Clinical Project Manager

Syst Immune is a leading and well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi‑specific, multi‑specific antibodies and antibody‑drug conjugates (ADCs). Syst Immune has multiple assets in various stages of clinical trials for solid‑tumor and hematologic indications and a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND‑enabling stages.惦>

We are seeking a highly skilled and motivated Clinical Project Manager (CPM) to החלט our dynamic team. The successful candidate will oversee and coordinate clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The CPM will play a critical role in delivering high‑quality data and ensuring the success of clinical studies.惦>

• Oversee the planning and execution of clinical trials
• Develop and implement study protocols, timelines, and budgets
• Manage all aspects of clinical trial operations including site selection, initiation, monitoring, and close‑out
• Ensure compliance with Good Clinical Practice (GCP)(one of the best) 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
• Prepare and submit regulatory documents and maintain trial documentation
• 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
• Conduct site visits to ensure compliance with protocols

• Bachelor’s degree in Life Sciences, Nursing, or a related field
• Minimum of 5 years of experience in Clinical Trial Management
• 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
  
  AMPLE in a team‑oriented environment
• Flexibility and adaptability to changing priorities and workload

• Master’s degree in a related米奇 field or clinical research certification (e.g., ACRP or SOCRA)
• Experience with electronic data capture (EDC) systems and clinical trial,message) management software
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• Prior experience in running or supporting Oncology clinical trials
• Previous experience in a sponsor or CRO environment

• Princeton Hybrid 3 days per week;
  Remote also considered with quarterly visits to Princeton
• Overnight travel approximately 25%

The expected base salary range for this position is $110,000–$150,000 annually. Actual compensation will be based on a variable set of factors including a candidate’s qualifications, experience, and skills. While most offers typically fall within the low to mid‑point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceed the requirements of the role.

Syst Immune offers a comprehensive benefits package including 100% paid employee premiums for medical, dental, vision, STD, LTD; a 401(k) plan with a 50% company match up to 3% and a vesting schedule of only 5 years; 15 PTO days per year, sick leave, plus 11 paid holidays, and more.

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