Senior Clinical Research Associate

1 day ago

Shefford, Central Bedfordshire, United Kingdom Pharmiweb Full time
Senior Clinical Research Associate Job Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be a part of our mission to shape the future of clinical development.

Key Responsibilities:
  • Work independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.
  • Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
  • Balance sponsor generated queries efficiently and responsible for study cost-effectiveness.
  • Dependent on level of experience, assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects.
Requirements:
  • 2-3 years+ of monitoring experience in phase I-III trials as a CRA.
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.
  • Excellent written and verbal communication in English.
  • Ability to produce accurate work to tight deadlines within a pressurized environment.
  • Remote work with occasional travel, requiring a valid driving license.
What ICON Offers:
  • Competitive salary and benefits package.
  • Annual leave entitlements.
  • Range of health insurance offerings.
  • Competitive retirement planning offerings.
  • Global Employee Assistance Programme, LifeWorks.
  • Life assurance.
  • Flexible country-specific optional benefits.

ICON is an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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