Associate Clinical Research Manager

1 week ago

København, Denmark MSD Full time

Job Description

Our Clinical Research team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

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.

If you are already a CRM or in a CRA/Senior CRA role or similar and would like to develop further professionally and career-wise in a global research-focused environment, this may be a perfect opportunity for you

Main Responsibilities:

  • 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, and 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 communicate 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.

Your role at our company is integral to helping the world meet new breakthroughs that affect generations to come, and we're counting on your skills and inventiveness to help make meaningful contributions to global medical advancement.

Application:

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

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

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