Study Management Associate III - Remote

Overview

As a Study Management Associate III, you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team.

In Short

• Work independently as a clinical study leader and contributor.
• Oversee global trials in a cross-functional environment.
• Support the Study Project Manager in strategic leadership.
• Manage vendor relationships and recruitment strategies.
• Lead assigned meetings and provide regular updates on study status.
• Ensure inspection readiness and participate in related activities.
• Co-develop and manage study materials and documentation.
• Engage in training for stakeholders as needed.
• Support process improvement initiatives.

Requirements

• Bachelor’s Degree or equivalent required.
• At least 4 years of Pharma-related/clinical research experience.
• Competent in standard quality procedures (SOP, ICH/GCP).
• Experienced user of 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.
• Ability to work independently in a fast-paced environment.

Benefits

• Comprehensive package of benefits including paid time off.
• Medical/dental/vision insurance.
• 401(k) for eligible employees.
• Short-term incentive programs eligibility.