Director, Clinical Scientist
EyePoint
August 23, 2026
Remote
United States
Clinical Research and Development
Remote. This position reports to the Chief Medical Officer.
Primary Responsibilities:
- Contribute with a cross-functional team to implement Clinical Development Plans and Registrational Strategies for assigned products.
- Collaborate with Clinical Development and partnered CROs to develop and review clinical trial documents (protocol synopses/protocols, investigator brochures, informed consent templates, CRFs/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 statistical analysis plans.
- Perform ongoing review of clinical data for trends in safety, effectiveness, and protocol adherence.
- Support preparation of clinical documents for global health authority submissions (EMA Scientific Advice, Pre-IND, IND, End-of-Phase II, NDAs, MAAs, and other regulatory meetings/filings).
- Assist with authorship of abstracts/posters and publication of clinical trial data per the publication strategy.
- Support site initiation activities (site initiation visits, investigator meetings, monitoring plans, annotated monitoring visit report templates, and completion/submission of required documents prior to site initiation).
- Support clinical trial recruitment strategies; track enrollment vs. targets and work with sites/clinical operations to meet or exceed targets.
- Assist with study milestones and study metrics with clinical operations.
- Ensure proper global trial conduct in compliance with global regulations, ICH, and GCP.
Primary Skills & Knowledge (Required):
- Strong understanding/application of clinical research procedures and GCP.
- Ophthalmology experience and familiarity with drug/device combination products.
- Experience across all phases of clinical drug development including regulatory submissions.
- Ability to survey and interpret scientific literature for assigned products.
- Strong communication, organizational, and interpersonal skills.
- Experience working in matrix, cross-functional teams.
- Independent decision-making and analytical skills.
Level of Education:
- Advanced degree in life science/clinical/medical field (PhD or PharmD).
Experience:
- Minimum 10 years of clinical development/research and R&D experience preferred.
Salary Range (target):
- $197,760 USD - $249,947 USD
Primary Responsibilities:
- Contribute with a cross-functional team to implement Clinical Development Plans and Registrational Strategies for assigned products.
- Collaborate with Clinical Development and partnered CROs to develop and review clinical trial documents (protocol synopses/protocols, investigator brochures, informed consent templates, CRFs/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 statistical analysis plans.
- Perform ongoing review of clinical data for trends in safety, effectiveness, and protocol adherence.
- Support preparation of clinical documents for global health authority submissions (EMA Scientific Advice, Pre-IND, IND, End-of-Phase II, NDAs, MAAs, and other regulatory meetings/filings).
- Assist with authorship of abstracts/posters and publication of clinical trial data per the publication strategy.
- Support site initiation activities (site initiation visits, investigator meetings, monitoring plans, annotated monitoring visit report templates, and completion/submission of required documents prior to site initiation).
- Support clinical trial recruitment strategies; track enrollment vs. targets and work with sites/clinical operations to meet or exceed targets.
- Assist with study milestones and study metrics with clinical operations.
- Ensure proper global trial conduct in compliance with global regulations, ICH, and GCP.
Primary Skills & Knowledge (Required):
- Strong understanding/application of clinical research procedures and GCP.
- Ophthalmology experience and familiarity with drug/device combination products.
- Experience across all phases of clinical drug development including regulatory submissions.
- Ability to survey and interpret scientific literature for assigned products.
- Strong communication, organizational, and interpersonal skills.
- Experience working in matrix, cross-functional teams.
- Independent decision-making and analytical skills.
Level of Education:
- Advanced degree in life science/clinical/medical field (PhD or PharmD).
Experience:
- Minimum 10 years of clinical development/research and R&D experience preferred.
Salary Range (target):
- $197,760 USD - $249,947 USD