ResponsibilitiesReview 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
QualificationsMinimum 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
Visit Careers at Greenphire