Contracts & Grants Analyst *** Belgium *** Home based / Office based

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

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Discipline
Finance / Administration, Contracts / Proposals
Hours
Full Time
Contract Type
Permanent
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Description:

• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator initiated studies through direct negotiation with Clinical Trial Sites
• Responsible for delivery against established targets/measurements
• Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required
• Participate in discussions related to the development of site/investigator budgets aligned with fair market value
• Manage the contract amendment life-cycle
• Work with the global C&G team as necessary to review and analyze contractual terms to reach resolution. Assess risks of budget and legal provisions in conjunction with members of the C&G team and support functions. Escalate issues as appropriate
• Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites
• Assume responsibility for all aspects of legal document and metrics tracking
• Provide support to review, authorize and/or understand aspects of site payments. Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines
• Adhere to SOPs, ethics and departmental compliance as determined by departmental management as well as operating companies, corporate, HCC and QA guidelines. Ensure familiarity with departmental and appropriate corporate processes
• Comply with requests from QA and auditors

Education & Experience

• Bachelor's or Master's degree in appropriate scientific or business discipline
• 3 years' experience and/or equivalent competencies in legal/pharmaceutical industry/clinical research
• Excellent communication skills (both oral and written) in English & Dutch, French is a plus
• Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.) a plus
• Working knowledge of PCs (MS Office suite at a minimum) and database management
• Previous experience working in virtual teams preferred

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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