Remote Oncology Clinical Project Leader

Theradex Systems, Inc.; Princeton (NJ); On-site; USD 105,000 - 165,000; Full time

Benefits offered by this job

Medical benefits

401(k) match

Tuition reimbursement

Generous vacation/sick leave

Flexible work schedules

Employee discounts

Job summary

Theradex Systems, Inc. is seeking a Clinical Project Manager or Senior Clinical Project Manager to lead global oncology trials from feasibility to closeout.

The position emphasizes cross-functional leadership, risk management, and QA collaboration, with a focus on timelines, budgets, and study quality. Ideal candidates have 4+ years in clinical research, strong Excel/MS Office skills, and oncology trial experience.

Qualifications

• BS in life sciences or equivalent (RN included).
• MS or PhD preferred.
• 4+ years in clinical research with successful trial site management.
• Proficiency with Excel and MS Office; able to master CTMS/electronic platforms.
• Oncology trials experience and CAR-T/gene therapies is highly preferred for senior PMs.
• CRO/pharma environment experience preferred for senior PMs.
• Must be fluent in English (written and spoken).

Responsibilities

• Lead clinical projects and guide cross-functional teams.
• Monitor enrollment, retention, and study metrics; drive recruitment strategies.
• Identify operational risks and implement mitigation plans (CAPA).
• Manage TMF and support audits with QA.
• Oversee budgets and timelines; manage invoices and COs as needed.
• Lead day-to-day study team activities and training.

Skills

Clinical trial management

Budget & timelines

Quality & CAPA

Team leadership

Communication

Problem solving

Education

BS in life sciences (includes RN)

MS or PhD preferred

Project management experience

CRO/pharma experience

English fluency

Tools

Excel

MS Office

Electronic trial platforms / CTMS

Job description

Theradex Systems, Inc. is seeking a Clinical Project Manager or Senior Clinical Project Manager to lead global oncology trials from feasibility to closeout.

The position emphasizes cross-functional leadership, risk management, and QA collaboration, with a focus on timelines, budgets, and study quality. Ideal candidates have 4+ years in clinical research, strong Excel/MS Office skills, and oncology trial experience.