Sr. Manager Clinical Scientist (Oncology)

Location: Remote, Woburn, Massachusetts, United States; approximately 25% work-related travel is required.

Base pay: $159,000–$205,500 per year, plus potential performance incentive bonus and equity.

Company

hirify.global is a biotechnology company developing oncolytic immunotherapies based on its RPx platform to activate systemic anti-tumor immune responses.

What you will do

• Facilitate the creation, review, and maintenance of clinical and regulatory documents, including protocols, informed consents, investigator brochures, clinical study reports, manuscripts, and clinical sections of regulatory submissions.
• Support the design, implementation, conduct, analysis, interpretation, and documentation of clinical studies.
• Provide clinical and scientific expertise for investigator, site, and vendor selection, and train internal colleagues, CRO staff, and study site personnel.
• Review and analyze clinical trial data, respond to clinical questions, and partner with the Medical Director on medical monitoring, patient eligibility, and treatment-related decisions.
• Present clinical trial data and prepare study- and program-related slide decks for internal and external audiences.
• Build investigator and KOL networks, support advisory boards and investigator meetings, and contribute to therapeutic-area research and competitor analysis.

Requirements

• Bachelor’s degree required; an advanced degree such as PharmD, PhD, or MD is preferred.
• At least 3 years of relevant experience in biotechnology or pharmaceutical companies, including 1–2 years in oncology.
• Previous participation in an early- or late-phase clinical development program is essential; clinical oncology experience is required for late-phase work.
• Knowledge of GCP and ICH Guidelines, clinical development IT solutions, and clinical study documentation is required.
• Strong written and verbal communication, organization, problem-solving, risk-mitigation, and cross-functional collaboration skills.
• Ability to work independently, manage multiple projects in a fast-paced environment, and collaborate with colleagues in a global setting.

Nice to have

• Experience working in a global cross-functional environment.
• Experience developing and supporting SOPs and related policies.
• Advanced clinical oncology experience, particularly in early-phase development.

Culture & Benefits

• Remote work arrangement with approximately 25% work-related travel.
• Medical, dental, and vision insurance.
• 401(k) matching, flexible time off, and paid holidays including a year-end shutdown.
• Annual performance incentive bonus and new-hire and ongoing performance-based equity.
• Collaborative, candid, dedicated, and scientifically focused working environment.