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Labcorp Drug Development

Start-Up Specialist - Denmark. Flexible location!


ID: 2183043
Indrykket for 160 dage siden

Job Details

This is an exciting position as the Start-Up Specialist in our transformational site readiness team, a blended start-up and regulatory role which offers the opportunity to develop across the full scope of the start-up process and allows you to have a real impact on people's health and lives.

If you are looking to take on responsibility and leverage your know-how in the start-up phase of clinical trials - ensuring a successful start of important clinical studies in Denmark -, this is the perfect opportunity.

What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.

Labcorp Drug Development has supported the pharmaceutical industry in developing more medicines worldwide than any other company, including the top best-selling drugs on the market today. Join us and see why more than % of the top global pharmaceutical companies are repeat customers!

This role is % home based, and the successful candidate can be based anywhere in Denmark. As such you must be a self-motivated and autonomous individual.

  • Degree in a relevant field such as pharmacology, life sciences, clinical trial management, (veterinarian) medicine, health care (management), nursing, chemistry, biology
  • In lieu of the above, an equivalent completed vocational education or equivalent professional experience

  • Experience:
  • Experience in clinical trials within a CRO or a pharmaceutical company with a specialization in clinical study start up / regulatory processes
  • Good understanding of research protocol requirements as well as the ability to communicate them / educate others about them
  • Ability to collaborate successfully with operational project teams as well as external investigative sites and local regulatory authorities (including IRBs and IECs)
  • Experience with submissions to the Danish regulatory authorities - observing all local regulations and guidelines as well as international standards such as ICH and GCP
  • Familiarity with investigator start-up documents and contract / budget negotiation processes with study sites
  • Autonomous work style with excellent time and project management skills
  • Business fluency in Danish & English - both spoken and written - is a must

  • Labcorp is proud to be an Equal Opportunity Employer:

    As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

    For more information about how we collect and store your personal data, please see our Privacy Statement .

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