Clinical Project Manager II – Oncology, Gynecologic Malignancies

🔥 0 minutes ago

🦞 Maine, North Carolina, +3 more states – Remote

🦞 Maine – Remote 🌲 North Carolina – Remote 🏈 Ohio – Remote 🏰 Missouri – Remote ⚓ Rhode Island – Remote

💵 $95k - $175.7k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• 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

• 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

• 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