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Clinical Trial Project ManagerRef: mc22680

Salary:€45000 - €50000 per annum

Added:13 Feb 2018

Region: Europe

Sector: Pharmaceutical

Sub Sector: Clinical Research

Clinical Trials Project Manager As an experienced Clinical Trials Project Manager in the Scientific Operations Department our clients Headquarters (HQ), you will focus on the set-up and execution of international clinical studies (Phase II / III) or related research projects with a variety of partners. You will be based in Brussels, Belgium, report to a Project Management Leader (line manager) and the Scientific Director, and will be engaged in the following types of activities: *Serve as a main study contact between multiple partners, including member groups, pharmaceutical industry partners, and a variety of vendors for specific clinical trials *Coordinate HQ responsibilities for individual clinical trials, e.g., - conduct of group surveys / site feasibility - set up of study governance committees and related documentation - coordination of governance committees and working groups and their meetings (including taking minutes) - development of study contracts and budgets in collaboration with the Legal and Finance departments, - prepare, manage and follow-up on meetings between partners (including taking minutes) - Prepare and/or review study documents and communications - Assist in preparing reports and articles if needed - Assist in preparation and follow-up of study-related grants if needed - other scientific operations activities as needed - ensure that principles and processes are adhered to, under the guidance of Project Management Leaders *Organise internal team meetings *Maintain HQ study / project files *Assist Project Management Leaders as needed *As part of a project management team, contribute to the improvement of all processes and procedures as well as all related documentation in HQ QUALIFICATIONS SOUGHT: *Academic degree, preferably in a (para)medical discipline *Experience in the set-up and management of all operational aspects of clinical trials (in academia, industry, or CRO) *In-depth knowledge of methodologies, regulations and procedures related to clinical trials *Experience in oncology clinical trials a plus *Possess strong analytical skills and highly organized project management abilities, keeping an eye on both detail, while maintaining a broad overview *Ability to: - work effectively in multicultural teams within headquarters and the 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 *Native or native-like written and spoken English; French, Dutch or other languages a plus *A high level of integrity and sense of responsibility and professionalism

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