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Clinical Project Manager

Meeting Protocol Worldwide Dallas ,TX
  • Posted: over a month ago
  • $65,000 to $75,000 Yearly
  • Full-Time
  • Benefits: 401k, dental, medical, vision
Job Description

ROLE
The Clinical Project Manager will perform a wide variety of activities to support the start-up, management, and completion of patient services for clinical research studies. They will report directly to the Vice President, Patient Services and will manage sponsors and vendors, and deliver project activities on time. This is a full time, work from home position.

Responsibilities of this position include but are not limited to:

  • Contracts support
  • Review budget estimates as needed
  • Proof contracts for accuracy
  • Proof slide decks
  • Study management activities and study start-up
  • Maintain activities spreadsheet for studies
  • Regular communication with global study stakeholders including CRO and Sponsor project
  • Oversee scheduling and conduct study on-boarding phone calls
  • Collaborate on operational internal policies and manage adherence
  • Create study-specific patient and site-facing documentation
  • Ongoing administrative tasks and document management throughout the life of the study
  • Liaise with Finance to produce statements, reports, and invoices and send monthly
  • Serve as an additional Subject Matter Expert for Scout software development team
  • The ideal candidate will have the following experience, skills and knowledge:
  • Strong understanding of project management
  • Strong understanding of the clinical trial process
  • Ability to handle multiple projects in various planning stages concurrently
  • Ability to track and manage key dates / deadlines
  • Ability to read and understand clinical trial protocols
  • Experience with medical/technical writing

The ideal candidate will have the following competencies and qualities:

  • Bachelor’s Degree
  • Experience as a Study Coordinator or Site Manager is preferred
  • Strong computer skills (Excel, Word, Outlook)
  • The ability to learn/coachable
  • Timely, professional, courteous communication with clients, vendors and colleagues
  • Highly ethical and of good character
  • Attention to detail
  • Well organized with an ability to prioritize and multi-task
  • Ability to work within and meet strict deadlines
  • Ability to work under pressure in a fast paced, demanding environment
  • Self-motivated but also follows instructions
  • Good work ethic
  • Forward thinking / problem solver / critical thinker / analytical
  • Team player
Company Description
Meeting Protocol Worldwide, L.P. (MPW) was formed to provide services exclusively for the clinical research and pharmaceutical industry. In the twenty five years since its establishment, MPW provides services for hundreds of pharmaceutical, biotech, medical device manufacturers and clinical research organizations in over 100 countries around the world.

Meeting Protocol Worldwide

Meeting Protocol Worldwide, L.P. (MPW) was formed to provide services exclusively for the clinical research and pharmaceutical industry. In the twenty five years since its establishment, MPW provides services for hundreds of pharmaceutical, biotech, medical device manufacturers and clinical research organizations in over 100 countries around the world.

Address

15770 Dallas Parkway
Dallas, TX
USA

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