Precision Medicine Group is hiring a
Senior Project Manager

Summary

Join Precision for Medicine as a Senior Project Manager to lead clinical projects in Oncology, Rare Disease or CNS, and impact the health and lives of patients worldwide.

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

• Independently lead clinical projects in accordance with the study budget and scope of work
• Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
• Liaise with Project Team and senior management of both Precision and sponsors, including C level
• Handle and lead all aspects of a clinical research trial or trials
• Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc
• Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
• Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets