Associate Medical Director

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.

Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.

THIS POSITION WILL BE LOCATED IN THE PACIFIC NORTHWEST

Position Summary :

The Associate Medical Director is a strategic medical affairs role supporting the development and lifecycle of innovative retinal therapeutics. Serves as a key medical and scientific partner to internal teams and external stakeholders, including retina specialists, investigators, and key opinion leaders (KOLs), contributing meaningfully to evidence generation, scientific exchange, and medical decision-making across the drug development continuum. Retina clinical research experts responsible for the co-development and execution of Medical Collaboration scientific strategies spanning clinical development studies (phases 1-3), post-marketing studies, and payer-informed research activities. Associate Medical Directors drive clinical trial enrollment support and strategic enrollment activities (steering committees, study coordinator committees, and investigator advisory boards) in collaboration with Clinical Operations. Associate Medical Directors participate in the development of research questions, data analysis, interpretation, presentation, and publication of Ocular Therapeutix data across Scientific Congresses and payer audiences (as needed.)

Principal Duties and Responsibilities include the following :

• Serve as a scientific expert and external-facing medical representative in the retina space, engaging with retina specialists, investigators, and KOLs


• Develop and maintain deep, long-term scientific relationships with thought leaders in retinal disease


• Lead high-level scientific discussions related to mechanism of action, clinical data, trial design, and unmet medical needs


• Act as a medical partner to Clinical Development, Regulatory, Commercial, and Market Access teams


• Translate external insights into actionable internal recommendations to inform development and lifecycle strategy


• Support internal training and education for cross-functional teams on disease state, competitive landscape, and emerging science


• Collaborate with study site principal investigators and study coordinators and Clinical Operations to execute clinical trial enrollment goal strategies (study site activation, screening, recruitment, and retention strategies/tactics.)


• Inform future clinical trial study design considerations per relevant study site insights.


• Develop and inform retrospective data generation analytic strategies (database and post hoc analyses) to address questions relevant to investigators and our Clinical Development Research Program(s)


• Support and execute Clinical Steering Committees, Study Coordinator Steering Committees, Investigator Advisory Boards, and Scientific Advisory Boards


• Support/collaborate with Medical Communications vendor partners and internal Scientific Communications colleagues on behalf data generation and publication activities.


• Identify investigator sites and deliver clinical training as needed across study sites


• Support Market Access strategies via payer-informed study design considerations across Retina Clinical Development Research Program(s) as needed.

Qualification Requirements :

• Advanced degree with 3-5+ years retina-focused background (MD, OD, PhD, PharmD etc.)
  
  
  
  • Retina clinical research/study design experience preferred.
  
  
  • 2+ years experience in Medical Affairs, Medical Science Liaison, Clinical Development, or a related pharmaceutical/biotech role
  
  


• Demonstrated analytical capabilities (data analysis, statistical concepts)


• Study enrollment experience preferred.


• Excellent verbal & written communication skills


• Strong leadership and team building


• Ability to work with and collaborate with all organization functional levels

Weekly travel to engage with retina specialists and Medical Congress attendance required.

 

 

 

Salary Range

$190,000 - $230,000 USD

Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at . For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice .