A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 70,000 employees advance life-changing medicines across a wide range of therapeutic areas.

In this role, you will work with our renowned key sponsors and advance the development of innovative, life-changing medications for a variety of therapies.

If you are looking to broaden your therapeutic expertise whilst gaining exposure, taking on responsibility and developing your career within a world-class pharmaceutical working environment, this is an excellent opportunity!

What we have to offer:

• work as part of a diverse and stable team
  
• in-depth onboarding, including personal support from your mentor
  
• flexible working hours and compensatory time off in lieu
  
• a permanent employment contract
  
• travel time = work time
  
• highly competitive compensation packages including local allowances and additional insurances
  
• regular, merit-based salary adjustments
  
• significant employer contributions to an attractive pension scheme
  
• excellent training and career development opportunities
  
• strong support from Line Management, your team and more than 20'000 colleagues worldwide
  
• the world's most renowned pharmaceutical companies and innovative biotech pioneers as our satisfied, repeat customers for many years
  

Your responsibilities:

• Own all aspects of site management as described in the project plans
  
• Ensure the study staff conducting the protocol receive all materials and instructions to safely enter patients into the study
  
• Protect study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible entries
  
• Perform the required monitoring tasks in an efficient manner, according to SOPs and established guidelines; prepare accurate and timely trip reports
  
• Review progress of projects and initiate appropriate actions to achieve target objectives
  
• Interact with internal work groups to evaluate needs, resources and timelines
  
• Act as contact for clinical trial suppliers and other vendors as assigned
  
• Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  
• Independently perform CRF reviews
  
• Generate queries and resolve issues according to data review guidelines on Labcorp or sponsor data management systems
  

Your profile:

• Degree in a relevant field such as life sciences, pharmacology, biology, chemistry, health care, health management, (veterinary) medicine, nursing, etc.; in lieu of the former, a completed vocational education or professional experience (e.g. as study nurse, study coordinator...)
  
• Professional experience in a related function with a focus on independent site monitoring in Denmark
  
• Familiarity with applicable Danish and international regulatory requirements such as ICH / GCP
  
• Computer literacy in Microsoft Office (Word, Excel, PowerPoint) and preferably in relevant software solutions for clinical trials, e.g. eTMF (e.g. Veeva Vault)
  
• Effective time management and organizational skills and a keen attention to detail
  
• Valid driver's license
  
• Excellent communication skills in business fluent Danish and English - both spoken and written - are a must
  

REMOTE

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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