Associate, Study Management III - Remote

Overview

The Associate, Study Management III will be part of a dynamic, centralized study management team that is responsible for the execution of global clinical trials. This role involves working independently and collaboratively to ensure studies are executed with quality and efficiency, aligning with the company’s strategic objectives.

In Short

• Lead and manage one or more global clinical trials.
• Work independently as a clinical study leader.
• Support the Study Project Manager in strategic leadership.
• Manage vendor relationships and oversee deliverables.
• Develop and execute recruitment strategies for clinical trials.
• Ensure compliance with quality standards and regulations.
• Co-develop and manage study materials.
• Provide training to stakeholders as needed.
• Participate in risk management and issue resolution.
• Ensure inspection readiness for audits.

Requirements

• Bachelor’s Degree or equivalent required.
• At least 4 years of experience in Pharma or clinical research.
• Competence in ICH/GCP and Global Regulations.
• Experience with EDC, IRT, CTMS, and eTMF systems.
• Strong analytical and critical thinking skills.
• Excellent organizational and time management skills.
• Exceptional interpersonal and communication skills.
• Proactive and collaborative mindset.
• Able to work independently in a global team environment.
• Preferred: Experience with global study exposure.

Benefits

• Comprehensive benefits package including medical, dental, and vision insurance.
• Paid time off including vacation and holidays.
• Participation in short-term incentive programs.
• Opportunities for professional development.
• Supportive work environment promoting work-life balance.