Remote Associate Director, Ophthalmology Clinical Scientist

Initial Therapeutics, Inc.; Oregon (WI); Hybrid; USD 154,500 - 249,947; Full time

Job summary

Initial Therapeutics, Inc. is seeking an Associate Director in Clinical Development to lead the implementation of Clinical Development Plans. This remote role requires significant experience in clinical drug development and a strong grasp of Good Clinical Practice (GCP).

The successful candidate will collaborate with cross‑functional teams to ensure compliance with health authorities and participate in all phases of clinical research including regulatory submissions. A PhD or PharmD is required.

Qualifications

• A complete understanding and application of clinical research procedures and GCP.
• Minimum of 5+ years of clinical development/research and R&D experience preferred for Associate Director Level.
• Experience with all phases of clinical drug development including regulatory submissions.

Responsibilities

• Contribute to Clinical Development Plans and Registrational Strategies.
• Collaborate with Clinical Research Organizations on clinical trial documents.
• Assist in management of clinical trial data collection and analysis.
• Ensure compliance with regulatory authority guidelines for clinical trials.
• Assist with clinical documents for submission to global health authorities.

Skills

Clinical research procedures and Good Clinical Practice (GCP)

Experience in ophthalmology

Strong communication skills

Organizational skills

Interpersonal skills

Independent decision-making skills

Analytical skills

Experience in matrix team environments

Education

Advanced degree in life science/clinical/medical field, PhD or PharmD

Job description

Initial Therapeutics, Inc. is seeking an Associate Director in Clinical Development to lead the implementation of Clinical Development Plans. This remote role requires significant experience in clinical drug development and a strong grasp of Good Clinical Practice (GCP).

The successful candidate will collaborate with cross‑functional teams to ensure compliance with health authorities and participate in all phases of clinical research including regulatory submissions. A PhD or PharmD is required.