Sponsor-Driven Clinical PM Remote (US) Inflammation

Syneos Health/ inVentiv Health Commercial LLC

Arizona

Remote

USD 120.000 - 160.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Syneos Health is seeking an Experienced Clinical Project Manager for an inflammation program. This sponsor-dedicated, remote- US only role oversees study execution from start-up to closeout with hands-on leadership in a fast-paced environment.

The ideal candidate has 3+ years of clinical project management experience, strong CRO/vendor oversight skills, and a proven ability to drive study progress while coordinating cross-functional teams across global partners.

Qualifikationen

  • 3+ years of clinical project management experience.
  • Experience running trials from start-up through closeout.
  • Experience supporting complex Phase 2b studies within inflammation.
  • Strong CRO/vendor management experience.
  • Ability to drive study execution in fast-paced environments.

Aufgaben

  • Drive operational execution of a complex Phase 2b inflammation study from start-up through closeout.
  • Independently manage day-to-day study operations with minimal oversight.
  • Own timelines, deliverables, risks, and issue resolution across multiple workstreams.
  • Partner cross-functionally to identify risks and implement operational solutions quickly.
  • Lead vendor management activities and oversight of external partners and CROs.

Kenntnisse

Clinical project management
Cross-functional leadership
Vendor management
Study start-up/closeout
GxP/Regulatory knowledge
Communication skills

Tools

MS Word
MS Excel
PowerPoint

Jobbeschreibung

Syneos Health is seeking an Experienced Clinical Project Manager for an inflammation program. This sponsor-dedicated, remote- US only role oversees study execution from start-up to closeout with hands-on leadership in a fast-paced environment.

The ideal candidate has 3+ years of clinical project management experience, strong CRO/vendor oversight skills, and a proven ability to drive study progress while coordinating cross-functional teams across global partners.

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