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Job Details

Protocol Manager

Company: inVentiv Health Clinical
Location: Braine L'Alleud, Belgium
Reference: IH/6167
Closing Date: 17 Dec 17
Type: Full Time
Salary (£): On Application

Job Summary:

Are you ready to work alongside the brightest minds at INC Research/inVentiv Health?


Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose:  shortening the distance from lab to life.  You’ll work alongside the brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most.  In fact, in a recent five-year period, INC Research/inVentiv Health has helped to develop or commercialize at least 82% of novel new drugs approved by the FDA and at least 70% of products granted marketing authorization by the EMA.


For our client, a global pharmaceutical organization we are currently looking for a Protocol Manager and/or Associate Protocol Manager. In this role you will be working from the Client’s office in Braine L’Alleud but you are allowed to work from home 1 day per week once you are fully trained.  


A Protocol Manager will manage tasks within all phases (start up, enrollment, maintenance, and close-out) of clinical research studies, primarily focused on Phase 2b and 3 studies. They will develop expertise in assigned therapeutic and disease areas.


An Associate Protocol Managers will be assigned at the protocol or program level to complete specific tasks within the protocol or program under the guidance and support of a Protocol Manager (eg, data listing review, vendor contracting and oversight, etc). In some cases, the Associate Protocol Manager may be assigned to independently oversee a protocol (eg, strategic oversight of the study including risk and issue identification and planning, matrix management of assigned study team members, global project management, etc). The Associate Protocol Manager will act as a matrix leader for the global clinical operations team and is accountable for the timely execution of tasks they are assigned within protocols or programs.



The ideal candidate has:

  • At least a minimum of 4 years of experience in the pharmaceutical or related industries.
  • Minimum education BA/BS.
  • Demonstrates the ability to drive clinical trial activities: i.e. experience in aspects of clinical trial management including study start-up, enrollment, maintenance, closeout, regulatory obligations, vendor oversight, data listing review, adverse event reporting, and budget management.
  • Demonstrates project management skills including project planning and prioritization, timeline management, time and meeting management skills, and ability to identify and appropriately manage or escalate risks.
  • Ability to form positive working relationships with team members and stakeholders through effective communication, collaboration, and expectation setting.
  • Understanding of ICH/GCP Guidelines and local regulatory guidelines or regulations; knowledge of clinical trial conduct; knowledge of the pharmaceutical industry and of the pre-clinical, clinical, regulatory and commercial components.
  • Effective oral, written and interpersonal communication skills.
  • Experience with conflict and issue management.
  • Ability to learn new technology and effectively use Clinical Trial Management Systems (CTMS) and other technology platforms.
  • Demonstrated ability to multi-task and manage high performance demands.



How to apply?

Are you ready to work alongside the brightest minds at INC Research/inVentiv Health? In this role you’ll be fully employed by INC Research/inVentiv Health and will enjoy our very competitive primary and secondary benefits. Please contact Eveline Wigtman or Irene Houtsma via and refer to job number 6167.

Apply for this job: Protocol Manager

Contact Information:

Address:  France
41 rue des trois Fontanot
92 000 Nanterre

Reasons to work for inVentiv Health Clinical
Website:  Visit Our Web Site

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