Posted to MedZilla on 4/30/2017


ProClinical

England, Global Clinical Study Manager CR_MP_11567-MZ


 
 

A leading biotech in London are looking for a number of Global Clinical Study Managers to join their ever present and growing clinical operations department. This is a permanent role with flexible working, including 2 days a week working from home. Our client is a world-leading independent biotechnology companiy, with global revenues in excess of $18 billion and over 18,000 employees. 

Role Responsibilities:

  • Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP
  • Oversee the quality and scientific integrity of clinical operations for studies at a global level
  • Collaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables
  • Leading the Clinical Study Team to drive effective decision making.
  • Planning, management and reporting of clinical studies conducted by Global Development through oversight of cross-functional study activities, identification and resolution of issues, and communication of study timelines/deliverables
  • Ensuring implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines
  • Management of study budget and timelines
  • Management of vendors to the required standards
  • Travel as required to support the execution of clinical studies as required.

Job Requirements:

  • BA/BS/BSc or RN
  • Regional clinical project management experience
  • Experience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.)
  • Broad experience working in life sciences or medically related field, including general biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company)

Preferred Qualifications:

  • BA/BS/BSc in the sciences or RN
  • Global clinical project management experience
  • Previous management experience of direct reports
  • Extensive clinical research experience working in life sciences or medically related field, including general biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company)
  • Previous management experience of direct reports
  • Advanced knowledge of global clinical project management
  • Knowledge of time, cost and quality metrics, Key performance indicators (KPIs)

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Matthew Pike on +44 207 4400 639 or upload your CV on our website www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.


Please visit our website at www.proclinical.com

 
 


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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.