Senior Project Manager - Clinical Trials

November 12

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pfm medical, inc.

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Medical Device Manufacturing

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Description

• Are you an experienced full service Project Manager in the field of clinical trials engaged in addressing the challenges facing the research and development of novel compounds in Oncology? • Passionate about impacting the health and lives of patients around the world? • Take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? • Precision for Medicine (CRO) is looking to hire a Senior Project Manager ideally with experience in Oncology & either CAR T or Radio Pharm who have managed full service clinical trials within a CRO setting to join our global team. • In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). • Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality. • Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout. • Work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team. • Join a people-focused CRO with a supportive and collaborative environment promoting work life balance and team development.

Requirements

• 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