Clinical Project Manager

I am partnered with a top Global CRO company who have an exciting opportunity for a Global Project Manager to join their Danish team.

As a full service provider, they offer a range of service to their clients. Working with them on exciting & innovative trials. With a strong research focus in oncology, metabolic, autoimmune diseases and HIV. 

My client is looking for a Senior Study Manager / Global Project Manager / Project Manager / Study Manager / Clinical Trial Manager to join their growing business in the Denmark. If you are an experienced clinical manager, please read further…

Job responsibilities:

•             Responsible for execution and delivery of assigned studies to timelines, budget and quality expectations as defined

•             Responsible for the discipline of risk-based planning, organizing and managing contingency plans for each stage of the study to bring about the successful completion of specific project in a timely manner

•             Ability to ensure the quality and integrity of studies conducted in specific countries by taking appropriate business management activities as agreed with Senior Management

•             Responsible for study oversight: coordinating internal and external operational activities, maintaining clear visibility to sites’ progress and issues and reviewing protocol deviations and metrics

•             Ability to develop and maintain regional study plan and forecasts, including budgets, milestones, timelines, quality, and risk planning

•             Ability to lead countries/sites feasibility and preparation of pre-site selection in cooperation with Medical Advisors and Regional Management.

•             Ability to drive trial start up by coordinating preparation of CPC by respective members and tracking progress of start- up milestones

•             Responsible for regional recruitment at the study level, including responsibility for forecasting and setting up contingency plans to ensure a target is achieved

Job requirements:

•             > 4+ years of clinical research experience, in planning/executing and monitoring clinical trials

•             > 4 years of experience in a regional/global project management role

•             Experience in oncology trials preferred

•             Strong project management mindset, and ability to work and lead in a matrix team environment involving both internal and external Partners

•             Excellent organizational skill

•             Ability to prioritize and work effectively in a complex matrix environment

•             Excellent leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives 

Benefits:

•             Competitive salary + bonus

•             Private Medical care

•             Life Insurance - 4x your salary (including dependents)

•             Flexible / remote working opportunities

•             Excellent Career progression & Development pathway

•             30 days holiday + bank holidays

•             Company car / car allowance