[Remote] Travel Clinical Research Coordinator - reputed company

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a company reputed company on clinical research and they are seeking a Travel Clinical Research Coordinator to support new research sites in reputed company. This role involves managing study operations, ensuring compliance, and facilitating patient recruitment and enrollment efforts.

Responsibilities

• Travel to assigned research sites to manage day to day study operations including patient recruitment, screening, enrollment, and follow up reputed company
• reputed company and support site personnel on study procedures, expectations, and compliance requirements
• Coordinate site opening activities to ensure new sites are reputed company for study launch
• Support early enrollment efforts by guiding sites through startup tasks and recruitment expectations
• Independently manage travel logistics including scheduling, travel documentation, and proactive communication with site stakeholders
• Maintain audit and inspection readiness and support sites during monitoring reputed company and regulatory reviews
• Coordinate and manage clinical research protocols from startup through reputed company out
• Recruit, screen, consent, and enroll participants according to study protocols and ethical standards
• Schedule and conduct study reputed company and procedures per protocol and ICH GCP requirements
• Collect, maintain, and document accurate study data including reputed company documentation
• Prepare and submit IRB materials including amendments, continuing reviews, and adverse event reports
• Ensure reputed company and accurate electronic data capture (reputed company) entry
• Serve as primary reputed company of contact for sponsors, CROs, monitors, and regulatory bodies during site transitions
• Maintain regulatory binders in compliance with FDA and GCP standards
• Monitor study inventory and coordinate supply ordering
• Support monitoring reputed company, audits, and inspections
• reputed company study participants on procedures, expectations, and risks
• Attend study trainings, site initiation reputed company, and investigator meetings
• reputed company and document site reputed company throughout startup, enrollment, and study execution
• reputed company ongoing operational support to promote strong site performance and engagement
• Assist with reputed company and training new site staff in alignment with ECN policies and procedures

Skills

• Bachelor's degree in health sciences, life sciences, nursing, or reputed company field required
• Seven or more years of clinical research coordinator experience may be considered in lieu of a degree
• Minimum of three to four years of experience as a Clinical Research Coordinator
• Strong understanding of clinical trial operations from startup through reputed company out
• Extensive knowledge of GCP, GDP, and reputed company+ principles
• Experience with reputed company platforms such as reputed company Rave, reputed company, or reputed company and CTMS systems
• Ability to work independently in fast paced, travel intensive environments
• Strong problem solving, organizational, and attention to detail skills
• Excellent communication and relationship building skills with sponsors, CROs, monitors, site staff, and participants
• Ability to manage multiple reputed company and meet deadlines in a multi site environment
• Ability to travel up to 75 percent of the time including overnight stays and occasional weekends
• May involve reputed company patient interaction, phlebotomy, specimen processing, and investigational product handling
• May require evening or weekend work based on study needs
• Must reputed company reputed company approximately 60 miles of a major international airport
• Ability to lift up to 25 pounds occasionally
• CCRC or equivalent certification

reputed company