Senior Clinical Research Associate

Scorpion Therapeutics; United States; Remote; USD 90,000 - 140,000; Full time

Job summary

Scorpion Therapeutics is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial operations for cell therapy programs, including tumor infiltrating lymphocyte (TIL) therapies, with a focus on solid tumors.

You will manage study start-up, conduct on-site monitoring visits, oversee CROs and labs, ensure protocol and GCP compliance, review monitoring metrics, and mentor junior staff while collaborating cross-functionally with study teams, medical monitors, and vendors.

Qualifications

• BS/BA, RN, or equivalent with 8+ years in clinical operations.
• Strong knowledge of GCP/ICH, trial management, and vendor oversight.
• Excellent communication and organizational skills; proficient with MS Office and Project.

Responsibilities

• Manage study start-up and oversee on-site monitoring visits.
• Oversee vendor relationships (CROs, labs) and ensure protocol/GCP compliance.
• Review monitoring metrics and support study documentation.
• Mentor junior staff and collaborate with study teams, medical monitors, and vendors.

Skills

GCP/ICH knowledge

Clinical trial operations

Vendor oversight

Communication skills

Organizational skills

MS Office

Project

Education

BS/BA, RN, or equivalent

Tools

MS Office

Project

Job description

Senior Clinical Research Associate (CRA) overseeing clinical trial operations for cell therapy programs, including tumor infiltrating lymphocyte (TIL) therapies, with a focus on solid tumors.

Responsibilities

• manage study start-up
• conduct on-site monitoring visits
• oversee vendor relationships (CROs, labs)
• ensure protocol and GCP compliance
• review monitoring metrics
• support study documentation
• Mentors junior staff and collaborates cross-functionally with study teams, medical monitors, and vendors.

Requirements

• BS/BA, RN, or equivalent plus 8+ years in clinical operations with experience in solid tumor or cell therapy trials
• strong knowledge of GCP/ICH, clinical trial management, and vendor oversight
• excellent communication, organizational, and computer skills (MS Office, Project)

High-Value

• High-Value: biologics/cell therapy, solid tumor indications, early to late phase (including late phase), vendor management, GCP compliance, global and multi-center trials.

WorkSetup

remote with up to 25% travel.