Global Director, Clinical Project Management

SystImmune is a leading and well‑funded clinical‑stage biopharmaceutical company with operations in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments through bi‑specific, multi‑specific antibodies and antibody‑drug conjugates (ADCs).

We are seeking a highly skilled and motivated Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation to completion, ensuring regulatory compliance, managing timelines and budgets, fostering effective communication among stakeholders, and delivering high‑quality data. This position requires onsite hybrid work in Princeton, NJ.

Responsibilities

• Oversee the planning and execution of global clinical trials
• Develop and implement study protocols, timelines, and budgets
• Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout
• Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines
• Coordinate with cross‑functional teams, including investigators, vendors, and regulatory bodies
• Monitor trial progress and manage data collection to ensure accuracy and integrity
• Identify and mitigate project risks
• Oversee a team of regional CPMs, CRAs and CTAs
• Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice
• Conduct regular meetings with study teams and provide updates to stakeholders
• Coordinate with external vendors and partners involved in the trial
• Support development of key process initiatives and SOPs internally
• Oversee vendors supporting trial execution

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or a related field
• Minimum of 10 years of experience in clinical trial management, including at least 5 years in a direct line management role
• Strong understanding of GCP and regulatory requirements
• Excellent organizational and project management skills
• Proven ability to lead cross‑functional teams and manage multiple priorities
• Strong communication and interpersonal skills
• Ability to work collaboratively in a team‑oriented environment
• Flexibility and adaptability to changing priorities and workload
• Master’s degree in a related field or clinical research certification (e.g., ACRP or SOCRA)
• Experience with electronic data capture (EDC) systems and clinical trial management software
• Prior experience in running or supporting Oncology clinical trials a plus
• Previous experience in a sponsor or CRO environment

Location / Travel

• Princeton, NJ – onsite office
• Overnight travel ~25%

Compensation and Benefits

Base salary range: $180,000 – $230,000 annually, based on qualifications and experience.

• 100% paid employee premiums for medical, dental, and vision coverage
• Supplemental insurance: STD, LTD
• 401(k) plan with 50% company match up to 3% and a vesting schedule of 5 years
• 15 paid time off days per year, sick leave, and 11 paid holidays
• Other benefits may be offered at the company's discretion

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.