Senior Clinical Project Manager - Oncology

The role

The Senior Clinical Project Manager provides full service oversight for global or regional oncology clinical trials from phase I to IV. This role involves managing project delivery, functional departments, timelines, scope, cost, and quality throughout the full study cycle.

What you will do

• Independently lead clinical projects in accordance with study budget and scope of work.
• Serve as the primary point-of-contact liaison with the client.
• Liaise with Project Team and senior management of Precision and sponsors.
• Handle and lead all aspects of a clinical research trial or trials.
• Provide total project management for functional areas including data management, safety, clinical, medical monitoring and biostatistics.
• Prepare project status updates for clients and management.
• Serve as an active member of the Project Team.
• Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.

Required qualifications

• 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.
• Extensive experience working within Clinical Operations position within a CRO.
• At least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
• Experience managing studies within Oncology.
• 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.

Benefits

• Supportive and collaborative environment which promotes work life balance.
• Encourages team development.

Before you apply

• Candidates must be legally authorized to work in the country of employment without employer sponsorship.

About the company

Precision for Medicine is a people focussed CRO with a supportive and collaborative environment. Their integrated offering combines clinical trial designs, operational and medical authorities, and biomarker and data analytics solutions.