Clinical Project Manager
Princeton, NJ
Full Time
Manager/Supervisor
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 discover 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.
We are seeking a highly skilled and motivated Clinical Project Manager (CPM) to join 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.
Responsibilities
We are seeking a highly skilled and motivated Clinical Project Manager (CPM) to join 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.
Responsibilities
- 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 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
- 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
Qualifications
- 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 in a team-oriented environment
- Flexibility and adaptability to changing priorities and workload
Preferred Qualifications:
- 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 Hybrid 3days/week. Remote also considered with quarterly visits to Princeton.
- Overnight travel ~25%
Compensation and Benefits:
The expected base salary range for this position is $110,000 - $150,000 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.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also 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.
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