Head of Clinical Trials

☞ PharmiWeb.jobs: Global Life Science Jobs

見る: 145

更新日: 08-12-2025

場所: Charleroi Hainaut

カテゴリー: その他の

業界: Staffing Recruiting

レベル: Director

ジョブタイプ: Contract

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仕事内容

Hobson Prior are currently seeking for a Head of Clinical Trials to join a fantastic pharmaceutical organisation on a contract basis located in Gosselies. Our client is focused on producing ground-breaking remedies for cancer.Please note that to be considered for this role you must have the right to work in this location.Key Responsibilities
  • For this position, you will supervise and handle CROs, vendors, and internal personnel to guarantee successful performance of the clinical trial which involves serving as the main point of contact for problem escalation and resolution.
  • Partake in both individual and team development via training initiative, team building actions and training of junior personnel.
  • You will serve as a cross-functional liaison between both the clinical operations and development teams and assure efficient alignment concerning plans, needs and deliverables.
  • Form performance indicators and implementation to guarantee the successful implementation of clinical trials to agreed timelines.
  • The ideal candidate will serve as a representative in all facets of trial operations and offer updated as needed to senior management, project teams and any other crucial internal shareholders.
  • Work alongside the strategic sourcing head to guarantee suitable deployment of vendors, oversight, governance, and issue escalation.
  • Any other assigned duties.
Key Skills
  • Able to present self with a high level of integrity and in a professional manner when serving as a representative.
  • Works well independently with a drive to succeed.
  • Capable of handling and prioritising various tasks simultaneously while working within a fast-paced setting.
  • Communication skills both verbally and in writing.
  • Works well in a team, as well as cross-functionally.
Requirements
  • Educated to a degree level in a scientific field, ideally a Master’s.
  • Ability to handle clinical operations actions and personnel.
  • At least 12+ years of experience in guiding various international cross-functional clinical studies such as phases I-II, ideally also phase III, as well as vendors.
  • Familiarity with oncology.
  • Comprehension of and familiarity within the drug development procedure which involves clinical study management, drug safety surveillance and reporting needs, international regulatory reporting needs, clinical study report needs, etc.
  • Expertise of ICH/GCP, ISO-14155, FDA, MDR, and EU guidelines when suitable.
  • Demonstrated ability in managing, motivating and engaging with clinical personnel.
  • Know-how of the principles of project management and planning.
  • Capable of distilling multifaceted information from various sources and draw meaningful conclusions and acumens, as well as discuss and display those concerns for senior management.
  • Computer literacy in MS Office applications.
  • Willing to travel for business needs up to 20% of the time.
Apply NowIf you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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締切: 22-01-2026

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