Associate Director, Study Manager, Immunology

Scorpion Therapeutics; Rahway (NJ); Hybrid; USD 170,000 - 210,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Trial Lead to oversee the operational planning and execution of clinical trials within the program, serving as the Clinical Trial Team lead. You will manage trial feasibility, stakeholder collaboration, and governance, while guiding study planning and issue resolution.

The role includes reviewing clinical documents and developing team capabilities through coaching, with potential direct reports.

Qualifications

• Minimum 9+ years in pharma/clinical development with a Bachelor's degree or 6+ years with an advanced degree.
• Strong knowledge of GCP and ICH regulations.
• Proven leadership and cross-functional collaboration skills.

Responsibilities

• Manage trial feasibility, conduct, and stakeholder collaboration.
• Lead study planning, issue resolution, and governance.
• Review clinical documents and build team capabilities through coaching and mentoring (potentially including direct reports).

Skills

Leadership & collaboration

GCP/ICH knowledge

Pharma/clinical development

Education

Bachelor's degree + 9+ yrs

Advanced degree + 6+ yrs

Job description

Role:

Lead and oversee the operational planning and execution of clinical trials within the Tulisokibart program, serving as the Clinical Trial Team lead.

Responsibilities:

manage trial feasibility, conduct, and stakeholder collaboration; lead study planning, issue resolution, and governance; review clinical documents, and build team capabilities through coaching and mentoring, potentially including direct reports.

Requirements:

Bachelor's degree with 9+ years or advanced degrees with 6+ years in pharmaceutical/clinical development, project management, or medical fields; strong knowledge of GCP and ICH regulations; proven leadership and cross-functional collaboration skills.

HighValue:

experience in global clinical trials, particularly in immunology, autoimmune, or immune-mediated disorders; familiarity with clinical trial phases from initiation through database lock; expertise in clinical operations and vendor management.

Work Setup:

hybrid, with approximately 10% travel.