Remote Ophthalmology Clinical Program Lead

Dompé farmaceutici S.p.A.; San Mateo, Northern (CA, KY); Hybrid; USD 161,000 - 189,000; Full time

Benefits offered by this job

Comprehensive medical benefits

Generous vacation / holiday time off

Competitive 401(K) matching

Job summary

Dompé seeks a Clinical Development Scientist, Clinical Program Lead with a strong background in life sciences and clinical research. You will collaborate with cross-functional teams to design and execute ophthalmology studies, supporting the Senior Director and ensuring quality and regulatory compliance across trials.

Responsibilities include document preparation, medical monitoring, and external interactions with vendors and advisory boards.

Qualifications

• Bachelor/advanced life sciences education with 4+ years of research experience.
• Knowledge of clinical drug development preferred but not required.
• Strong English written and spoken communication skills.
• Experience performing literature searches and using reference managers.
• Proficiency with MS Office (Word, PowerPoint, Excel) and data handling.

Responsibilities

• Assist in preparing clinical study documents (protocols, IBs, CSRs, CRFs, ICFs) in compliance with SOPs.
• Coordinate with internal stakeholders to enable timely study execution.
• Support medical monitoring and data management alongside the study team.
• Prepare and present materials for advisory boards, investigator meetings, and progress updates.
• Engage with vendors/CROs and external stakeholders to drive study deliverables.

Skills

English proficiency

MS Office

Literature searches

Scientific communication

Education

Life sciences degree

Advanced degree preferred

Tools

MS Office

Job description

Dompé seeks a Clinical Development Scientist, Clinical Program Lead with a strong background in life sciences and clinical research. You will collaborate with cross-functional teams to design and execute ophthalmology studies, supporting the Senior Director and ensuring quality and regulatory compliance across trials.

Responsibilities include document preparation, medical monitoring, and external interactions with vendors and advisory boards.