Global Study Associate Director

September 27

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TFS HealthScience

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CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting

501 - 1000

Description

• Lead a cross-functional study team and provide direction for successful study delivery. • Ensure clinical study progresses as planned, achieving milestones according to timelines and budget. • Facilitate communication across all functions and with external partners. • Manage study budget and provide budget progress reports. • Develop and maintain relevant study plans and risk management strategies.

Requirements

• University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. • 5 years of relevant clinical experience in the pharmaceutical industry, including 2 years’ project management experience, or equivalent combination of education, training and experience. • Extensive knowledge of ICH-GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development. • Demonstrated solid project management skills and knowledge of relevant tools • Strong, demonstrated abilities/skills in team leadership

Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth