Senior Project Manager - Clinical Trials
November 12
Description
• Manage full service oversight for clinical projects in global/regional (ph I-IV) trials. • Accountable for clinical project delivery, oversight of all functional departments, ensuring timelines, scope, cost and quality. • Involved in all study stages, including proposal strategy, development, costing, and bid defense. • Serving as primary point-of-contact liaison with clients for excellent customer service. • Handle and lead all aspects of clinical trials including data management and safety.
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.
Benefits
• People-focused environment promoting work-life balance and team development. • High-energy, dedicated, collaborative team members.
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