Hobson Prior are currently looking for a Clinical Assessment Manager to join a brilliant pharmaceutical establishment on a contract basis located in Germany. Our client is focused on distributing life-changing resolutions that inspire advancement, foster amenability, and maximise effectiveness for those who conduct clinical trials.

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

Key Responsibilities:

• To guarantee site readiness for clinical assessment activations rendering to the project specific deadlines, for this role, you will supervise the onboarding of new clinical sites.
• To warrant and protect data integrity, you will oversee question notifications and solution procedure with sites.
• Evolve workflow processes for study team based on specific project and study guidelines.
• Act as a main point of contact for clients, examiners/sites by exchanging with them in an optimistic, professional fashion.
• Prepare and uphold adherence to FDA and regulatory guidelines in all features of performing clinical trials.
• To certify deliverables are met in a quality and effective fashion, the ideal candidate will alleviate risk associated with clinical assessments as defined in the project specific scope of work.
• Manage onboarding sites with project start up, which involves testing equipment, mock assessments, and closeout actions linked to clinical appraisals.
• To assist with custom document production for supervising and trailing data captured in the clinical eCOA system.
• Progress project specific mentoring resources for sites as well as internal clinicians in aggregation with the company's MA-PP subject matter experts
• Offer input to encouraging team spirit and productivity by forming communication lines in the project team.
• Presence and promptness are vital for this position.
• Any other assigned duties.

Key Skills:

• Communication skills with the ability to work efficiently in a varied, professional team environment.
• Organised individual with the ability to prioritise workload and manage time accordingly.
• A high attention to detail with the capacity to be confident, flexible and adapt to alterations as well as be people-focused.

Requirements:

• Educated to a degree level in healthcare, life sciences or a similar discipline with pertinent involvement within a pharmaceutical or biotechnology organisation with CNS clinical trials experience which is not essential but beneficial for the role.
• A t least 5 years of experience with research or clinical know-how.
• Capable of reading, comprehending and adjusting guidelines detailed needs and/or to ask suitable queries are required to attain knowledge and comprehension.
• Familiarity with research design, patient care customs, GCPs, FDA guidelines and an exhaustive know-how of medical vocabulary.
• Previous involvement with an eCOA platform is advantageous to the role, but not necessary.
• Computer literacy in common office applications such as Microsoft Office, teleconferencing etc.

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.