Richmond, Virginia, 23219

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Onsite

Job Summary

The position of Clinical Research Associate II is open across all US locations, with the Richmond, Virginia office serving as a primary site. This role is conducted onsite, focusing on advancing global health through a variety of clinical trials and related consulting efforts. The CRA plays a pivotal role in managing sites and ensuring successful trial conduct.

Responsibilities

  • Oversee the management of clinical trial sites to ensure compliance with protocols.
  • Facilitate the close-out procedures of assigned investigator sites efficiently.
  • Monitor patient safety throughout all stages of the clinical trials.
  • Engage in continuous communication with trial stakeholders to uphold quality standards.

Qualifications

  • Proven experience in clinical research, ideally as a CRA in a similar capacity.
  • Strong understanding of clinical trial processes and regulatory requirements.
  • Excellent communication and organizational skills to manage multiple tasks effectively.

Parexel 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.
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Back to Top Clinical Research Associate II – All US Locations – FSP
Clinical Research Associate II – All US Locations – FSP
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supports..pdf, .doc, .docx, or .txt file