Clinical Development Medical Director (MD required)

Location: United States – New York – Pearl River. Hybrid role requiring residence within commuting distance and on-site work an average of 2.5 days per week. Standard East Coast workday hours are required, with occasional off-hours work and travel.

Annual base salary: $239,900–$399,800, plus a 25% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a pharmaceutical company developing medicines through clinical research, regulatory programs, and clinical trials.

What you will do

• Provide medical and scientific oversight for one or more clinical studies, maintaining patient safety, quality, compliance, and timely delivery.
• Review individual and cumulative safety data, assess adverse events, support benefit-risk evaluations, and communicate safety information to study sites.
• Design clinical studies and contribute medical input to clinical development plans, protocols, informed consent documents, monitoring guidelines, and statistical analysis plans.
• Interpret clinical efficacy and safety data and oversee the quality of top-line analyses, clinical study reports, and public disclosures.
• Train study teams and investigators, monitor protocol and regulatory compliance, and support issue resolution, audits, inspections, and study closeout.
• Author clinical sections of regulatory documents and interact with regulatory authorities, Data Monitoring Committees, steering committees, key opinion leaders, and principal investigators.

Requirements

• Medical degree (M.D., D.O., or equivalent) is required.
• Permanent U.S. work authorization and authorization to work in the U.S. for any employer are required.
• U.S. work visa sponsorship is not available now or in the future.
• At least 4 years of work experience, including documented pharmaceutical industry experience in clinical research programs and registration activities.
• Independent medical license to prescribe medicines for at least two years after internship or houseman training, with at least one year of patient-care prescribing experience.
• Experience with clinical program and study design, clinical trial execution, critical evaluation of medical and scientific information, and management of multiple studies.

Nice to have

• Knowledge or work experience in statistics.
• Training or hospital experience in infectious diseases or infection control.
• Experience with investigational clinical trials.
• Leadership experience involving collaboration, coaching, influence, and oversight of colleagues.

Culture & Benefits

• Hybrid work arrangement with an average of 2.5 on-site days per week.
• Medical, prescription drug, dental, and vision coverage.
• 401(k) plan with company matching contributions and an additional retirement savings contribution.
• Paid vacation, holidays, personal days, caregiver or parental leave, and medical leave.
• Eligibility for performance-based bonuses and a share-based long-term incentive program.