November 12
• Responsible for full service oversight of clinical projects across global/regional trials • Manage clinical project delivery ensuring timelines, scope, cost and quality are met • Oversee all functional departments involved in trial management • Lead the project through all study stages, including proposal strategy and development • Serve as primary point-of-contact with clients, providing excellent customer service • Liaise with internal and external stakeholders to drive quality and coordination of study team
• 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 the CRO industry is essential. • 5 to 7 years industry experience, with at least 3 years in full service Project Management in a clinical trial setting within a Clinical Research Organisation. • Experience managing studies in Oncology, with additional experience in Radio Pharm and/or CAR T • Working understanding of GCP/ICH guidelines and clinical development process • Ability to drive and availability for domestic and international travel including overnight stays • 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) • Proven ability to develop positive working relationships internally and externally • Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
• Supportive and collaborative environment promoting work-life balance • Opportunities for team development • High-energy, dedicated team
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