Clinical Scientist/ Senior Clinical Scientist

Scorpion Therapeutics; South San Francisco (CA); On-site; USD 180,000 - 230,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Clinical Development Scientist to lead oncology, dermatology, or autoimmune disease trials. You will drive protocol development, regulatory document preparation, and clinical trial oversight, partnering with cross-functional teams.

The role requires a PhD, PharmD, RN, NP, or PA with 5+ years of biotech experience. Travel to field sites and scientific meetings may be required as part of clinical operations.

Qualifications

• Requires PhD, PharmD, RN, NP or PA and 5+ years biotech experience in oncology, dermatology, or autoimmune areas.
• Experience leading protocol development and regulatory document preparation.
• Strong medical monitoring and cross-functional collaboration skills.

Responsibilities

• Contribute to clinical plans and protocols; support regulatory document creation (Investigator Brochures, DSURs).
• Assist in trial implementation, review clinical data, and participate in medical monitoring activities.
• May lead activities of other team members and coordinate cross-functional efforts.

Skills

Clinical development

Leadership

Regulatory documents

Medical monitoring

Education

PhD/PharmD/RN/NP/PA

Job description

Role

Senior Clinical Development Scientist supporting oncology, dermatology, or autoimmune disease trials with leadership in protocol development, regulatory document preparation, and clinical trial oversight.

Responsibilities

contribute to clinical plans and protocols, assist in regulatory document creation (e.g., Investigator Brochures, DSURs), support trial implementation, review clinical data, and participate in medical monitoring activities. May lead activities of other team members and coordinate cross-functional efforts.

Requirements

PhD, PharmD, RN, Nurse Practitioner, or Physician Assistant; 5+ years biotech experience in relevant therapeutic areas.

High-Value

biotech industry, oncology/autoimmune/dermatology focus, clinical trial conduct, protocol writing, regulatory document development, medical monitoring.

Collaboration

works closely with Data Management and clinical teams; may coordinate team activities.

Work Setup

not specified; travel to field sites and scientific meetings may be required.