Gco Analyst II

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GCO Analyst II
The candidate will assist less experienced research teams with clinical trials budgeting, pricing, clinical space and other aspects of actualizing trials at FH and/or CHW to increase the ability to carry out clinical trials and initiate trials in a timely fashion. Serve as the GCO point of contact for all units (department, division, institute or center), performing pre-award and non-financial post-award activities associated with for-profit clinical grants, contracts, cooperative agreements, and multi-party consortiums. Activities associated with this function include: Serve as the firm Research Office point of contact and liaison for sponsoring organizations. Draft, review, negotiate and process of the following agreements and related amendments/modifications: Industry supported clinical trial agreements, research agreements and complex extramurally funded contracts; non-disclosure and confidentiality agreements; inbound and outbound material transfer agreements; inbound and outbound data use agreements; consortium member agreements. Responsible for the interpretation and articulation of institutional and sponsor policies and procedures to ensure compliance and proactively keeping department apprised of changes in policies and regulations of relevant granting agencies. Work with departments and central administrative offices to achieve compliance. Assist in identifying, developing and implementing process improvements that impact the day-to-day operations of the GCO unit and the firm research enterprise. Partner with other GCO analysts and firm stakeholders in a collaborative, team-based environment. Participating in team-based projects, as assigned. Bachelor’s degree is required. Should have 5+ years’ pqe. JD, Master’s or advanced degree preferred.

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