Global Clinical Trial Manager *** Belgium*** Homebasedsed

Employer
Docs Global (Continental Europe)
Location
Belgium
Salary
Competitive
Closing date
23 Sep 2020

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Discipline
Clinical Research, Clinical Trials Manager / Administrator
Hours
Full Time
Contract Type
Permanent
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Responsibilities:
The position is responsible for the global coordination of clinical trial management activities for internally managed and/or outsourced trials.

Responsibilities:
•Ensure regional/ global clinical operations deliverables progress according to agreed upon timelines and milestones as leader of the Study Management Team (SMT). This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor set up activities as assigned.
•Set-up country budgets and monitor actuals vs forecast for Out of Pocket Expenses, and review assigned vendor invoices/spend.
•Establish enrolment commitments and ensure actual enrolment meets projected commitments across the regions at the clinical tial level.
•Create and update study-specific documents such as Monitoring Guidelines, Informed Consent Form.
•Act as the primary contact person for the local teams within organization.
•Establish and maintain excellent working relationships with internal stakeholders, including Local Trial Managers.
•Ensure compliance with global health authority regulations and guidelines and internal operating procedures and processes.
•Participate in preparation for, and conduct of, Health Authority inspections and internal QA audits.
•Management of global vendors.

Requirements:
•Life science degree (preferable)
•Minimum of 5 years clinical trial management experience from start- up to database lock (on regional and global level) in the pharmaceutical industry or CRO
•Experience with supervision of CROs/vendors is preferred
•Strong decision-making and communication/collaboration skills
•Effective leadership skills

What is offered:
•A challenging CTM role in an international Pharmaceutical company
•You will enjoy highly competitive compensation and a car allowance
•Largely Home Office Based
•Friendly work atmosphere in a great team
•Contribution to pension scheme
•Travel time = work time

Why this role is right for you:
We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a companies dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.

Interested? Please submit your CV via www.docsglobal.com or iris.brouwer@docsglobal.com. We are looking forward to your application.

#PMjob

DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry. 

 

Our Values

At DOCS, we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are:

OUR PEOPLE: We attract, source, develop and retain the best talent to enables us provide world-class people and solutions for our clients.

EXCELLENCE: We never stop looking for new, better ways of working.

ACCOUNTABILITY: We take responsibility for our actions, owning our client’s problems and proactively looking for solutions.

INTEGRITY: Becoming a trusted partner means being honest, respectful and ethically sound, at all times.

OPENNESS: We encourage and facilitate an open and inclusive environment for a diverse global network of employees and stakeholders.

Contact Us
  • 2 Globeside
  • Globeside Business Park
  • SL7 1HZ
  • United Kingdom
  • +44 (0) 2380 688500
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