November 12
• Lead clinical projects in accordance with budget and scope of work • Serve as primary point-of-contact liaison with clients • Liaise with project team and senior management • Handle and lead all aspects of clinical trials • Total project management for functional areas including data management, safety, clinical, medical monitoring, and biostatistics • Prepare project status updates for clients and management • 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 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
• Supportive and collaborative environment promoting work-life balance • High-energy, dedicated team members
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