Associate Director, Clinical Study Management, EMEA/LATAM

Scorpion Therapeutics; Jersey City (NJ); Hybrid; USD 180,000 - 270,000; Full time

Job summary

Scorpion Therapeutics seeks an Associate Director of Clinical Study Management to lead global oncology trials (Phase I–IV) across EMEA/LATAM, ensuring regulatory compliance and operational excellence.

You will oversee regional vendors, coordinate study documentation, and manage budgets while developing regional clinical operations staff. Hybrid onsite work is required, with travel as needed.

Qualifications

• 10+ years of clinical trial management experience or 8+ years with postgraduate degree.
• Deep knowledge of GCP and regional regulations (EMEA/LATAM preferred).
• Strong leadership, communication, and organizational skills.

Responsibilities

• Lead multi-center Phase I–IV trials with oncology focus.
• Oversee regional vendors and internal resources to ensure timelines and budget adherence.
• Coordinate study documentation and regulatory submissions.

Skills

Leadership

Vendor management

Clinical study management

Regulatory compliance

ICH-GCP knowledge

Communication

Budget oversight

Education

Postgraduate degree

Tools

CTMS

EDC

Regulatory systems

Job description

Role: Associate Director, Clinical Study Management (EMEA/LATAM), overseeing global clinical trials primarily in oncology, with a focus on operational excellence, regulatory compliance, and team leadership.

Responsibilities: lead multi-center Phase I–IV trials, manage regional vendors and internal resources, ensure adherence to ICH-GCP, EMEA, and LATAM regulations, coordinate study documentation, and oversee regional budgets and KPIs; hire and develop regional clinical operations staff; provide regular stakeholder updates and contribute to process improvements.

Requirements: 10+ years of clinical trial management experience (or 8+ years with postgraduate degree), deep knowledge of GCP, regional regulations, and experience managing global trials; strong leadership, communication, and organizational skills; fluency in English, with additional EMEA/LATAM languages a plus.

HighValue: global multi‑center trials, oncology, Phase I–IV, regional regulatory expertise, vendor management, team leadership in clinical operations, working onsite 3+ days/week in Jersey City or Millbrae.

WorkSetup: hybrid onsite; travel as needed.