Clinical Project Manager - Germany job in Berlin, Germany

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First Name*

Last Name*

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Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Project/Study Manager (CSM/CPM)

Location: Germany

This vacancy has now expired. Please see similar roles below...

Proclinical has partnered with an established CRO who are looking for a Clinical Project Manager to join their growing team. They are running several phase II/III studies.

You will be responsible for overseeing global studies where you will manage also manage vendors. There is a lot of opportunity to take on a range of responsibilities whilst working in an autonomous and driven environment.

This is a great opportunity to move into a truly global role and to join a company several high-profile studies ongoing.

Job Responsibilities

Takes full leadership on all project deliverables on projects assigned as gPM
Ensures that project deliveries are on time, within budget and with quality
Proactively identifies areas for process improvement and provides suggestions on process changes
Builds and manages the study budget, implement actions to mitigate areas of risk, drive delivery
across the full project, collaborate with internal stakeholders to track study progress and create study tools
Coordinates and manages project start-up, project maintenance, and project close-out activities
Effectively drives client and internal team communication
Provides leadership to KCR study team members as well as relevant vendors
Proactively and effectively communicates with assigned team members across relevant functions in order to drive project success; aims to be instrumental in the management of the client via close collaboration, both in person and remotely
Sets up all relevant study plans and keeps them updated throughout the study execution
Communicates updates to project scope and/or timelines to all parties involved
Leads teleconferences and meetings with Sponsor, Services Providers and Managers from other departments
Takes ownership of project issues and proactively drives to resolution, including relevant escalation as needed
Follows applicable SOPs and regulations and drive team compliance
Maintains study status tracking tools up to date and drives team member's compliance
Prepares reports on the assigned activities according to the requirements and timelines established by supervisor
Proactively communicates project status, issues & risks to stakeholders and management
Reviews clinical trip reports
Coordinates work of Services Providers, transparently communicating to the Sponsor all decisions and deviations related to service providers

Skills and Requirements

University/college degree (life science or medical degree preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Significant experience in project management of clinical trials (minimum 1 year of Project Management experience)
Previous or current CRO/sponsor experience or Medical Device Manufacturer experience
Broad knowledge of medical terminology, clinical patient management and clinical research
methodology
Advanced team leadership skills
Advanced decision-making skills
Demonstrates sound judgment in decision making process and has strong understanding of scope of contracts, including milestones and recognition of changes

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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