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Job Details

Clinical Project Manager - Multiple Locations

Company: Planet Pharma Staffing Limited
Location: London
Reference: CPM/CQM12
Closing Date: 06 Feb 17
Type: Full Time
Salary (£): Competitive
Benefits: Attractive

Job Summary:

Excellent opportunity for a Clinical Project Manager to join a Global organisation and be involved in studies across the EU.


Clinical Project Manager

Company: Global CRO
Type: Permanent
Location: Multiple - London, Reading, Buckinghamshire
Travel: Nationwide travel required


Excellent opportunity for an experienced Project Manager to join a world leading Global CRO on a permanent basis where you will be involved in a variety of therapy areas and phases of development.

My client is looking for experienced candidates with a minimum of 2 years as a Project Manager and ideally you would have made the natural progression from CTA, CRA and now PM.

This organisation is growing rapidly, and are currently seeking a full-time, office-based Clinical Project Manager to join their Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.


  • Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles and ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
  • Develop study management plans, together with team assignments and accountabilities and oversight of database maintenance.
  • Serve as primary project contact with Sponsor to ensure communication is maintained and reporting schedules are adhered to.
  • Collect information on team performance against contract, customer expectations, and project baselines.
  • Lead problem solving and resolution efforts to include management of risk, contingencies and issues.
  • Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
  • Provide input for the development of proposals for new work and manage project budgets.
  • Prepare and present project information at internal and external meetings.
  • Participate in proposal development and in the bid-defense process with guidance and supervision.
  • Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site/visits and ongoing mentoring of CRA team.


  • Bachelor's degree in life sciences or related field and 5 years' clinical research experience including 2 years' project management experience and experience in clinical operations; or equivalent combination of education, training and experience.
  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines
  • Good therapeutic and protocol knowledge
  • Strong communication and interpersonal skills, including good command of English language
  • Good problem solving skills
  • Demonstrated ability to deliver results to the appropriate quality and timeline metrics
  • Good teamwork skills
  • Excellent customer service skills
  • Good presentation skills
  • Strong software and computer skills, including MS Office applications
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients



Please call Sam Chapple on 0203 868 8607  or email for more information.


Clinical, Pharmaceutical, CRO, Oncology, Respiratory, Cardiovascular, Neurology, Diabetes, Infectious disease, London, Middlesex, Surrey, Buckinghamshire, Hertfordshire, Essex, Homebased, Nationwide


Apply for this job: Clinical Project Manager - Multiple Locations

Contact Information:

Address:  Head Office
10 Greycoat Place, London,
Tel:  +44 203 868 1000
Website:  Visit Our Web Site

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