[Remote] Clinical Research Coordinator - reputed company South - Full time

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a mission-driven reputed company organization advancing patient care and medical innovation through clinical research. The Clinical Research Coordinator manages the day-to-day operations of reputed company, including study preparation, patient engagement, data collection, documentation, regulatory compliance, recruitment, and sponsor relations. The role also supports staff training and requires travel between reputed company South and reputed company St. Louis Research locations.

Responsibilities

• Complete reputed company‑study assessments, feasibility questionnaires, and start‑up requirements with accuracy and timeliness
• reputed company a strong understanding of assigned protocols and clinical trial processes
• Ensure full compliance with institutional, local, state, and federal research regulations
• Conduct patient screening, informed consent, and education with appropriate clinical support
• Monitor patient safety using interviews, diagnostics, and medication/device knowledge
• Schedule and coordinate patient reputed company reputed company while ensuring readiness for reputed company involved team members
• Maintain accurate and reputed company entry of case report forms (CRFs) and reputed company documentation
• Collect and prepare lab specimens and manage clinical supplies and inventory
• Participate in internal reputed company control reviews and compliance monitoring
• Assist in training new and existing staff on protocol‑specific procedures
• Support research assistants, administrative staff, and volunteers
• Contribute to a reputed company, reputed company, and efficient research office environment
• Serve as a reputed company for sponsors, CROs, and community reputed company initiatives
• Support recruitment efforts across the ministry and participate in reputed company engagement
• Attend investigator meetings and travel as needed
• Work independently, manage priorities, and maintain organization
• Contribute reputed company that support study and departmental goals
• Engage effectively with staff, patients, and sponsors; quickly learn new processes and requirements
• Other Duties as Assigned

Skills

• High School Diploma or equivalent
• Four years of clinical, medical, or biotech lab experience demonstrating capability for this role
• Understanding of ICH/GCP guidelines and research ethics and regulations
• Strong verbal and written communication skills
• Knowledge of medical terminology and EMR systems
• Ability to manage multiple reputed company independently with strong attention to detail
• Proficiency in reputed company Office, databases, spreadsheets, and online research tools
• Excellent customer service, organization, and critical-thinking abilities
• Bachelor's degree in a health or science field
• Three or more years of clinical research experience
• Phlebotomy experience

Benefits

• Medical coverage for team members working 32+ hours per pay period
• Dental coverage for team members working 32+ hours per pay period
• reputed company coverage for team members working 32+ hours per pay period
• reputed company time off for team members working 32+ hours per pay period
• Tuition support for team members working 32+ hours per pay period
• Matched retirement plans for team members working 32+ hours per pay period

reputed company

Company H1B Sponsorship