Clinical Trial Manager (EU studies), Bucks (UK)

Recruiter
DOCS Global
Location
Marlow
Posted
16 Mar 2019
Closes
31 Mar 2019
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Job Summary Don't miss out on these highly sought-after position, for more details on the various clinical opportunities we currently have, please contact Elisabeth.knighton@docsglobal.com *Applicants who have not had a response within two weeks should assume their application has been unsuccessful. Roles & Responsibilities of the position DOCS is hiring clinical trial managers with commercial clinical study management experience. The Clinical Trial Manager will be responsible for leading the EU/regional matrix team (CRAs, CTAs, etc.) to ensure delivery of country and site level study activities in alignment with the global study project plan. Key Responsibilities include: • Identifying and resolving issues at a regional level • Collaborating with Global PM to ensure country level study delivery is aligned with the global study project plan • Contributing to study-level risk assessments • Leading and continually review regional risk mitigation activities to ensure study delivery to plan • Overseeing regional insourcing /outsourcing partner deliverables to the required standards • Partnering with multi-disciplinary teams to ensure regional, country and site vendor set-up, conduct and quality • Leading regional documentation and required tool and systems set-up • Contributing to regional aspects of Drug Supply Plan • Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines Job Requirements • BA/BS/BSc or RN • Strong knowledge of clinical development process and procedures • Project planning experience including oversight • Proven track-record of European clinical studies (commercial/industry-sponsored studies) • Ideally 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company. • Experience in oversight of external clinical research vendors (CROs, central labs, imaging vendors, etc.) • Full-time availability • Full and valid UK working eligibility • Start date negotiable Remuneration & other details • Permanent contract of employment • Full-time • Office-based with 2 days home-working flexibility • Office-based either in Marlow (Bucks) or Eastleigh ( Hampshire) • Excellent salary package • Company benefits (25 days annual leave, car allowance, pension, life assurance, and healthcare cover) Send your CV now to find out more to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

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