Syneos Health · 5 hours ago
Project Manager II: Late Phase Oncology; ISR/CO Study Manager (Sponsor Dedicated/ US Remote)
United States
Full-time
Remote
Mid Level
$95K/yr - $176K/yrSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. The Project Manager II will manage a portfolio of Investigator Sponsored Research (ISR) and collaborative studies, ensuring compliance and timely progression while partnering closely with Medical Affairs and investigators.
BiotechnologyHealth CarePharmaceuticalTherapeutics
Responsibilities
Manage a high volume of global ISR and collaborative studies, ensuring compliance, scientific integrity, and timely progression
Serve as the primary operational contact for principal investigators and study teams, providing ongoing support from start‑up through completion
Ensure accurate tracking of study status, milestones, documentation, and deliverables across the ISR/CO portfolio
Partner with Medical Affairs to facilitate study progress, troubleshoot issues, and remove barriers to execution
Support investigators through the publication process, including data requests, review timelines, and coordination with internal stakeholders
Oversee study budgets, financial tracking, and forecasting for assigned ISR/CO programs
Monitor potential risks related to funding, operations, timelines, and compliance; escalate and mitigate proactively
Review and approve site/vendor invoices and support client billing with accuracy and accountability
Represent Syneos Health as a key point of contact in this high‑visibility, customer‑facing role
Build strong working relationships with Medical Affairs, sponsors, and investigators to ensure alignment and clarity of expectations
Lead internal/external meetings with confidence—driving communication, organization, and follow‑through
Participate in protocol‑specific onboarding and study‑related training
Continue to deepen your expertise in oncology and late‑phase research
Share knowledge and best practices with peers and cross‑functional teams to elevate study execution standards
Qualification
Required
Prior experience managing ISR/CO studies within a pharmaceutical or CRO environment
Oncology experience required, ideally late-phase
Strong understanding of ICH GCP, ethics, regulatory expectations, and clinical research operations
Exceptional communication, organization, and time management skills—this role is highly visible and investigator-facing
Ability to manage multiple simultaneous studies, prioritize effectively, and work independently
Proficiency in MS Office and comfort working in a dynamic, fast-paced environment
Benefits
Company car or car allowance
Health benefits to include Medical, Dental and Vision
Company match 401k
Eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
Flexible paid time off (PTO) and sick time
Company
Syneos Health
Syneos Health, the only fully integrated end-to-end clinical and commercial solution organization.
Founded in 1985
10001+ employees
H1B Sponsorship
Syneos Health has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (35)
2024 (26)
2023 (49)
2022 (63)
2021 (84)
2020 (63)
Funding
Current Stage
Public CompanyTotal Funding
$524.65M2023-09-28Private Equity
2023-05-10Acquired
2021-03-01Post Ipo Secondary· $524.65M
Leadership Team
Costa Panagos
Chief Executive Officer
Michael Bonello
Executive Vice President and Chief Financial Officer
Recent News
2026-01-09
Company data provided by crunchbase