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Job Details

Biometrics Project Manager

Company: Chiltern
Location: Office based in any of our European offices or home based anywhere in Europe
Reference: PL-2018-21310
Closing Date: 18 Aug 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

Covance is seeking a Biometrics Manager to work within our Clinical Data, Analysis, and Reporting Organization department. In this role you will coordinate Data Management, Programming, and Statistics projects, teams, and deadlines and be responsible for client relationship management. If you are an experienced Project Manager within clinical research then we would love to hear from you.

Requirements:

Job Background

  • Biometrics Project Manager required to work for Covance
  • You will be employed by Covance and work within our Clinical Data, Analysis, and Reporting Organization department.
  • Coordination of Data Management, Programming, and Statistics projects, teams, and deadlines and be responsible for client relationship management
  • Office based in in any of our European offices or home based anywhere in Europe

Covance is seeking a Biometrics Manager to work within our Clinical Data, Analysis, and Reporting Organization department.  In this role you will coordinate Data Management, Programming, and Statistics projects, teams, and deadlines and be responsible for client relationship management.  This is a permanent, full-time role.  If you are an experienced Project Manager within clinical research then we would love to hear from you.  This is an incredibly exciting time to be joining Covance as we continue to grow and expand.

 

Job Primary Functions

  • Has overall responsibility for assuring timeliness and quality of work for studies
  • Ensure that the highest levels of client service are maintained
  • Identify specific Project Integration requirements from clients
  • Coordinate Data Management, Programming, and Statistics projects, teams, and deadlines
  • Communicate on a regular basis with assigned clients regarding questions, concerns, and project status
  • Organize, chair, and record minutes for all cross-functional Project Integration project meetings
  • Facilitate meetings with Sponsors
  • Ensure the relevant personnel are kept informed of problems that may affect the project performance
  • Coordinate receipt, inventory, accountability, and disposal of study related information
  • Ensure all appropriate documentation and procedures are performed upon project completion
  • Update the Project Integration internal timelines for allocated projects in a timely manner. Renegotiate timelines as appropriate
  • Ensure mechanisms in place to maintain flow of appropriate information between disciplines on project team
  • Provide senior management with estimates of group capacity and needs and updates on timelines and projects
  • Keep senior management and/or client services informed of pertinent project or client related information (i.e., work scope changes)
  • Assist Director of Project Integration in preparing proposals and attend client meetings as needed
  • Assist QA and Client Services with client visits and interactions as appropriate
  • Develop new business by building successful client relationships
  • Liaise with Quality Assurance regarding regulatory compliance of study conduct and Sponsor audits
  • Write and update SOPs as required
  • Lead review and amendment of departmental processes and supporting documentation
  • Motivate others to complete high quality work efficiently

 

A comprehensive full job description is available.

 

Job Qualifications

  • BS or BSc in Science, Medical, or related field
  • Knowledge/experience with drug development
  • Knowledge/experience clinical research preferred
  • Minimum of 5 years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
  • In lieu of the above requirements, candidates with >5 years supervisory experience in a health care setting and 4 years clinical research experience in the pharmaceutical or CRO industries will be considered
  • Competent user of MS Excel, MS PowerPoint, MS Project
  • Financially savvy
  • Excellent communicator with strong negotiation skills
  • You must be fluent in English language (both verbal and written)

 

MORE INFORMATION AVAILABLE ON REQUEST

For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 1753 216 727.  To apply, please send your CV to peter.lewis@covance.com - peter.lewis@covance.com

 

About Covance:

As the drug development business of LabCorp and the world’s most comprehensive drug development service company, we have helped pharmaceutical and biotech companies develop 100% of the top 50 prescription drugs in the marketplace today.  Because of our broad experience and specialized expertise, we’re in a unique position to supply insights that go above and beyond testing.  Together with our clients, we create solutions that transform potential into reality.  For more information on Covance please visit: www.covance.com. 

 

Keywords:

Manager, Project Integration, Biometrics Project Manager, Project Data Lead, Data Services Project Manager, Data Team Lead, Data Manager, Data Management, Statistical Programming Manager, Statistical Programmer Manager, Project Manager, Project Management, Chiltern, Covance, clinical research, contract research organisation, CRO, pharma, pharmaceutical, MS Project, Microsoft Project



Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.

Salary

on application

Position Type

Permanent
Full Time

Contact

Email Peter Lewis - Peter.Lewis@chiltern.com
+44 (0) 1753 216 727

Apply for this job: Biometrics Project Manager

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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