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Form of work
SalaryThe Clinical Contracts Specialist Sr works closely with project, people, and functional leaders across Clinical Operations & Biometrics, Procurement, Legal, Finance, and Suppliers to ensure appropriate contracts are in place for COBM projects and payments associated to contracts are issued to vendors.
DISTINGUISHING CHARACTERISTICS:
This is a job requiring a combination of advanced skills and experience in drafting, negotiating, and finalizing contracts for COBM related services.
Responsibilities
Drafts, reviews and negotiates clinical trial agreements (Master Service Agreements, Work Orders, and Clinical Trial Agreements) and site budgets with US and ex-US institutions.
Evaluate changes in study protocols to determine the impact on clinical trial site budgets; develop, negotiate and finalize budget amendments.
Provide continuing support on executed agreements (e.g., drafting amendments, extensions and terminations, interpreting contractual language in response to issues or questions that arise).
Work closely and communicate with members of the Lifecycle Finance teams and other internal stakeholders; provide timely updates on contract and site budget status', identifying and escalating any potential critical path items as appropriate.
Track, maintain and update assigned contract information within the COBM Clinical Trial Management System (CTMS) and other tracking tools, to ensure completeness and accuracy, as applicable.
Works with Supplier Relationship Manager and Legal to establish Master Services Agreement (MSA) for as many suppliers as possible.
Works with Supplier Relationship Manager to incorporate Key Performance Indicators into contracts for applicable suppliers.
Establish Purchase Orders (PO), review related Invoices, track spend against contracts / PO's, and report spend as necessary.
Other tasks may be assigned from time to time to support overall COBM function.
Other duties as assigned by management.
Education:
(Required) Bachelor's Degree in Business / Finance or industry related field
(Preferred) Master's Degree in Business / Finance or industry related field
Experience:
5 Years of contract drafting negotiation and finalizing experience within Diagnostics & Pharmaceutical Industry.
5 Years of specific RFI,RFP, Contracting and or Budget Management experience.
4 Years of Clinical Trial experience.
Job Types: Full-time, Contract, Temporary
Pay: $30.00 - $50.00 per hour
Schedule:
- Monday to Friday
Ability to Relocate:
- Pleasanton, CA: Relocate before starting work (Required)
Work Location: Remote
