Job Details

Senior Contract Budget Specialist

Company name

ABIOMED, Inc.

Organization Type

In-House

Job Type

Legal Staff

Date Last Verified

Aug 16,2019

Valid Through

Nov 29,2019

Posted on

Jul 04,2019

Years of Experience

Min 5 yrs required

Location

Danvers, MA, United States

Employment Type

Full-time

Industry

Legal
Practice Area
Contract Law >> Contract Law
Intellectual Property >> Intellectual Property - Litigation >> Intellectual Property - Litigation - Life Sciences >> Intellectual Property - Litigation - Life Sciences General
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Senior Contract & Budget Specialist
The candidate reports to the Associate Director, Clinical Programs and is responsible for supporting the Clinical Programs team in accelerating the start-up, maintenance and closeout activities of clinical studies through the development and execution of comprehensive budget and clinical contract contracting tools in support of Clinical Programs.Provide specialized study support and assistance to clinical teams and physicians in the preparation, negotiation and execution of all global Clinical Trial Research Agreements and site budgets; in addition to any other site-related documents, such as amendments, addenda, facility use agreements, letters of indemnification, etc. Perform Clinical Trial Site contract review for compliance and/or modification to Abiomed standard template language utilizing departmental tools (e.g. Negotiation Guidelines/reference manual) in order to facilitate and streamline contract review timelines and iterations including reduction of hand-offs to Office of General Counsel. Negotiate master agreements with sites globally as requested.Collaborate with investigator sites, members of Clinical Operations Management and Office of General Counsel to finalize/execute required contracts. Preparation, negotiation and execution of Steering Committee (SC), Data Safety Monitoring Board (DSMB) and Clinical Events Committee (CEC) for all assigned studies in collaboration with Clinical Team stakeholders. Review, approve and administer Site and Vendor payments for all assigned studies. Preparation, negotiation and execution of Steering Committee (SC), Data Safety Monitoring Board (DSMB) and Clinical Events Committee (CEC) for all assigned studies in collaboration with Clinical Team stakeholders.Preparation of study budgets for Worldwide Profit Planning (WWPP) projections for senior management for current and proposed studies. Should have Bachelor’s degree in life sciences. Paralegal preferred. Should have 5+ years of experience in Clinical Trials at a Sponsor or Clinical Research Organization.

Additional info

Requisition ID: 1841

Company info

Hiring Coordinator
ABIOMED, Inc.
22 Cherry Hill Drive
Danvers, MA 01923

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