Senior Clinical Trial Associate (Sr. CTA) NX-1607

Scorpion Therapeutics; Brisbane (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Operations professional to manage key trial processes onsite in Brisbane, CA. The role includes TMF integrity, vendor coordination, and mentoring junior staff, with responsibilities spanning document management, quality reviews, and study material development.

You will draft plans, manuals, and patient materials, coordinate supplies, and address data reconciliation issues while representing Clinical Operations in cross-functional meetings.

Qualifications

• Bachelor's degree or equivalent required.
• 3–5+ years in Clinical Operations or clinical research.
• Proven ownership of TMF and vendor relationships.
• Strong problem-solving and communication skills.
• Proficiency in MS Office.

Responsibilities

• Develop, track, and archive essential trial documents.
• Lead TMF quality reviews and resolve discrepancies with CROs.
• Draft study plans, manuals, and patient materials.
• Coordinate clinical supplies and lab samples.
• Manage data reconciliation issues.
• Represent Clinical Operations in meetings and contribute to training materials.

Skills

TMF ownership

Vendor relationships

Problem-solving

Communication skills

MS Office

Education

Bachelor's degree or equivalent

Tools

MS Office

Job description

Role

Manage key operational aspects of clinical trials, including TMF integrity, vendor coordination, and study document management, while mentoring junior team members.

Responsibilities

• develop, track, and archive essential trial documents;
• lead TMF quality reviews and resolve discrepancies with CROs;
• independently draft study plans, manuals, and patient materials;
• coordinate clinical supplies and lab samples;
• manage data reconciliation issues;
• represent Clinical Operations in meetings and contribute to training material development.

Requirements

• Bachelor's degree or equivalent;
• 3–5+ years in Clinical Operations or clinical research;
• proven ownership of TMF and vendor relationships;
• strong problem-solving and communication skills;
• proficiency in MS Office.

Preferred qualifications

Preferred qualifications are not specified.

High-Value

role involves CRO/vendor oversight, study document management, and operational problem resolution within a biopharma clinical trial setting.

Location

onsite in Brisbane, CA.