Nesco Resource
Clinical Research Coordinator (Onsite)
Nesco Resource, Nashville, Tennessee, United States, 37247
Clinical Research Coordinator
Schedule: Monday–Friday, 7:00 AM – 4:00 PM or 8:00 AM – 5:00 PM
Health Requirements: None
Travel: Occasional (up to 25%)
Qualifications:
Bachelor's Degree (required)
1 year of relevant clinical research or healthcare experience (required)
Certified Clinical Research Coordinator (CCRC) preferred
Or equivalent combination of education and experience
Major Responsibilities:
Adhere to the Code of Conduct, Mission, and Values of the organization
Complete assigned training by due dates
Perform routine operational activities across multiple research protocols
Serve as liaison between site staff, sponsors, and leadership
Collaborate with departments including finance, hospital administration, and IRB (if applicable)
Coordinate study assessments from feasibility through closeout
Review study design and eligibility with physician and patient
Ensure proper informed consent and protocol compliance
Verify accuracy and completeness of data through source documentation review
Create study-specific documentation tools when not provided
Enter study data into case report forms and electronic systems
Manage and track study-related supplies, drug, and device shipments
Track and report adverse events, deviations, waivers, and violations
Communicate protocol-related updates to study staff and management
Participate in site meetings, investigator meetings, and CRC group calls
Review and respond to monitoring and audit findings
Knowledge, Skills & Abilities:
Knowledge: Organizational policies and standard operating procedures (SOPs)
ICH guidelines and Code of Federal Regulations
Basic medical terminology
Skills: Effective written and verbal communication
Strong time management and organizational abilities
Basic clinical trial techniques (ECG, phlebotomy, specimen handling)
Abilities: Strong interpersonal and problem-solving skills
High attention to detail
Self-motivated and accountable
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr
Bachelor's Degree (required)
1 year of relevant clinical research or healthcare experience (required)
Certified Clinical Research Coordinator (CCRC) preferred
Or equivalent combination of education and experience
Major Responsibilities:
Adhere to the Code of Conduct, Mission, and Values of the organization
Complete assigned training by due dates
Perform routine operational activities across multiple research protocols
Serve as liaison between site staff, sponsors, and leadership
Collaborate with departments including finance, hospital administration, and IRB (if applicable)
Coordinate study assessments from feasibility through closeout
Review study design and eligibility with physician and patient
Ensure proper informed consent and protocol compliance
Verify accuracy and completeness of data through source documentation review
Create study-specific documentation tools when not provided
Enter study data into case report forms and electronic systems
Manage and track study-related supplies, drug, and device shipments
Track and report adverse events, deviations, waivers, and violations
Communicate protocol-related updates to study staff and management
Participate in site meetings, investigator meetings, and CRC group calls
Review and respond to monitoring and audit findings
Knowledge, Skills & Abilities:
Knowledge: Organizational policies and standard operating procedures (SOPs)
ICH guidelines and Code of Federal Regulations
Basic medical terminology
Skills: Effective written and verbal communication
Strong time management and organizational abilities
Basic clinical trial techniques (ECG, phlebotomy, specimen handling)
Abilities: Strong interpersonal and problem-solving skills
High attention to detail
Self-motivated and accountable
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr