Apply for this job

For more information speak to Mark Cussens on 00 44 1727 817 623

To apply by email markc.50526.5174@keypeople.aplitrak.com

Apply Now

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

Apply Now Back To Jobs

We can support your employee requirements

Speak with our support team on 01727 811 634

Contact Us