Clinical Research Coordinator

Clinical Research Coordinator (Full‑time)

We are seeking a full‑time Clinical Research Coordinator with a minimum of 1 year of clinical experience. Someone with a strong interest in the clinical research field would be an excellent fit for our entry–level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail oriented, able to maintain organized records, and motivated to learn new things as our company is always growing and expanding into new therapeutic areas.

• Participates in research participant screening, recruitment and enrollment; consents and conducts research visits for data collection + minimal–risk trials with oversight; responsible for collecting, processing and shipping of research specimens, where applicable.
• Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits; obtains, reviews and maintains source documents.
• Maintains organization of all trial related documents and correspondence; implements quality control and assurance methods.
• Communicates with study sponsors, research team and the Institutional Review Board; assists with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
• Maintains professional and technical knowledge about clinical trials.
• Communicates with research participants/families, protecting patient confidentiality.

• Bachelor’s degree in a health‑related field with one to two years relevant clinical experience OR Master’s degree in a medical related field with no research experience.
• Phlebotomy skills preferred.
• Psychology experience with knowledge regarding psychiatric rating scales preferred.
• National Certification (CRA or ACRP), BLS Certification.
• Expert database and computer skills:
  Microsoft Office (Word, Excel, Outlook); excellent verbal and written communication skills; ability to work independently and assume responsibility; excellent organizational skills; ability to meet data deadlines and maintain confidentiality; maintain data integrity within the department; work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff; knowledge of FDA Regulations and Good Clinical Practices.