About us

PASSION . EXPERIENCE . PARTNERSHIP

We have extensive experience in Oncology, Immunology, Rare diseases and Neurology.

AnRes Clinical is a highly specialised, expert, flexible, agile, and focused life science consultancy assisting biotech companies in gathering the relevant and high-quality clinical evidence that is necessary to gain Marketing Authorisations for their products.


We are a close-knit team of extremely passionate and devoted clinical research professionals with a wealth of experience.

In our collaborations, we become a natural extension to the team bringing relevant expertise coupled with a partnering mindset.


In our approach, we are focused on linking the science with pragmatic operational aspects

of clinical development. This combined with the understanding of the complex regulatory framework, makes us excellent partners when every step forward matters and needs to be carefully thought through.


VALUES CLOSE

TO OUR HEART 



  • Transparency and openness


  • Passion for clinical and scientific research


  • Determined – we strive to be the best at what we do


  • Integrity - we do the right thing


  • Partnership and close collaboration – we work as one team and respect each other

MISSION



To partner with biopharmaceutical companies, med-tech and Clinical Research Organisations in order to support development of better medicines.


VISION


 

To efficiently bring safer and more effective medicines to patients

CORE TEAM

Anna Polak-Andersen, M. Pharm

CEO / Clinical Development Expert

Experience:

  • Pharmacist by training with 16+ years of clinical project management and monitoring experience
  • Worked at both small and global CROs, most recently as Senior Associate Director at Medpace
  • Since founding AnRes Clinical in 2018, has led multiple development programs in Immunology, Rare Diseases, and Oncology.


Key Expertise:

  • Vendor set-up and oversight
  • Clinical study delivery from protocol design to TMF transfer
  • Program strategy and operational leadership
  • Global trial management across 30 countries and 5 continents

Annemarie Kleefstra, M.Sc.

Clinical Development Strategist

Experience:

  • 22+ years’ experience in drug development
  • Led various Rare disease, Oncology and Neuroscience trials


Core Expertise:

  • Program and project strategy & development
  • Trial Oversight
  • Protocol design& development
  • CRO and vendor selection

    Nanna Nielsen, cand.scient.Med

    Clinical Research Associate

    Denisa Hakunová, BA

    Marketing and Administrative Associate

    Natalia Małek

    Financial Analyst

    Experience:

    • Experience in monitoring activities for a prostate cancer trial, ensuring data integrity, site coordination, and compliance with GCP regulations
    • Background in cancer and immunological studies through academic research during her Master’s

     

    Core Expertise:

    • Clinical monitoring and site management
    • Data integrity and regulatory compliance
    • Building strong site–sponsor relationships
    • Ensuring transparent communication and collaboration

     

    Experience:

    • Skilled in business development, marketing, and organizational management focused on increasing productivity and team efficiency
    • Experience working across multicultural environments and diverse industries
    • Strong foundation in education and communication, drawing from her background as a teacher of English, Art, and Mathematics

     

    Core Expertise:

    • Business development and client communication
    • Marketing strategy and brand management
    • Cross-functional coordination and project organization
    • Building efficient systems to support team productivity

     

    Experience:

    • 5+ years’ experience in finance, administration, and process automation
    • Worked in global CRO and corporate training industries supporting operational efficiency and client relations
    • Technology & Automation Analyst at AstraZeneca — developing automations in Power BI, Power Automate, and VBA


    Core tasks:

    • Financial and administrative coordination
    • Process automation and digital training support
    • Budget preparation and invoicing
    • Operational support for clinical trial delivery

    Mette Hansenholt, M. Scient. Med.

    Clinical Research Associate

    Experience:

    • 2+ years’ experience in clinical start-up delivery at a global CRO
    • Worked across all Nordic countries, primarily in Rare Disease studies
    • Served as a key liaison between sites and sponsors, ensuring smooth study communication and delivery


    Core Expertise:

    • Document quality control and study process oversight
    • Start-up coordination and timeline management
    • Bridging operational and scientific aspects of drug development
    • Supporting lean biotech teams with adaptable project execution

    LET´S INNOVATE TOGETHER

    COLLABORATE

    We are always looking to talk to passionate experts sharing our values. If you enjoy working in a complex, dynamic and not always structured environment, aim at making decisions based on facts and scientific data and want to make an impact with your contribution being visible and highly appreciated,

    DO GET IN TOUCH!

    We continue to expand our network of potential partners and collaborators. If you are offering a unique service or simply want to network,

    WE WOULD LOVE TO CHAT WITH YOU.

    AnRes Clinical is open to flexible employment including part-time work, so you can give your best at your job while enjoying the time with your loved ones and feeling in control of your workload.