We know why you are reading about this opportunity. You are driven to achieve goals. You are looking to make a direct impact. You want to work in a culture where your co-workers work as part of a diverse team, communicate across departments, and have a positive attitude. If we had to guess, you are innovative with great ideas, want to bring efficiencies to processes, and are looking to grow your career. Are we right? If so, let’s talk about who we are.

Who We Are
Greenphire is a leading provider of clinical payment and communication solutions. We provide software as a service (SaaS) to reduce costs, increase participant retention, and produce quantifiable results for our clients in the clinical trial industry. Our vibrant culture focuses on four key values: All In, As a Team, For a Purpose, Solving Problems.

We are a multi-year recipient of the Philadelphia Business Journal’s Best Places to Work award, and love to give shout-outs and awards to our employees. Our For A Purpose committee champions philanthropic activities throughout the year so employees can give back to our community. We have a diversity committee that focuses on breaking down barriers, recognizing that our uniqueness is what makes us so successful!

How You Will Contribute
  • 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 design and delivery of a training program 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

For Consideration You Will Have
  • Previous experience in the pharmaceutical or CRO industry required with 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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