Ophthalmology Clinical Development Medical Director

Astellas Pharma; Northbrook (IL); Hybrid; USD 207,000 - 296,000; Full time

Benefits offered by this job

Medical, Dental and Vision Insurance

401(k) match

Company paid life insurance

Annual Corporate Bonus

Long Term Incentive Plan

Company fleet vehicle

Referral bonus program

Job summary

Astellas Pharma in Northbrook, IL is seeking a Development Physician to drive ophthalmology clinical development plans, review safety data, and help design study documents. You will ensure regulatory alignment and provide medical leadership across trials.

The role requires collaboration with global teams, investigators, and external partners to maintain rigorous safety oversight and scientific integrity throughout program development.

Qualifications

• Medical Degree with ophthalmology residency completed.
• 8+ years in biotech/pharma drug development or equivalent academic research.
• Strong scientific writing and data analysis skills.
• Experience with safety data review and regulatory reporting.
• Proficiency with ICH/GCP guidelines and medical terminology.

Responsibilities

• Design and advance the clinical development plan aligned with asset strategy.
• Provide medical oversight and safety monitoring for trials.
• Review protocols, safety narratives, and regulatory submissions.
• Coordinate with internal/external stakeholders, including investigators.
• Lead training on safety monitoring and study oversight.

Skills

Medical Degree

Ophthalmology Residency

Clinical trial data analysis

Scientific writing

ICH/GCP knowledge

KOL/investigator engagement

Cross-functional collaboration

Regulatory affairs familiarity

Board Certification (preferred)

Education

Medical Degree with Ophthalmology residency

Job description

Astellas Pharma in Northbrook, IL is seeking a Development Physician to drive ophthalmology clinical development plans, review safety data, and help design study documents. You will ensure regulatory alignment and provide medical leadership across trials.

The role requires collaboration with global teams, investigators, and external partners to maintain rigorous safety oversight and scientific integrity throughout program development.