March 8
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• Independently lead clinical projects within study budget and scope of work • Set and achieve objectives in project execution • Serve as primary point-of-contact liaison with clients • Handle all aspects of clinical research trials • Total project management for all functional areas • Prepare project status updates for clients and management • Contribute towards efficient management and execution of trials • Prepare and review protocols and other study documentation
• Degree or similar related life science qualification, or equivalent combination of education and experience • Previous experience in a full service/global Project Management role within a CRO • 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting • Working understanding of GCP/ICH guidelines and the clinical development process • Availability for domestic and international travel • Effective communication skills in English, both written and spoken • Strong presentation skills • Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS) • Ability to develop positive working relationships with individuals and teams internally and externally • Demonstrated core understanding of medical terminology and clinical trial activities related to the execution of a clinical development plan
• Competitive salary based on experience • Opportunity for growth and advancement within a global team • Chance to work on cutting-edge and impactful clinical trials in Oncology, Rare Diseases, and CNS • Supportive and collaborative work environment • Promotion of work-life balance and team development • High-energy, dedicated, and collaborative team members • Opportunity for domestic and international travel
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