Clinical Research Associate

Freelance Clinical Research Associate

Job Type: contract
Job Category: Clinical CRAs
Region: Europe
Area: Denmark Sweden
Location: Homebased
Salary: Competitive Hourly Rate
Posted: 30th September 2021
Ref: CT17

Barrington James is partnered with a small and well-established CRO based in Finland with operation sites in Sweden and Denmark, who are looking for a Freelance Clinical Research Associate to join their team and work on ongoing projects.
Working alongside some of the most talented individuals in the industry, this opportunity would be perfect for someone who is an experienced CRA with relevant experience working in the pharmaceutical industry. This role is mainly remote-based with site visits once every third month, providing you with flexibility while being based in Sweden, Denmark, or Norway.
Partnering with this company would give you the chance to work with a team that prioritises quality over quantity.



Site Selection

  • Participate in the evaluation and recruitment of suitable investigators
  • Prepare, conduct and report Site Selection Visits

Regulatory and Ethics Committee Submissions

  • Responsible for applications
  • Prepare and submit applications to the local Competent Authorities and Ethics Committee(s)

Informed Consent Form (ICF)

  • Ensure that country-specific ICF fulfills protocol and local requirements.


  • Responsible for setting up study files
  • Prepare, conduct and report Site Initiation Visits



  • Ensure that stipulated timelines and goals are met
  • Prepare, conduct and report Site Monitoring Visits


Study Close-Out

  • Prepare, conduct and report Site Close-Out Visits

In addition responsibilities of the CRA include, but are not limited to, the following tasks:

− Investigational Product management − Trial related logistics − Safety reporting within timelines − Reporting possible ICH GCP and protocol deviations − Identification of possible non-compliance with a resolution − Managing trial filing and archiving − Training, supporting and mentoring trial site team in trial-specific procedures − Managing site related activities associated with audits and regulatory inspections − Taking initiative and suggesting changes to improve procedures, working routines and cost savings

If you are interested in this opportunity, message me via my LinkedIn profile

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