Clinical Research Leader – Belgium

Excelya>Full-time>Clinical Research Leader – Belgium

Job description

For one of our clients, we are looking for a Clinical Research Leader

Our client is active in medical devices and is located in Brussels. 

This Clinical Research Leader will be responsible for leading and supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization. 

Reports to: 

Clinical Research Manager 

Key Accountabilities and Responsibilities: 

  • Working with limited supervision, independent decision-making; 
  • Execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones;
  • Oversight/Execution of feasibility, selection, set-up, conduct and closure of a clinical trial within the allocated countries; 
  • May provide on-site procedural protocol compliance and data collection; 
  • May serve as the primary contact for clinical trial sites;
  • Track and manage assigned project budgets;
  • Develop clinical trial documents with minimal supervision;
  • Ensure applicable trial registration from study initation through posting of results and support publications as needed;
  • Management/oversight of ordering, tracking and accountability of investigational products and trial materials;
  • Interface and collaborate with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
  • Responsible for delivery of assigned clinical projects, through effective partnership with the study core team, leading to delivery of clinical project commitments;
  • Oversee the development and execution of investigator agreements and trial payments;
  • Responsible for clinical data review; 
  • May perform monitoring activities upon need. 

 

Qualifications and Skills: 

  • Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required;
  • Bachelor with at least 6 years, Master with at least 5 years, PhD with at least 3 years of relevant experience preferred;
  • Previous experience in clinical research or equivalent is required;
  • Experience working well with cross-functional teams is required;
  • Relevant industry certifications preferred; 
  • Clinical/medical background a plus;
  • Experience managing projects a plus;
  • Medical device experience preferred;
  • Fluent in English – working language. 

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