Topeka, Kansas, 66612

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Onsite

Job Summary

Fortrea is on the lookout for a Clinical Research Associate II with a focus on Phase I clinical trials, to oversee various clinical trial sites situated in Texas and the Mid-West. This position will primarily involve ensuring that clinical trial protocols are adhered to and that data integrity is maintained throughout the research process.

Responsibilities

  • Conduct monitoring visits to clinical trial sites to verify protocol compliance.
  • Ensure data integrity through thorough oversight of collected data.
  • Manage site activities and maintain effective communication with site personnel.
  • Report serious adverse events in a timely and accurate manner.

Qualifications

  • Experience in clinical research, specifically in Phase I trials.
  • Strong understanding of clinical trial protocols and regulatory requirements.
  • Excellent communication skills to facilitate collaboration with site staff.
  • Ability to work effectively in a fast-paced environment and manage multiple tasks.

Fortrea provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
To apply for this job, please upload your resume.
supports..pdf, .doc, .docx, or .txt file
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Back to Top Clinical Research Associate II, Phase I – Texas/Mid-West
Clinical Research Associate II, Phase I – Texas/Mid-West
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supports..pdf, .doc, .docx, or .txt file