Sr Director, Clin Research

Date Posted: 4/30/2026

Senior Director, Clinical Research, Board Certified MD
Northern, NJ (3 days onsite)

We are seeking a physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician, Senior Director, Clinical Research. In this role, you will play a pivotal part in advancing our oncology and/or non-oncology pipeline by providing medical expertise, leadership, and operational oversight for a clinical development study(ies).

About You:
You are a highly accomplished professional who excels in the development and execution of clinical projects. As a key member of the cross-functional Development Teams and the Clinical Study Teams, you will employ your expertise in clinical development to advance new therapies to patients in need. Your dedication to scientific rigor and meticulous attention to detail is evident in all your work. With a deep passion for creating important new medicines, you are committed to advancing the field of medical research and improving patient outcomes. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey or California offices to ensure effective collaboration and high-quality execution of your clinical work.

What You’ll Do in partnership with your Manager:
Design and conduct early-stage or late-stage clinical development trials as needed, including, but not limited to assessing clinical safety and efficacy data, performing medical monitoring, and be responsible for other study-related clinical activities. Interpret reports, and prepare oral and written results of product research. Be proactive in fulfilling your responsibilities and pay particular attention to quality and accuracy of work as well as timeliness of deliverables. Collaborate closely with relevant functions including discovery, translational and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, and regulatory personnel. Work closely with functional partners (Clinical Science, Data Management, Clinical Operations, Biostatistics) to ensure an integrated approach to flawless execution and systematic oversight of study protocol(s) in clinical development. Work closely with functional partners to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion.

Qualifications:
MD or DO degree with significant experience in Oncology. Minimum of 5-7 years of clinical experience, including 3+ years in drug development. Experience in clinical practice with direct patient care. Proven track record in leading clinical trials, including medical monitoring of early and late stage clinical trials. In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements. Ability to work effectively in a matrixed environment. Strong analytical, organizational, and problem-solving skills. Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. Passion for clinical trials and improving patient outcomes. Experience with IND and/or NDA/BLA filings is preferred.

The expected salary range for this role is $270,000 to $294,500 depending on skills, competency, and the market demand for your expertise.

Please contact Darren Gutowski at dgutowski@clarkdavis.com