Current jobs related to Preclinical-Clinical Project Manager - Copenhagen, Copenhagen - Black Swans Exist


  • Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time

    Department OverviewThe Department of Preclinical Fluid Biomarkers and Occupancy is a key part of Lundbeck's Research and Development organisation. We are responsible for generating strong in vivo pharmacology data packages for new drug candidates in Lundbeck's R&D pipeline.About the RoleThis position involves contributing to the development of early drug...


  • Copenhagen, Copenhagen, Denmark beBee Careers Full time

    In this challenging and dynamic role, you will lead the execution of clinical projects in assigned therapeutic areas across all countries in Region Europe & Canada (EUCAN). Key responsibilities include leading strategic planning with countries, coordinating trial portfolio review, and ensuring alignment with global trial planning.The ideal candidate will...


  • Copenhagen, Copenhagen, Denmark beBee Careers Full time

    Job Overview:">We invite experienced professionals to join our team as Senior Life Science Business Consultants. You will lead clinical IT projects, analyze client needs, translate them into specific solutions, and ensure successful project outcomes. This role requires a strong understanding of the life science sector, excellent communication skills, and...


  • Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time

    Scientist (maternity cover), Department of Preclinical Fluid Biomarkers and OccupancyRequisition ID: 6222Location: Copenhagen, Danish Capital Region, DKScientist (maternity cover), Department of Preclinical Fluid Biomarkers and OccupancyAre you a highly motivated Scientist with a strong interest in Translational Biology, experience with immunoassays and...


  • Copenhagen, Copenhagen, Denmark beBee Careers Full time

    Clinical Program Lead Role OverviewAs a key member of our Global Clinical Development team, the Clinical Program Lead will play a pivotal role in bridging the clinical aspects of our organization.The successful candidate will have excellent stakeholder management skills and be able to navigate complex landscapes to drive clinical development programs...


  • Copenhagen, Copenhagen, Denmark Genmab AS Full time

    About the RoleGenmab A/S is seeking a highly skilled (Senior) CMC Technical Integration Manager to join its dynamic team in New Product Introduction (NPI) CMC. The successful candidate will be responsible for developing and supporting analytical/process strategies for selected projects within the Genmab Early-Stage project portfolio.The NPI CMC Team covers...


  • Copenhagen, Copenhagen, Denmark beBee Careers Full time

    Leading Global Clinical TrialsWe are seeking an experienced Clinical Trial Manager to join our global clinical operations team. As a key member of the team, you will be responsible for leading trial management teams, managing CROs and vendors, and ensuring timely and cost-effective delivery of clinical trials.The successful candidate will have a strong track...


  • Copenhagen, Copenhagen, Denmark Novo Nordisk AS Full time

    Required Skills and QualificationsBachelor's Degree, Master's degree, or PhD in Life Sciences.Advanced Clinical Research Associate and project management level, trained in Good Clinical Practice.Minimum 5 years of working experience in clinical project management.Solid knowledge of clinical development processes.Fluent in written and spoken English.The ideal...


  • Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time

    Lundbeck A/S, H is seeking a highly motivated Scientist (maternity cover) to join our Department of Preclinical Fluid Biomarkers and Occupancy.The ideal candidate will have a strong background in translational biology, experience with immunoassays and bioanalysis, and a solid understanding of biomarker applications.In this temporary position, you will...


  • Copenhagen, Copenhagen, Denmark TruLab, Real-Time Technology for Clinical Trial Oversight Full time

    TruTechnologies is an RTP-based mobile technology company that provides biosample tracking and management solutions for clinical trials. TruTechnologies' mission is to eliminate loss of samples provided for research by patients. The TruTechnologies solution empowers drug developers to track biosamples from the point of collection in real-time and ensure...

Preclinical-Clinical Project Manager

2 weeks ago


Copenhagen, Copenhagen, Denmark Black Swans Exist Full time

Get AI-powered advice on this job and more exclusive features.

Delivery Manager | Process Development | Life Science Recruitment

Preclinical-Clinical Project Manager

Introduction & Purpose

  • Serve as Program Leader for one or more cross-functional program teams, providing strategic leadership and serving as the primary point of accountability for the program.

Essential Responsibilities & Scope of the Job

Including, but not limited to:

  • Manage program-wide timelines and budgets .
  • Ensure clarity of mission and accountability for critical program objectives and alignment with corporate goals.
  • Proactively define (with cross-functional development team) program strategy, goals, decision points , and potential risk areas, including mitigation strategies.
  • Clearly define team structure, roles, and responsibilities to meet program goals and facilitate coordination across functions.
  • Identify the need for external expertise and engage outside experts as necessary.
  • Serve as primary spokesperson for the program, regularly communicating progress and issues to key stakeholders, senior management, and external advisory committees.
  • Foster a team culture of ownership, continuous evaluation, and improvement , ensuring recognition of team achievements.
  • Contribute expertise to the development and evolution of the program management function to further business needs.
  • Facilitate collaboration with potential partners in close collaboration with management

Position Qualifications (Knowledge, Skills, Abilities, Education, Experience)

  • Independent, capable of multi-tasking effectively , and results-oriented with a hands-on approach suited for a fast-paced and dynamic environment.
  • Ability to contribute meaningfully and strategically as a partner to cross-functional teams.
  • Maintains the highest standards of integrity and ethical behavior in all business affairs.
  • Smart, innovative, and forward-thinking while remaining pragmatic and operational, with a strong commitment to patients and science .
  • Exceptional communication skills , both oral and written.
  • Ability to influence outcomes internally and externally while maintaining positive relationships.

Requirements:

  • A highly motivated, goal- and results-oriented individual with a Master's degree or equivalent .
  • At least 5 years of experience as a Program Leader and/or Manager in drug development programs (global drug development experience is a plus).
  • Thorough understanding of the drug development process and knowledge of key functional activities.
  • In-depth knowledge of Program and Project Management principles and practices .
  • Demonstrated ability to lead in a cross-functional, interdisciplinary environment .
  • Proven ability to drive high-level decision-making .
  • Excellent interpersonal, oral, and written communication skills .

Additional Comments:

  • Ability to strategically and operationally manage multiple vendors and external business partners .
  • Strong scientific acumen and oral communication skills.
  • Ability to interpret medical and scientific literature effectively .
  • Commitment to mission-driven work and core values .
Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Research

Industries

Pharmaceutical Manufacturing and Biotechnology Research

#J-18808-Ljbffr