Clinical Project Manager II – Oncology, Gynecologic Malignancies

Syneos Health

Clinical Project Manager II overseeing oncology clinical trials at Syneos Health. Focused on gynecologic malignancies and operational execution in a remote setting.

Posted 6/5/2026full-timeRemote • Maine, Montana, North Carolina, Ohio, Rhode Island • 🇺🇸 United StatesJuniorMid-Level💰 $95,000 - $175,700 per yearWebsite

ATS Keywords

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Hard Skills

clinical trial operationsclinical project managementvendor managementstudy timeline managementdata reconciliationclinical supplies planningstudy closeout activitiesOncologyGynecologic Malignancy clinical trialsICH-GCP

Soft Skills

collaborationcommunicationorganizational skillsleadershipproblem-solvingattention to detailtime managementadaptabilityinterpersonal skillsmatrix environment effectiveness

Tools & Technologies

Microsoft Officeproject management tools

Industry Keywords

pharmaceuticalclinical drug developmentbiopharmaCROSMOclinical research sitetrial unitclinical research processesstudy milestonesclinical objectives

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the Study Lead and cross-functional study team in day-to-day clinical trial operations
Support activities such as: Clinical Trial Team (CTT) meeting coordination and minutes, Clinical supplies planning and tracking, Lab specimen tracking and reconciliation, Imaging data reconciliation, Study status reporting and updates, Study closeout activities
Contribute to single or multiple studies, depending on scope and complexity
Lead smaller or limited-scope studies, as appropriate (e.g., survival follow-up studies)
Track and manage study timelines using project management tools
Collaborate with internal stakeholders and external partners, including investigative sites, vendors, and committees
Support achievement of study milestones and clinical objectives

Requirements

What you’ll need

Minimum 2 years of pharmaceutical and/or clinical drug development experience within the last 5 years (e.g., biopharma, CRO, SMO, hospital, clinical research site, or trial unit)
Clinical Project Management experience in Oncology is required
Direct experience supporting Gynecologic Malignancy clinical trials is required
Vendor management experience is required
Strong working knowledge of clinical trial operations and execution
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Good understanding of ICH-GCP and clinical research processes
Ability to work effectively in a matrix environment

Benefits

Comp & perks

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