Clinical Trial Leader

£50-58.81 per hour Ltd
02 Aug 2019
01 Sep 2019
Lucy Stendall
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
CK Group is recruiting for a Clinical Trial Leader to join a company in the pharmaceutical industry at their site based in Leeds on a contract basis for 12 months.

The role offers a pay rate of £50-58.81 per hour Ltd.

The Company:
Our client is a multinational medical devices, pharmaceutical and consumer packaged goods manufacturing company who offer the worlds most comprehensive portfolio of orthopaedic and neuro products and services for joint reconstruction, trauma, spine, sports medicine, neuro, cranio-maxillofacial, power tools and biomaterials.

The Location:
The role is based at our client's state of the art R&D and production facility in Leeds. This site is a short distance from the M621 and is easily commutable on public transport as it is a short distance from Leeds city centre.

The Role:
Serve as a Clinical Trial Leader within Clinical & Medical Strategic Operations to execute company sponsored clinical trials for Medical Devices.

Key Responsibilities:
- Manage all operational activities of assigned clinical studies.
- Serves as a member of the clinical trial/study/program core team and may serve as the liaison with the Clinical Franchise and Clinical BSDM for projects under his/her responsibility.
- May serve as the primary contact for clinical trial sites.
- Can independently solve problems arising during clinical study execution, and will seek guidance for more complex problems, as needed.
- Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders.
- May be involved in other tasks to support Clinical & Medical Strategic Operations and Clinical Franchise as needed.
- Track and manage assigned clinical trials/programs budgets to ensure adherence to business plans.
- Support the implementation of new clinical systems/processes, as needed.
- Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel.
- Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance.
- Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency.

Your Background:
- Minimum of a Bachelor's Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.
- BS with at least 6 years, MS with at least 5 years, PhD with at least 3 years of relevant experience preferred.
- Previous experience in clinical trial management is required.
- Experience working well with cross-functional teams is required.
- Clinical/medical background a plus.
- Medical device experience a plus.

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 46203 in all correspondence.

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