Job Description
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 [email protected]
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