Associate Director, Clinical Sciences, Oncology

Location: Cambridge, MA or Princeton, NJ, United States; 70% in-office with up to 30% work from home. Travel up to 15% is required.

Salary: $158,600–$285,500 per year, plus potential bonus, incentive compensation, or equity.

Company

hirify.global develops mRNA-based therapeutics and vaccines across infectious diseases, immuno-oncology, rare diseases, and cardiovascular diseases.

What you will do

• Support the Clinical Study Lead in the design, execution, evaluation, and closeout of Phase 1–3 oncology clinical studies.
• Oversee study start-up, site activation, patient enrollment, protocol delivery, and operational risk reduction.
• Review and analyze clinical data, including case report forms, data listings, medical coding, and patient profiles.
• Coordinate clinical safety monitoring and support treatment discontinuation and other protocol-based safety decisions.
• Author and review protocols, informed consent documents, DSURs, Investigator Brochures, INDs, and marketing application materials.
• Prepare investigator and advisory board meetings, support inspection readiness, and contribute to clinical trial process improvements.

Requirements

• PhD, PharmD, master’s degree, or advanced nursing degree with significant scientific and clinical oncology knowledge.
• At least 8 years of clinical development experience in a pharmaceutical or biotechnology company.
• Substantial knowledge of drug development, clinical trial data integrity, data analysis, exploratory analyses, and data presentation.
• Strong written, oral, presentation, teamwork, and cross-functional collaboration skills.
• Experience with Medidata Rave and clinical data analytics platforms such as Elluminate or Spotfire is preferred.
• Must work from the Cambridge, MA or Princeton, NJ office locations and qualify as a U.S. person under U.S. export control laws; visa sponsorship is not available.

Nice to have

• Experience operating in a matrix environment and contributing to both early- and late-stage clinical development programs.
• Collaboration experience with Drug Discovery, Translational Medicine, Regulatory Affairs, Biostatistics, Medical Affairs, and Commercial functions.
• Strong scientific and clinical oncology expertise with a record of well-executed clinical research.

Culture & Benefits

• 70/30 in-office working model focused on collaboration, innovation, teamwork, and mentorship.
• Competitive healthcare and voluntary benefits.
• Fitness, mindfulness, mental health, family planning, fertility, adoption, and surrogacy support.
• Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
• Savings and investment programs, plus location-specific perks.