Full Time Clinical Research Protocol Writer Jobs

Clinical Research Coordinator (Full-Time)Rocky Mountain Clinical Research ???? Idaho Falls, IDRocky Mountain Clinical Research is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team in Idaho Falls, ID. This is an excellent opportunity for a healthcare professional looking to expand into clinical research while making a meaningful impact on patient care and the future of medicine.If you enjoy working directly with patients, value precision and organization, and want to be part of a collaborative, mission-driven research organization, we encourage you to apply.???? Compensation & BenefitsHourly wage: $17 – $25 per hour (based on education, training, and experience)Benefits package includes:Medical, dental, and vision insurance401(k) retirement planPaid time off (PTO)Full-time, stable position with opportunities for professional growthAbout Rocky Mountain Clinical ResearchRocky Mountain Clinical Research was founded on the principle of advancing medical care for patients facing complex diseases. We conduct high-quality clinical research across a range of therapeutic areas, including diabetes, evaluating medications and medical devices to determine their safety and effectiveness compared to current standards of care.As an investigator-led, patient-focused research site, we play a key role in bringing new treatments to market while ensuring patient safety and regulatory compliance. We are a family-oriented organization that values teamwork, integrity, and long-term employee success.Position Summary: Clinical Research CoordinatorThe Clinical Research Coordinator plays a critical role in the day-to-day execution of clinical trials. Working closely with the Principal Investigator, Research Director, and study team, the CRC ensures that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), and federal regulations.This role combines patient interaction, clinical coordination, and administrative responsibilities, making it ideal for detail-oriented healthcare professionals who enjoy both people-facing and organizational work.Key ResponsibilitiesCoordinate and administer clinical trials under the direction of the Principal InvestigatorScreen, enroll, consent, and follow study participantsEnsure participant safety and protocol adherence throughout the study lifecycleMaintain accurate source documentation and regulatory filesComplete study-related data entry and follow-up documentation with high attention to detailPrepare for and support sponsor, monitor, and regulatory auditsCollaborate with investigators, sponsors, monitors, and internal research staffEnsure studies are conducted in compliance with GCP, FDA regulations, and study protocolsRequired QualificationsHealthcare or medical background (clinical or patient-facing experience)Strong clerical, organizational, and documentation skillsExcellent interpersonal and communication skillsHigh attention to detail and commitment to quality and accuracyAbility to work independently while collaborating effectively with a teamPreferred QualificationsCertified Medical Assistant (CMA), Licensed Practical Nurse (LPN), Registered Nurse (RN), or higher credentialingExperience in a healthcare, research, or clinical trial environmentFamiliarity with Good Clinical Practice (GCP), clinical trial protocols, or regulatory documentationStrong analytical and decision-making skillsClinical research experience is preferred but not required- GCP and CRC training will be provided for motivated candidates.Work ScheduleFull-timeMonday – FridayOccasional (but rare) weekends or major holidays requiredReady to Join Our Team?If you're passionate about patient care, clinical excellence, and contributing to the future of medicine, we'd love to hear from you. Join our team of 25 Clinical Research Coordinators where your work truly makes a difference.???? Apply today to become part of Rocky Mountain Clinical Research.We understand your time is valuable, so we have a very quick and easy application process. If you feel that you have the right medical or nursing background for this clinical study job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!Location: 83404