CK Group are recruiting for a Clinical Pharmacology Study Manager to join a company in the healthcare industry at their site based in Weybridge on a contract basis for 12 months.
Daily £759.70 per day UMBRELLA
Clinical Pharmacology Study Manager Role:
? Responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials.
? Provide appropriate clinical pharmacology contributions or author the clinical development plan.
? Prepare/review/contribute to clinical study protocols.
? Supervise study setup (in co-operation with Clinical Operations and other study team members review of Task orders and deliverables) and study execution (Kick-off meeting; Site Initiation Visit; regular team meetings; risk management process; issues escalation; management of protocol deviations and blind data review).
? Review/contribute to key study documents e.g. ICF, Statistical Analysis Plan; Analytical Method plan & validations and Bioanalytical documentation.
? Life Science Degree- PhD/PharmD highly preferred with advanced studies in clinical pharmacology and pharmacokinetics.
? Minimum of 8 years experience in pharmacokinetics.
? Solid understanding of clinical drug development.
? Proven ability to effectively liaise and influence internally and externally.
Our client is a global healthcare company, taking on some of the world\'s biggest healthcare challenges.
This Clinical Pharmacology Study Manager role will be based at our clients site in Weybridge, Surrey.
Entitlement to work in the UK is essential. Please quote reference 51800.
Please note that the successful applicant will be required to engage via an FCSA-accredited and CK-approved umbrella company and the rate of pay indicated is an umbrella rate.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Contact: Julie Marshall
- Phone: 01438 723 500
- Reference: 51800
Website: CK Group
- Posted: 30th September 2021
- Expires: 28th October 2021