Senior Clinical Development Scientist

Scorpion Therapeutics; California (MO); On-site; USD 90,000 - 150,000; Full time

Job summary

Scorpion Therapeutics is seeking a supportive clinical research associate to contribute to late-stage oncology trials, with a focus on CAR-T therapies. You will collaborate with Clinical Scientist Program Lead and cross-functional teams to shape trial design, develop protocols, and ensure high-quality study documentation across multiple phases.

This role emphasizes data analysis, regulatory submissions, and trial start-up to close-out activities, with potential for clinical monitoring.

Qualifications

• PharmD or PhD in clinical research or pharmacology with industry experience.
• MS with 6+ years in drug development.
• BS or RN with 8+ years in drug development, preferably in MM or CAR-T.
• Experience in oncology or cell therapies is preferred.

Responsibilities

• Collaborate on trial design and protocol development.
• Develop protocols and study documents.
• Assist in data analysis and reporting.
• Contribute to regulatory submissions.
• Support trial start-up, execution, and close-out activities with potential for clinical monitoring.

Skills

Regulatory submissions experience

Cross-functional collaboration

Clinical trial design knowledge

Travel willingness

Education

PharmD or PhD in clinical research or pharmacology

MS with 6+ years

BS or RN with 8+ years in drug development

Tools

Clinical data systems

Job description

Role

Supportive clinical research associate in late-stage oncology trials, focusing on CAR T-cell therapies for cancer.

Responsibilities

• collaborate on trial design
• develop protocols and study documents
• assist in data analysis and reporting
• contribute to regulatory submissions
• support trial start-up, execution, and close-out activities, with potential for clinical monitoring.

Requirements

• PharmD or PhD in clinical research or pharmacology with relevant industry experience
• MS with 6+years
• BS or RNwith8+years in drug development, preferablyinMultiple Myeloma or CAR‑T therapy

Knowledge

Knowledge of clinical trial design and regulatory guidelines (FDA…;EMA…GCP ).…

Preferred

• experience in oncology, immunotherapies, or cell therapies
• proficiency with clinical data systems
• ability to adapt to new therapeutic areas
• strong communication skills
• ability to travel as needed

Collaboration

work closely with Clinical Scientist Program Lead and cross-functional teams within a late-stage oncology development setting.

Work Setup

not specified, but involvement in multiple phases suggests a flexible, regulated environment.