Clinical Research Coordinator

Clinical Research Coordinator (CRC)Location: Florida, Texas, California, North Carolina, Illinois, Tennessee (Multiple locations to choose from)Employment Type: Full-TimeIndustry: Clinical ResearchAbout the OpportunityA growing and well-established clinical research organization is seeking an experienced Clinical Research Coordinator (CRC) to join their team. This individual will play a key role in supporting Phase I–IV clinical trials by managing study operations, ensuring protocol compliance, and providing high-quality patient care throughout the research process.This is an excellent opportunity to join a collaborative team environment with strong leadership and continued growth.Key ResponsibilitiesCoordinate and manage clinical trials in accordance with protocol, GCP, and regulatory requirementsScreen and recruit study participants, including reviewing medical history and determining eligibilitySchedule and conduct subject visits, including collecting vitals and performing study-related proceduresMaintain accurate source documentation and ensure timely data entry into EDC and CTMS systemsCommunicate effectively with Principal Investigators, Sponsors, CROs, and study team membersAssist with query resolution and monitor/audit preparationProcess and ship laboratory specimens per protocol requirementsMaintain investigational product accountability and documentationEducate study participants and provide ongoing support throughout the trialIdentify and escalate protocol deviations or operational challengesRecruitment & Study SupportSupport recruitment initiatives and collaborate with internal recruitment teamsProvide regular enrollment updates and participate in study start-up activitiesAssist with study materials, patient outreach, and retention strategiesQualificationsMinimum 2+ years of Clinical Research Coordinator experienceExperience working on industry-sponsored clinical trials preferredKnowledge of FDA regulations, ICH-GCP, and clinical trial processesPhlebotomy, ECG, and patient-facing clinical skills preferredCCRC or CCRP certification is a plusSkills & CompetenciesStrong organizational and multitasking abilitiesExcellent communication and interpersonal skillsDetail-oriented with strong documentation practicesAbility to work independently and within a team environmentComfortable working in a fast-paced clinical research settingProficiency with EDC, CTMS, and Microsoft OfficeWhy Apply?Opportunity to join a reputable and growing research organizationCollaborative and supportive team environmentCompetitive compensation packageCareer growth and development opportunities