Director/Senior Director, Clinical Development

SystImmune; Princeton (NJ); On-site; USD 230,000 - 300,000; Full time

Benefits offered by this job

Medical/dental/vision premiums paid

STD/LTD coverage

401(k) with company match

Job summary

SystImmune in Princeton, NJ is seeking an experienced Director/Senior Director of Clinical Development to lead design, execution and interpretation of oncology trials. You will collaborate across functions to deliver high-quality data supporting product development and regulatory submissions.

The ideal candidate holds MD, has 2+ years in medical monitoring of oncology trials, and will oversee safety, data integrity, and regulatory compliance while advancing ADC/biologic programs.

Qualifications

• MD or equivalent required with oncology clinical trial experience.
• Minimum 2 years in medical monitoring of oncology trials; phase 1/2 required, phase 3 preferred.
• Proven track record in clinical development and regulatory submissions, with biologics/ADCs.

Responsibilities

• Lead the design and implementation of clinical development programs across product lifecycle.
• Oversee execution and integrity of clinical trials with enrollment, timelines, and milestones.
• Monitor trial safety in coordination with Safety team and SAE reporting compliance.
• Drive development and scientific accuracy of protocols, CSRs, and regulatory submissions.
• Act as medical lead on study teams and represent clinical strategy in regulatory interactions.

Skills

Medical monitoring

Clinical development

Regulatory knowledge

GCP/compliance

Biologics/ADC experience

Education

MD or equivalent

Job description

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.

SystImmune is seeking an experienced Director/Senior Director of Clinical Development to lead the direction, planning, execution, and interpretation of clinical trials within the Clinical Development program. This person would also collaborate across functions to deliver high-quality clinical data that supports product development, regulatory submissions, and business strategy.

Key Responsibilities

• Lead the design and implementation of clinical development programs grounded in sound medical and scientific principles, regulatory knowledge, and business objectives. Provide strategic medical input across the product lifecycle from early development through phase 3, for both internal and partnered programs
• Oversee the execution and integrity of clinical trials. Collaborate with Clinical Operations to manage enrollment progress, timeline adherence, and delivery of key milestones. Proactively monitor trial safety in coordination with the Safety team, ensuring compliance with serious adverse event (SAE) reporting requirements
• Drive the development and scientific accuracy of key clinical documents, including protocols, Investigator Brochures, Clinical Study Reports (CSRs), regulatory submissions, and response packages
• Serve as the medical lead on clinical study teams , aligning medical strategy across functions. Act as a key clinical representative in regulatory interactions and ensure adherence to GCP, pharmacovigilance standards, SOPs, and global compliance requirements
• Provide in-house clinical expertise on assigned compounds and indications. Actively engage with investigators and opinion leaders to inform development strategy and protocol design. Stay current on therapeutic area developments through continuous learning and participation in scientific forums

Qualifications

• M.D. or equivalent (international degrees accepted)
• Minimum of 2 years of experience in medical monitoring of oncology clinical trials; phase 1/2 required, phase 3 experience preferred
• Prior experience in clinical development or pharmaceutical/biotech settings
• Proven track record in product safety oversight and clinical trial execution, particularly with biologics such as ADCs and immune-oncology agents
• Strong foundation in clinical and drug development processes
• Sound medical judgment with expertise in medical safety data interpretation

Compensation and Benefits:

The expected base salary range for this position is $230,000 - $300,000 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.