Director Clinical Research- Ophthalmology

Bridgeway Partners, Inc.; Los Angeles (CA); On-site; USD 130,000 - 180,000; Full time

Job summary

A leading pharmaceutical company is seeking a Director of Clinical Research to lead global clinical programs in ophthalmology. The individual will manage clinical studies from start-up to completion, ensuring alignment with regulatory requirements and effective collaboration with internal and external teams. Ideal candidates will have significant experience in clinical trials, strong leadership skills, and a proven track record in managing complex studies in ophthalmology. This role offers a unique opportunity to impact eye care therapies.

Qualifications

• Significant experience leading clinical trials in ophthalmology, preferably within the pharmaceutical or biotech sectors.
• Proven success in managing complex, multi-site clinical studies.
• Strong leadership background overseeing clinical teams and vendors.

Responsibilities

• Lead the planning and execution of clinical studies for ophthalmology therapies.
• Oversee clinical programs from study start-up through completion.
• Partner with Regulatory, R&D, and Medical Affairs departments.

Skills

Leading clinical trials in ophthalmology

Managing complex, multi-site clinical studies

Cross-functional collaboration

Strong leadership

Job description

Director, Clinical Research – Ophthalmology

We are partnering with an innovative Pharmaceutical/Biotech company developing breakthrough technologies in ophthalmology. The organization is seeking a Director of Clinical Research to lead global clinical programs supporting next-generation eye care therapies.

This leader will guide clinical strategy and execution from early feasibility through pivotal trials, working closely with internal teams and external investigators to bring new ophthalmic solutions to patients.

Key Responsibilities

• Lead the planning and execution of clinical studies for ophthalmology therapies.
• Oversee clinical programs from study start-up through completion, ensuring milestones, timelines, and budgets are achieved.
• Partner with Regulatory, R&D, and Medical Affairs to align clinical strategy with product development and regulatory requirements.
• Manage relationships with investigators, clinical sites, and external vendors.
• Provide leadership to clinical operations teams, including CRAs, project managers, and study personnel.
• Support the development of study protocols, clinical documentation, and trial reporting.
• Identify and resolve challenges related to patient enrollment, site performance, and study execution.

Qualifications

• Significant experience leading clinical trials in ophthalmology, preferably within the pharmaceutical, biotech or combination product space.
• Proven success in managing complex, multi-site clinical studies.
• Strong leadership background overseeing clinical teams and vendors.
• Experience collaborating with cross-functional partners across clinical, regulatory, and product development groups.
• Ability to work closely with investigators and key opinion leaders in the ophthalmology community.