Clinical Payment Associate
Clinical Payment Associate
Participating as Integral contributor to a Team Environment.
Perform activities required for vendor outsourcing contracting administration and BUCA responsibilities.
Review Invoice and PO trackers as provided by Accounting System (Coupa) and analyze for business follow-up as needed.
Create business friendly reporting from status reports from the different systems provided.
Update and manage different trackers for contracts, POs, payments, and other activities as required.
Preparation, participation, and follow-ups to Vendor and/or study Finance meetings.
Execute other responsibilities as needed and requested to accomplish the COST business objectives.
Contributor to COST process innovations in a collaborative and growth mentality environment.
Process, negotiate, prepare and route non-disclosure agreements for signature.
Assist in processing, negotiating, preparing and routing other agreement type when requested.
BS degree or equivalent degree/experience. Minimum of 2 years clinical/vendor payment experience in the pharmaceutical or biotech industry, preferably the majority in oncology drug development.
Minimum 2 years vendor and contract payment experience with a sponsor company or CRO managing various phase clinical trials.
Understanding of the drug development process.
Motivated self-starter who can work in a fast-paced environment.
Creative problem solver with good communication and written skills.
Strong interpersonal and organizational skills are needed, with a high degree of attention to detail.
Proficient with the MS Office Suite especially Excel.
Ability to work with minimal direction.
Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team is extremely important.
Has familiarity working with vendor contracting systems/portals.
Knowledge and/or familiarity with Ex-US region(s) clinical trial site PO/Invoice systems.
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