Clinical Research Coordinator

About Treasure Valley Medical Research

Treasure Valley Medical Research is committed to expanding therapeutic options and improving patient access to the latest treatments in the Boise area. The organization emphasizes personalized care, ensuring each study participant's unique medical situation is taken into account. By conducting cutting-edge clinical trials, they contribute to integrating innovative therapies into routine healthcare. The team works collaboratively with medical professionals and sponsors to enhance medical knowledge, prioritizing patient safety, quality, and outcomes.

Role Overview

The Clinical Research Coordinator is a full-time position based on-site in Boise, ID. This role involves managing day-to-day clinical trial operations such as coordinating participant screening and enrollment, obtaining and documenting informed consent, and ensuring adherence to protocols and regulatory standards. Key responsibilities include scheduling and conducting study visits, accurate data collection and entry, maintaining thorough study documentation, and monitoring participant safety. The coordinator will maintain regular communication with investigators, sponsors, clinical monitors, and clinic staff, assist with Institutional Review Board (IRB) submissions and other regulatory paperwork, ensuring studies are conducted efficiently and comply with Good Clinical Practice and organizational policies.

Qualifications and Skills

• Capable of managing and thoroughly documenting informed consent procedures, ensuring participants understand and voluntarily agree.
• Experienced in following and implementing study protocols to maintain compliance.
• Skilled in data collection, thorough documentation, and meticulous research activities related to clinical trials.
• Previous clinical research experience including coordinating patient visits, handling regulatory responsibilities, and maintaining study records.
• Knowledgeable about clinical trials' processes, timelines, regulatory frameworks, and collaboration with sponsors and monitors.
• Familiar with Good Clinical Practice (GCP), HIPAA, and other relevant regulatory guidelines.
• Effective communication abilities and teamwork skills to interact with multidisciplinary teams and participants.
• Strong organizational aptitude and time management to juggle multiple studies and tasks efficiently.
• Proficiency with electronic data capture platforms and basic computer tools such as electronic health records, spreadsheets, and databases.
• Holds an associate's or bachelor's degree in a health-related or life sciences field or possesses equivalent professional experience. Clinical research certification is advantageous.