Clinical Project Manager

il y a 5 jours

Gent, Belgique Viroclinics-DDL Temps plein

In the role of Project Manager you are the main point of contact for the client post study award. Throughout the entire lifecycle (set-up, delivery and closeout) you are responsible for leading and driving project execution. You are accountable for the initial scope management, project set-up and delivery; operational management, change management and budget management activities. Next to this you manage and collaborate with all cross-functional teams toward timely achievement of project related objectives. You develop and maintain excellent client relationships.

Project management is a key driver of Cerba's success. The different Project Teams manage and coordinate clinical trials and the development of new biotechnology. The Project Managers play an essential role in driving valuable projects to a success and bringing them successfully to market.

**Your responsibilities**:
Study set-up and planning
- Manage assigned project / client relationships, establish a core project team to support project execution throughout the set-up, delivery and closeout stages of the lifecycle
- Understand the client needs and ensure solutions are developed to meet the client needs and requirements for the project
- Align all key stakeholders on project objectives and deliverables, agree the scope, strategy and priorities
- Develop project plan with key milestones, timelines and deliverables
- Partner with the Trial set-up Manager to ensure accurate set-up and change management
- Communicate project status updates and monitor and maintain project status updates, resolve project challenges

Study delivery management and monitoring:

- Establish a study monitoring plan to ensure key endpoints for the project are being delivered
- Lead and participate in client facing meetings
- Monitor site issues and trends and administer relevant training for sites, CROs, Sponsor to ensure project compliance and successful project delivery
- Manage scope changes, work with contracts-proposals team to implement revised budgets
- Report on core project team performance or service delivery performance, report progress
- Analyze service issues and implement actions to correct and prevent issues reoccurring, lead problem solving and resolution efforts
- Travel and present lab services at client meetings, investigator meetings and BD meetings
- Provide training and mentoring to new project team members
- Participate or come up with process improvement initiatives
- Minimum of 5 years of global clinical pharmaceutical industry experience including 2 years of demonstrated skills and competency in clinical project management.
- University degree (life science or other) or equivalent combination of education and experience the provides the individual with the required knowledge, skills and abilities.
- Experience in managing global clinical trial programs.
- Sound planning, time management and organizational skills
- Demonstrated problem solving and decision-making skills
- Effective communication skills, good collaboration and interpersonal skills
- Understanding of clinical research principles and processes
- Able to prioritize own workload and manage tasks assigned to core project team members
- Cross cultural awareness and ability to adapt appropriately
- Strong presentation and influencing skills

**Working at Cerba Research**

Cerba Research is growing fast on a global scale. Working at Cerba Research first of all means that you contribute to improve global health. It also means growing your career in a dynamic, fast paced environment, where you can develop new skills and work on diverse projects. There is plenty of room for initiatives, we encourage you to take ownership, cooperate, keep learning and most and for all, have fun Working at Cerba Research also comes with its challenges and it’s not for everyone.

**Excited and ready to contribute to improve people's health on a global scale? Then please apply

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