Precision Medicine Group is hiring a
Project Manager/Senior Project Manager in Worldwide

Summary

The job is for an experienced Project Manager with a focus on Oncology, Rare Diseases or CRO setting. The role involves overseeing clinical projects across global/regional trials, managing client relationships, project team, and budget and timelines. The company offers a supportive and collaborative environment that promotes work life balance and encourages 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
• 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

Responsibilities

• 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