Job details

Project Manager

Company details

The Breast International Group (BIG) is a non-profit research organization that represents the largest global network of academic groups dedicated to breast research. 30+ clinical trials are run or under development under the BIG umbrella at any one time.

BIG is recruiting:

PROJECT MANAGER

Function

As an experienced Clinical Trials Project Manager in the Research Operations Department at BIG Headquarters (HQ), you will have the oversight of all study activities related to the set-up and coordination of international clinical studies (Phase II / III) or research programs internally, and with external partners. You will be based in Brussels, Belgium, report to a Project Management Leader / Research Operations Director. Main activities are:

  • Serve as main study contact for operational activities for BIG HQ, with multiple partners, including BIG member groups, pharmaceutical industry partners, and a variety of vendors for the clinical trials or research programs.
  • Coordinate BIG HQ responsibilities for individual clinical trials, including, but not limited to:
    • Conduct of group / site feasibility surveys
    • Set up of study governance committees and related documentation
    • Coordination of governance committees and working groups and their meetings (including taking minutes)
    • Development and follow up on study contracts and budgets in collaboration with the BIG HQ Legal and Finance departments
    • Prepare, manage and follow-up on internal and external meetings between partners (including taking minutes)
    • Lead internal and external discussions related to operational activities of assigned studies
    • Prepare and/or review study documents and communications
    • Assist in preparation and follow-up of study related grants if needed
    • Other scientific operations activities as needed
    • Ensure that BIG principles and processes are adhered to, under the guidance of Project Management Leaders/Research Operations Director
  • Maintain BIG HQ study / program files and assist with administrative tasks as needed.
  • Contribute to the improvement of all processes and procedures and all related BIG HQ documentation.

Profile

  • Academic degree, preferably in a (para)medical discipline
  • 3 – 4 years experience in the set-up and management of all operational aspects of clinical trials (in academia, industry, or CRO)
  • A good knowledge of GCP and methodologies, regulations and procedures related to clinical trials
  • Experience in oncology clinical trials is a plus
  • Previous experience in managing budgets and contracts is a plus
  • Strong analytical, organization, planning and communication skills
  • Sense of diplomacy, and attention to details, while maintaining a broad overview
  • Native or native-like written and spoken English; French, Dutch or other languages are a plus
  • A high level of integrity and sense of responsibility and professionalism
  • Ability to:
    • Work effectively in multicultural teams within BIG headquarters and the BIG network, and across organisational boundaries, respecting differences between people from a variety of linguistic and cultural backgrounds
    • Learn, interpret and apply a variety of complex policies and procedures with minimal guidance
    • Accurately and professionally process a high volume of correspondence, documents and other often sensitive and confidential information
    • Maintain a high level of poise and professionalism while coordinating a diverse variety of daily and special project deadlines simultaneously

Offer

  • The opportunity to contribute to innovative, practice-changing cancer research
  • A stimulating international environment
  • Full-time employment and unlimited duration contract
  • A competitive salary and benefits package

  • Placed on:Wed 17 February 2021
  • Location: Brussels

Profile Group


E-mail

Interested?

For more information:
Call EMMA WAITES
at the number: 02 738 02 63 GSM 0475 614967
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