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
  • Conduct mid-study audits to ensure compliance with configuration specifications and requirements. 
  • Conduct end of study quality checks
  • Liaise between PM/PS team and Implementation and Verification Teams in communicating processes and procedures
  • Consult with PM/PS teams in complex or special requests regarding study/site set ups or changes to ensure appropriateness and root cause
  • Document implementation and verification processes
  • Develop and monitor controls to ensure standard process and procedures among the Implementation and Verification Teams
  • Establish new and enhance current auditing and monitoring checklists and procedures
  • Train/onboard new hires
  • Design, develop, and deliver 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 budget-design
  • Assist in the roll out of new technologies to the Implementation and Verification Teams
  • Perform other duties, assignments, and/or special projects as time or circumstances necessitate

For Consideration You Will Have
  • Bachelor’s Degree preferred, or equivalent work experience and/or training
  • Previous contract management related experience within pharmaceutical or CRO arena
  • Foundational background on global clinical trial design, contracts and budget
  • Strong experience with Microsoft Excel required
  • Client and process focused
  • Strong leadership skills required
  • Ability to challenge and improve on existing practices and identify and develop new practices to address gaps
  • Must have excellent analytical, organizational, interpersonal and time management skills

Visit Careers at Greenphire

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