Clinical Project Manager - Germany

£60000 - £65000 per annum
  1. Permanent
  2. Project/Study Manager (CSM/CPM)
  3. Germany
Berlin, Germany
Posting date: 05 Mar 2021

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.