Ophthalmology Clinical Development Lead

Dompé; San Mateo (CA); On-site; USD 161,000 - 189,000; Full time

Benefits offered by this job

Medical benefits

Vacation time

401(k) matching

Job summary

Dompé in the United States is seeking a Clinical Development Scientist to join the Ophthalmology team. You will partner with cross-functional colleagues to design and execute clinical studies, support medical monitoring, and prepare study documents while ensuring adherence to GCP and SOPs.

You will work with vendors and CROs, present at advisory boards, and help keep timelines on track. Travel up to 20% domestically and globally as needed.

Qualifications

• Life sciences degree or equivalent with 4 years’ research experience.
• Advanced degree in life sciences preferred but not required.
• Clinical drug development experience preferred but not required.
• General knowledge in clinical research methodology (GCP) and regulations.

Responsibilities

• Assist in preparing clinical study documents (protocols, IBs, CSRs, CRFs, ICFs, presentations) in line with SOPs.
• Coordinate with internal stakeholders to facilitate efficient study execution.
• Support monitoring under supervision and with pharmacovigilance teams.
• Assist in building CRFs and data management activities.
• Prepare presentations for scientific advisory boards and investigator meetings.
• Engage with vendors/CROs for external activities and ensure timely deliverables.
• Stay informed on therapeutic landscape and translate into development strategy.

Skills

English proficiency

Communication skills

Independent work

Cross-functional collaboration

Education

Bachelor's degree in life sciences

Advanced life sciences degree

Tools

MS Office

Job description

Dompé in the United States is seeking a Clinical Development Scientist to join the Ophthalmology team. You will partner with cross-functional colleagues to design and execute clinical studies, support medical monitoring, and prepare study documents while ensuring adherence to GCP and SOPs.

You will work with vendors and CROs, present at advisory boards, and help keep timelines on track. Travel up to 20% domestically and globally as needed.