Systimmune
SystImmune 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). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND‑enabling stages, representing cutting‑edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
Global Director, Clinical Project Management (CPM) The successful candidate will oversee and coordinate global clinical trials from initiation through to completion, ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. This role involves ensuring complianceUs with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The global Director, Clinical Project Management will play a critical role in delivering high‑quality data and ensuring the success of clinical studies.
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 hybrid – 3 days in office
Overnight travel ~25%
Compensation and Benefits The expected base salary range for this position is $180,000–$230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to 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 exceeds the requirements of the role.
We offer a comprehensive benefits package including 100% paid employee premiums for medical, dental and vision; STD, LTD; a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years; 15 PTO days per year, sick leave, plus 11 paid holidays and more.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
#J-18808-Ljbffr
Global Director, Clinical Project Management (CPM) The successful candidate will oversee and coordinate global clinical trials from initiation through to completion, ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. This role involves ensuring complianceUs with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The global Director, Clinical Project Management will play a critical role in delivering high‑quality data and ensuring the success of clinical studies.
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 hybrid – 3 days in office
Overnight travel ~25%
Compensation and Benefits The expected base salary range for this position is $180,000–$230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to 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 exceeds the requirements of the role.
We offer a comprehensive benefits package including 100% paid employee premiums for medical, dental and vision; STD, LTD; a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years; 15 PTO days per year, sick leave, plus 11 paid holidays and more.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
#J-18808-Ljbffr