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MSD Associate Clinical Research Manager 
Denmark, Capital Region of Denmark 
651911858

28.07.2024

Job Description

As an Associate Clinical Research Manager in Denmark, you will be primarily accountable for the end-to-end performance and project management for assigned protocols in our Nordic countries – namely, you will be leading cross-border country study teams across the Nordics.

As for main responsibilities you will be:

  • The main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).
  • Responsible for project management of the assigned studies: pro-active planning, driving and tracking execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close out.
  • Review Monitoring Visits Reports and escalate performance issues and training needs to CRA manager and/or functional vendor and internal management as needed.
  • Perform quality control visits as required
  • Lead local study teams and cross-border study teams to high performance: trains in the protocol other local roles, closely collaborates with and supports CRAs as protocol expert and coordinates activities across the different local country roles ensuring a strong collaboration
  • Responsible for creating and executing a local risk management plan for assigned studies
  • Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies

Requirements:

  • Bachelor’s degree in science (or comparable)

  • 4+ years of experience in clinical research

  • CRA experience preferred

  • Knowledge of Project Management

  • Ability to identify problems, conflicts, and opportunities early and lead, analyze and prepare mitigation plans and drive conflict resolution

  • Ability to negotiate skillfully in tough situations

  • Educational/pedagogic, diplomatic and empathic skills to effectively build and maintain professional relationships with investigators and other external stakeholders

  • Strong organizational skills with demonstrated success required

  • ability to make decisions independently and oversee important activities relevant to clinical research

  • strong understanding of local regulatory environment

  • Strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously.

  • Ability to communicates effectively and build a collaboration spirit in a remote/virtual environment and across countries, cultures and functions

  • Ability and skills to manage resource allocation, processes (and controls), productivity, quality and project delivery

  • Proficiency in written and spoken English and Danish

You are welcome to apply online – application deadline – August 9th.

Current Contingent Workers apply


Not Applicable


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A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.