Associate Director, Clinical Scientist - Ophthalmology
EyePoint
August 13, 2026
Remote
United States
Clinical Research and Development
Responsibilities:
- Collaborate with cross-functional teams to implement Clinical Development Plans and Registrational Strategies for assigned products.
- Work with Clinical Development teams and partnered CROs on clinical trial documents (protocol synopses/protocols, investigator brochures, informed consent templates, case report forms/EDC, procedure manuals, clinical study reports) in compliance with ICH/GCP, federal/local regulations, and company SOPs.
- Assist with collection, review, and analysis of clinical trial data per interim and overall statistical analysis plans.
- Perform ongoing active review of clinical data for trends in safety, effectiveness, and protocol adherence.
- Assist in preparing submission documents for global health authorities (e.g., EMA Scientific Advice, Pre-IND, IND, End-of-Phase II, NDAs, MAAs, and other regulatory meetings/filings).
- Support authorship of meeting abstracts/posters and publication of trial data per the program’s publication strategy.
- Assist with site initiation activities (site initiation visits, investigator meetings, monitoring plan development/implementation, annotated monitoring visit templates; ensure required documents are completed/submitted prior to initiation).
- Assist with clinical trial recruitment strategies (track enrollment vs. targets and support sites to meet/exceed targets with Clinical Operations).
- Support study milestones and metrics with Clinical Operations.
- Ensure global clinical trial conduct aligns with global regulatory requirements, ICH, and GCP.
Primary skills/knowledge required:
- Strong understanding and application of clinical research procedures and GCP.
- Ophthalmology experience; familiarity with drug/device combination products.
- Experience across all phases of clinical drug development, including regulatory submissions.
- Ability to survey and interpret scientific literature related to the product portfolio.
- Strong communication, organizational, and interpersonal skills.
- Experience working in matrix environments with cross-functional teams.
- Independent decision-making and analytical skills.
Education:
- Advanced degree in life science/clinical/medical field (PhD or PharmD).
Experience:
- Minimum 5+ years in clinical development/research and R&D (preferred for Associate Director level).
Pay range:
- $154,500 USD - $195,700 USD
- Collaborate with cross-functional teams to implement Clinical Development Plans and Registrational Strategies for assigned products.
- Work with Clinical Development teams and partnered CROs on clinical trial documents (protocol synopses/protocols, investigator brochures, informed consent templates, case report forms/EDC, procedure manuals, clinical study reports) in compliance with ICH/GCP, federal/local regulations, and company SOPs.
- Assist with collection, review, and analysis of clinical trial data per interim and overall statistical analysis plans.
- Perform ongoing active review of clinical data for trends in safety, effectiveness, and protocol adherence.
- Assist in preparing submission documents for global health authorities (e.g., EMA Scientific Advice, Pre-IND, IND, End-of-Phase II, NDAs, MAAs, and other regulatory meetings/filings).
- Support authorship of meeting abstracts/posters and publication of trial data per the program’s publication strategy.
- Assist with site initiation activities (site initiation visits, investigator meetings, monitoring plan development/implementation, annotated monitoring visit templates; ensure required documents are completed/submitted prior to initiation).
- Assist with clinical trial recruitment strategies (track enrollment vs. targets and support sites to meet/exceed targets with Clinical Operations).
- Support study milestones and metrics with Clinical Operations.
- Ensure global clinical trial conduct aligns with global regulatory requirements, ICH, and GCP.
Primary skills/knowledge required:
- Strong understanding and application of clinical research procedures and GCP.
- Ophthalmology experience; familiarity with drug/device combination products.
- Experience across all phases of clinical drug development, including regulatory submissions.
- Ability to survey and interpret scientific literature related to the product portfolio.
- Strong communication, organizational, and interpersonal skills.
- Experience working in matrix environments with cross-functional teams.
- Independent decision-making and analytical skills.
Education:
- Advanced degree in life science/clinical/medical field (PhD or PharmD).
Experience:
- Minimum 5+ years in clinical development/research and R&D (preferred for Associate Director level).
Pay range:
- $154,500 USD - $195,700 USD