Clinical Research Associate

3 weeks ago

Uppsala, Uppsala, Sweden Pharmiweb Full time
Job Description

As a Clinical Research Associate at ICON, you will be partnering with a global pharmaceutical company to manage clinical trials in Sweden. This role involves working independently to set up and monitor studies, complete reports, and maintain documentation.

Key Responsibilities:

  • Setting up and monitoring studies, including study start-up and close-out
  • Completing reports and maintaining documentation
  • Submitting protocol, consent documents for ethics/IRB approval, and preparing regulatory submissions
  • Balancing sponsor generated queries
  • Taking responsibility for study cost efficiency
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs

Requirements:

  • 3 years of monitoring experience in phase I-III trials as a CRA
  • College degree in medicine, science, or equivalent
  • Previous monitoring experience in medium-sized studies, including study start-up and close-out
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
  • Excellent written and verbal communication
  • Ability to work to tight deadlines
  • Availability to travel at least 60% of the time (international and domestic) and possession of a valid driving license
  • Local language experience

What ICON Offers:

  • Competitive salary
  • Range of health insurance offerings
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme
  • Life assurance
  • Flexible country-specific optional benefits

At ICON, diversity, inclusion, and belonging are fundamental to our culture and values. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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