Associate Director, Clinical Project Management - Oncology

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Bothell, 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

Associate Director, Clinical Project Management (CPM)

to join our dynamic team. The successful candidate will oversee and coordinate global 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 Associate Director, Clinical Project Management will play a critical role in delivering high-quality data and ensuring the success of clinical studies.

This position requires

onsite hybrid work model 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 7 years of experience in clinical trial management with a preference of leading Clinical Operations team (CRA, SSU, CTM).

Experience in managing global oncology trials

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 in office

Overnight travel ~25%

Compensation and Benefits:
The expected base salary range for this position is

$150,000- $180,000

annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.

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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