Director, Clinical Scientist

Scorpion Therapeutics; United States; Remote; USD 140,000 - 200,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Clinical Scientist to oversee ophthalmology product development, focusing on clinical trial design, data analysis, and regulatory documentation.

You will prepare clinical protocols, reports and submissions, manage trial data review, ensure GCP and regulatory compliance, and support site initiation and recruitment strategies, collaborating with clinical development teams and CROs for regulators and publications.

Qualifications

• PhD or PharmD in life sciences with 10+ years in clinical research.
• Expertise in ophthalmology and drug/device combination products.
• Knowledge of all clinical development phases, regulatory submissions, and GCP.

Responsibilities

• Oversee ophthalmology product development and trial design.
• Prepare clinical protocols, reports, and submissions.
• Manage trial data review and ensure GCP/regulatory compliance.
• Support site initiation and recruitment strategies.
• Collaborate with clinical development teams and CROs; prepare materials for regulators and publications.

Skills

Clinical trial design

Data analysis

Regulatory documentation

GCP compliance

Cross-functional collaboration

Education

PhD or PharmD in life sciences

Job description

Role

Senior Clinical Scientist overseeing ophthalmology product development, focusing on clinical trial design, data analysis, and regulatory documentation. Responsibilities include preparing clinical protocols, reports, and submissions, managing trial data review, ensuring compliance with GCP and regulatory standards, and supporting site initiation and recruitment strategies. Collaborates across clinical development teams and CROs, preparing materials for regulatory agencies and scientific publications.

Requirements

PhD or PharmD in life sciences; 10+ years in clinical research, especially in ophthalmology and drug/device combination products; expertise in all clinical development phases, regulatory submissions, and GCP principles.

Preferred

experience in ophthalmic therapeutics, strong scientific literature interpretation, and cross-functional teamwork skills.

HighValue

ophthalmology, drug/device combination, clinical trial phases (all), regulatory submissions, GCP compliance, global trial management.

WorkSetup

remote; no travel specified.