Associate Director, Clinical PM – Oncology (Hybrid)

Systimmune; Princeton (NJ); Hybrid; USD 150,000 - 180,000; Full time

Benefits offered by this job

Premium medical/dental/vision coverage

401(k) with company match

Paid time off (PTO)

Job summary

SystImmune in Princeton, NJ, seeks an Associate Director, Clinical Project Management to oversee global clinical trials from initiation to completion. You will ensure regulatory compliance, manage study timelines and budgets, and foster cross‑functional collaboration among investigators, vendors, and regulatory bodies.

The role requires leading a team of CPMs, CRAs, and CTAs, with a strong background in oncology trials and GCP knowledge.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or related field.
• 7+ years in clinical trial management; preference for leading Clinical Operations teams (CRA, SSU, CTM).
• Experience in managing global oncology trials and in sponsor or CRO environments.
• Strong knowledge of GCP and regulatory requirements.
• Excellent organizational and project management skills; ability to lead cross-functional teams.
• Effective communication and interpersonal skills; able to manage multiple priorities.
• Master’s degree or clinical research certification (ACRP or SOCRA) preferred; experience with EDC and CTMS tools.

Responsibilities

• Oversee planning and execution of global clinical trials.
• Develop protocols, timelines, and budgets; manage trial operations from initiation to closeout.
• Ensure GCP compliance and regulatory alignment across sites.
• Coordinate with investigators, vendors, and regulatory bodies; manage data integrity.
• Lead regional CPMs, CRAs, and CTAs; mentor teams.
• Prepare and submit regulatory documents in line with local standards.

Skills

Project management

Cross-functional leadership

Regulatory compliance

GCP knowledge

Stakeholder communication

Team leadership

Education

Bachelor's degree in Life Sciences, Nursing, or related field

Master’s degree or clinical research certification (ACRP or SOCRA)

Tools

Electronic Data Capture (EDC) systems

Clinical Trial Management Software

CTMS

Job description

SystImmune in Princeton, NJ, seeks an Associate Director, Clinical Project Management to oversee global clinical trials from initiation to completion. You will ensure regulatory compliance, manage study timelines and budgets, and foster cross‑functional collaboration among investigators, vendors, and regulatory bodies.

The role requires leading a team of CPMs, CRAs, and CTAs, with a strong background in oncology trials and GCP knowledge.