Medical Director MD Immunology

About The Role

Medical Director, Clinical Development – Immunology

Your Contributions (include, but are not limited to)

• Serve as a key physician and study-level clinical leader for assigned Immunology development programs.
• Independently lead clinical studies while contributing medical and scientific expertise to broader development strategy.

You Will

• Lead design, development, and execution of Phase 1–3 clinical studies with multidisciplinary teams.
• Develop and implement clinical study protocols; contribute to clinical research strategy.
• Serve as Sponsor Medical Monitor; provide medical oversight and make study-level medical/safety decisions.
• Partner with Drug Safety to assess adverse events and support benefit-risk assessment.
• Oversee study execution per Good Clinical Practice, regulations, and company procedures.
• Analyze and interpret clinical data; translate findings into scientific/development insights.
• Contribute to clinical study reports, investigator brochures, and regulatory documents.
• Collaborate to incorporate biomarkers and translational endpoints into development plans.
• Identify and engage clinical investigators, consultants, and external experts.
• Use knowledge of evolving treatment landscape and emerging science for study-level decisions.
• Collaborate across functions to evaluate opportunities and inform clinical research plans.
• Communicate study progress, risks, and recommendations to teams and senior leaders.

Requirements

• MD or DO with accredited residency training and board certification in a relevant clinical specialty.
• 2+ years of clinical research and development experience (Phase 1–4) in pharma/biotech or clinical research/academic setting.

Experience That Will Help You Thrive (preferred)

• Clinical expertise in gastroenterology, dermatology, or other immune-mediated disease specialty.
• Medical Monitor and/or Study Lead experience for industry-sponsored trials.
• Experience designing studies/protocols (endpoints, eligibility, dose strategy).
• Early clinical development experience; translating preclinical/translational findings.
• Phase 2/3 experience in immune-mediated diseases.
• Experience interpreting efficacy/safety/biomarker/pharmacology data.
• Knowledge of global drug-development requirements, GCP, and regulatory expectations.
• Experience contributing to regulatory documents and interacting with health authorities.
• Experience engaging investigators, external experts, CROs, and partners.
• Ability to influence and lead cross-functional teams without direct reporting authority.

Benefits/Compensation

• Annual base salary: $254,600.00–$347,000.00; annual bonus (target 35%); eligibility for equity long-term incentive.
• Retirement savings plan (with company match), paid vacation/holidays/personal days, caregiver/parental and medical leave, and health benefits (medical, prescription drug, dental, vision).