Responsibilities

*        Review and interpret global clinical payment documents.  (Contracts, budgets, amendments, and ICFs)
*        Ensure that data is extracted from the source document(s) and uploaded accurately into the software timely
*        Collaborate and communicate with business partners to verify interpretation of contracted terms and rates for accuracy
*        Adhere to auditing and monitoring checklists and procedures
*        Consult in the dprogram to support interpretation and implementation activities
*        Identify industry trends affecting clinical trials and develop understanding of common therapeutic and country-specific nuances specific to payment schedule design
*       Perform other duties, assignments, and/or special projects as time or circumstances necessitate

Qualifications

*        Minimum of 1-2 years in the pharmaceutical or CRO industry with a minimum of 1 year of contract management related experience preferred.
*        Foundational background on global clinical trial design preferred.
*        Ability to dissect the key elements of trial budgets, including therapeutic phase and country-specific variances.
*        Ability to handle high volume of contract activity in a fast-paced environment
*        Excellent writing skills.
*        Must have excellent analytical, organizational, interpersonal and time management skills.
*        Experience with Microsoft Word and Excel required.
 

This is a full time position

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