November 12
• Engage in addressing challenges facing the research and development of novel compounds in Oncology. • Passion for impacting the health and lives of patients globally. • Provide consultative approach to trial management. • Manage full service clinical trials within a CRO setting. • Full service oversight for clinical projects across clinical trials (ph I-IV). • Accountable for clinical project delivery and oversight of all functional departments. • Involved in all study stages, including proposal strategy, development, and costing. • Work with internal and external stakeholders, driving quality and coordinating the 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 working in the CRO industry is essential. • 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. • Experience managing studies within Oncology with additional experience in Radio Pharm and/or CAR T • Working understanding of GCP/ICH guidelines and the clinical development process • Ability to drive and availability for domestic and international travel including overnight stays • Be able to communicate effectively in the English language 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 with individual and teams internally and externally • Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
• Work life balance • Supportive and collaborative environment • Team development
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