Contract Specialist

2 weeks ago

New Hyde Park, United States Hackensack Meridian Health Full time

Description:

Our team members are the heart of what makes us better.

At Hackensack Meridian Health we help our patients live better, healthier lives and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. Its also about how we support one another and how we show up for our community.

Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.

As the Contract Specialist, the fundamental mission of the Department of Research is to facilitate and promote the research endeavors of investigators at HackensackUMC. The Department provides oversight and management of sponsored projects, and ensures compliance with institutional and sponsor policies and expectations.

Responsibilties:

A day in the life of a Contract Specialist at Hackensack Meridian Health includes:

  • Provides services to investigators conducting clinical trials at HackensackUMC.
  • Responsible for editing, negotiating, and executing industry sponsored clinical trial contracts.
  • Provides professional consultation, advice, and direction to all levels of HUMC staff and corporate sponsors regarding contracting issues such that HUMC clinical trial contracts will best meet legal sufficiency, risk management and financial requirements for the HUMC research objectives.
  • Continually seeks opportunities to improve contracting processes as well as improve customer service.
  • Responsible for handling material transfer agreements, confidentiality agreements, licensing agreements and conflict of interest compliance related to the research efforts of HUMC investigators.
  • Conducts initial intellectual property (IP) analysis and notifies the Office of Commercialization and Technology Ventures of any potential IP, for further analysis.
  • Reviews and coordinates approvals for press release forms, IP release forms and other miscellaneous and legal documents, as required by outside research collaborators.
  • Reviews and analyzes outside agreements for multi-party/multi-funded research projects.
  • Reports to the Manager of Clinical Trials Office.

Qualifications:

Education, Knowledge, Skills and Abilities Required:

  • Either a Bachelor Degree in science or business or a paralegal certificate.
  • Excellent communication skills, and the ability to interpret, convey, explain, and uphold regulatory and institutional requirements.
  • Ability to multitask and to handle a high volume throughput in a timely manner.
  • Demonstrated ability to accurately comprehend and interpret medical and scientific terminology, concepts, and methodology.
  • Advanced computer and spreadsheet skills.

Education, Knowledge, Skills and Abilities Preferred:

  • Minimum of two years of experience in clinical trial contracts negotiation.
  • Thorough understanding of budgeting principles and procedures, and FDA and state regulatory requirements in regard to clinical trials.

If you feel that the above description speaks directly to your strengths and capabilities, then please apply today

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