Clinical Project Manager II Virology Sponsor Dedi
Job
Syneos Health inVentiv Health Commercial LLC
Remote
Full-Time
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Job Description
Clinical Project Manager II
- Virology (Sponsor Dedicated/Remote) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.
- for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture
- where you can authentically be yourself. Central to this is our purpose
- Driven to Deliver
- which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job ResponsibilitiesClinical Project Manager II
- VirologySponsor Dedicated | Remote (Preference for Foster City, CA-Based Candidates) Are you a Clinical Project Manager who thrives in fast-paced, collaborative environments and enjoys driving complex clinical trials forward with confidence and precision?
THE ROLE
As a Clinical Project Manager II- Virology, you will oversee operational delivery and vendor management activities for early-phase virology clinical trials.
WHAT YOU WILL DO
Lead and support operational execution of Phase I virology clinical trials within a sponsor-dedicated model Manage and oversee vendors to ensure quality deliverables, timelines, and study expectations are consistently met Coordinate cross-functional clinical trial activities from study start-up through closeout with minimal oversight Drive meeting leadership by setting agendas, facilitating productive discussions, documenting decisions, and ensuring accountability for action items Partner closely with Clinical Operations, study teams, vendors, and stakeholders to proactively identify and resolve operational challenges Ensure effective communication across teams while maintaining professionalism and strong stakeholder relationships Monitor study progress, timelines, risks, and operational deliverables to support successful trial execution Contribute to a positive, collaborative team culture built on transparency, accountability, and mutual respect Support inspection readiness and compliance with applicable SOPs, GCP, and regulatory requirements Lead with a solutions-oriented mindset while helping align teams toward shared project goalsWHO YOU ARERequired Qualifications Clinical Operations experience or related clinical trial management knowledge Prior experience supporting or managing clinical trials within a CRO, biotech, or pharmaceutical environment Strong vendor management and oversight experience Understanding of the full clinical trial lifecycle and operational processes Experience coordinating cross-functional teams and driving project execution Strong organizational, communication, and meeting facilitation skills Ability to work independently, prioritize effectively, and proactively navigate challenges Professional presence with strong emotional intelligence and stakeholder management capabilities Preferred Experience Early-phase (Phase I) clinical trial experience Virology therapeutic area experience strongly preferred Stable career progression demonstrating depth in clinical trial management Experience working in sponsor-dedicated environments Ability to lead discussions confidently in fast-paced, high-visibility settingsWHAT MAKES THIS
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