or when necessary.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.