Pennsylvania

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Onsite

Job description

Job Summary

Premier Research is seeking a Clinical Research Associate I to become part of our Clinical Monitoring, Site Management, and SSU team in Pennsylvania. This role is pivotal in supporting our efforts in the biotechnology and medical technology sectors, contributing to the management of clinical trials and ensuring regulatory compliance.

Responsibilities

  • Assist in monitoring clinical trial sites to ensure adherence to study protocols and regulations.
  • Collaborate with site staff and sponsors to facilitate effective site management.
  • Contribute to the preparation and maintenance of study documentation.
  • Support the collection and reporting of trial data.

Qualifications

  • A licensed healthcare professional, such as a registered nurse, is preferred.
  • Equivalent work experience in a clinical or research setting may be acceptable.
  • Strong communication skills and the ability to work collaboratively within a team.
  • Detail-oriented mindset with a focus on data accuracy and compliance.

Premier Research 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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Clinical Research Associate I
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