Associate Director, Clinical Scientist, Ophthalmology

Location: Tarrytown, NY; Warren, NJ; or Cambridge, MA. Many roles are required to be performed onsite.

Salary: $176,100–$287,300 annually

Company

hirify.global is a biotechnology company that discovers, develops, and commercializes medicines for serious diseases, including ophthalmic, inflammatory, oncological, cardiovascular, neurological, infectious, and rare diseases.

What you will do

• Serve as Clinical Scientist for ophthalmology programs or as a delegate of the therapeutic-area Clinical Scientist.
• Contribute to program meetings, scientific advisory boards, study steering committees, data and safety monitoring meetings, and cross-functional collaborations.
• Propose, design, and execute early- and late-stage clinical research and development studies.
• Develop expanded synopses and author or review protocols, amendments, medical monitoring plans, statistical analysis plans, informed consents, clinical study reports, and regulatory documents.
• Prepare and present information for investigators, governance groups, data monitoring committees, regulatory authorities, and internal collaborators.
• Review clinical data, assess risks, develop mitigation strategies, and promote consistent medical and clinical data-review practices across studies.

Requirements

• Advanced degree or equivalent education in life sciences or healthcare, such as a PhD, PharmD, or MSc.
• 10 years of pharmaceutical clinical drug development experience, including basic knowledge of ophthalmology.
• Proficient knowledge of drug development, Good Clinical Practice, study design, and clinical research methodology.
• Solid medical writing skills and experience authoring and reviewing clinical and regulatory documents.
• Experience conducting global clinical trials and executing clinical programs.
• Strong teamwork, professional diplomacy, communication, and influencing skills across internal and external functions.

Culture & Benefits

• Science-driven environment focused on developing medicines for patients with serious diseases.
• Cross-functional collaboration with internal teams, external vendors, investigators, and regulatory stakeholders.
• Benefits may include annual bonuses or incentive plans, equity awards, retirement benefits, 401(k) matching, health and wellness programs, insurance, paid time off, and family support benefits.
• Reasonable accommodation is available during recruitment for applicants with known disabilities or chronic illnesses where required.