Clinical Trial Manager (remote based)

Hobson Prior is currently looking for a Clinical Trial Manager for an exciting permanent opportunity at a leading pharmaceutical organisation, based in Belgium, working remotely.

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

Key Responsibilities:

• Coordinate with Trial Team to ensure CAPAs are resolved timely. Act as CAPA owner or contributor, as appropriate.
• Guide the Study Management Team including providing updates to all trial team members on deliverable status.
• Ensure availability of required reports to support real time tracking of trial status according to trial plan.
• Manage timely and accurate documentation and communication of trial progress.
• Ensure that the Study Management Team (SMT) operates in a constant state of inspection readiness.
• Act as primary contact for Country and Regional staff.
• Act as the primary contact person for the local teams within GCDO.
• Partner with the Global Trial Lead to execute and oversee central activities from planning, trial start up, through the life of trial to close-out.
• Ensure issue escalation and drive issue resolution.
• Services rendered will adhere to applicable SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.
• Any other assigned duties.

Key Skills:

• Excellent leadership skills and ability to manage multiple stakeholders.
• Strong project planning/management.
• Proven ability to promote team productivity and cohesiveness.
• Independent complex decision making.
• Excellent verbal and written communication skills leading to successful team collaboration.
• Strong analytical skills, and simultaneously demonstrates the ability to manage ambiguity when limited information is available.

Requirements:

• BS degree or equivalent, in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• A minimum of 6 years clinical trial management experience in the pharmaceutical industry or CRO. Specific therapeutic area experience.
• Strong working knowledge of ICH-GCP, local laws and regulations.
• Ability to understand and competently plan and have oversight of country and select vendor budgeting processes, i.e. Understand and be aware of country Out of Pockets (OOPs) and FTE cost drivers.
• Superior clinical research operational knowledge. Proven track record in successfully managing various aspects of trials from start-up to database lock and trial closure.
• Demonstrated effective leadership to proactively drive the Study Management Team through key stages of trials, as well as delegation skills.
• Experience and ability in coordinating global teams in a virtual environment for a minimum of 2, preferably 3 years.
• Experience in developing presentations and presenting key information to stakeholders.
• Strong IT skills, including knowledge of standard Microsoft applications, Trial Master File, Clinical Trial Management System, and willingness to learn new systems.
• Proficient in speaking and writing local country language and English.
• The ability to travel.

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.