Duration & Type: 9+ months Contract with a major pharmaceutical industry client

Location: Remote

Responsibilities:

• Independently negotiates and finalizes Clinical Trial Agreement and Clinical Trial Amendments to include protocol budgets, PI changes, fixed costs, contract assignments, site/payee name change, terminations, extensions and IRB task orders.
• Develop Site Clinical Trial Agreements, budgets, amendments and task orders.
• Develop study budget utilizing the benchmark cost.
• Independently negotiate and execute Site Clinical Agreements and budget amendment with minimum supervision.
• Evaluate and benchmark Investigational sites budget requests for fair market value
• Work with amendment requestor to ensure amendment integrity prior to negotiation.
• Maintain proactive communication with Payments team to ensure payment reconciliation prior to contract termination.
• Liaison/collaborate with Clinical Study Manager, Investigational Sites, Legal, Compliance, Patent, insurance and study start up groups to expedite and finalize contracts and amendments.

Required:

• Education: Degree in business administration, legal, finance, science or related field or equivalent on the job experience may be considered.
• 3+ years of contract management and/or study start up activities including contract and budget negotiations.
• Experience in pharmaceutical services a plus.
• High degree of organizational, analytical, and team management skills.
• Computer literacy with document and spreadsheet applications. Ability to work on complex, multi-faceted projects.
• Excellent negotiation skills and vast knowledge of clinical trial agreements
• Language: Fluent English (oral and written)

For consideration, please send resume to career@infoquestgroup.com