Job Description

Clinical Research Assistant We are seeking a Clinical Research Assistant to support ongoing clinical trials. This is an excellent opportunity for individuals looking to gain hands-on experience in clinical research and contribute to meaningful advancements in healthcare. Responsibilities: Assist in coordinating various aspects of clinical trials, including study initiation, patient recruitment, and study visits. Serve as a liaison between investigators, study sponsors, and participants. Maintain accurate and up-to-date study documentation, including case report forms and regulatory files. Support the informed consent process and conduct patient screenings. Manage lab sample processing, including packaging and shipping specimens. Schedule and oversee study-related patient visits to ensure protocol compliance. Adhere to Good Clinical Practice (GCP) guidelines and regulatory requirements. Qualifications: High school diploma required; a Bachelor’s degree is preferred. Two to five years of experience in a clinical setting is a plus. Phlebotomy experience or certification is preferred. Familiarity with medical terminology and electronic medical records is beneficial. Strong attention to detail, organizational skills, and ability to work independently and collaboratively. Benefits: Competitive compensation Comprehensive health, dental, vision, life, and disability insurance Paid time off Professional development opportunities This is a full-time, on-site position with occasional travel to partner sites. If you are interested in gaining experience in clinical research and making an impact in the field, please apply or reach out for more details.

Job Tags

Full time,

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