Cardiovascular Clinical Research Coordinator
35–45 an hour
Behavioral Health Market Context
Apply Nowvia Indeed
Benefits
Health InsurancePaid Time OffDental Coverage
Job Description
Key ResponsibilitiesStudy Coordination & Oversight
• Develop a comprehensive understanding of assigned study protocols prior to study initiation
• Collaborate with Principal Investigator (PI) and Site Director to ensure protocol compliance
• Assist in the development and review of source documents and study materials
• Manage clinical studies with oversight from PI and Site Director
• Support patient recruitment strategies and enrollment initiatives
Patient Interaction & Study Execution
• Screen, enroll, and schedule study participants
• Obtain and document informed consent
• Coordinate and conduct study visits per protocol
• Monitor patient safety and report adverse events accurately
Data & Regulatory Management
• Maintain accurate, complete, and organized study records
• Enter data into electronic or paper data capture systems
• Document communications with sponsors, labs, and regulatory bodies
• Ensure compliance with IRB requirements, GCP, and regulatory standards
• Assist with study close-out procedures and record retention
Collaboration & Compliance
• Attend investigator meetings as required
• Work closely with physicians, site leadership, and sponsors
• Identify and report protocol deviations or issues
QualificationsEducation & Experience
• Active Registered Nurse (RN) license required
• 1–2 years of clinical research experience preferred
• Strong knowledge of medical terminology
Skills & Competencies
• Excellent communication and interpersonal skills
• Strong organizational and documentation abilities
• Ability to work independently and make sound decisions
• Proficiency in Microsoft Office (Word, Excel) and research software systems
Requirements
• Understanding of Good Clinical Practice (GCP) and ICH guidelines
• Ability to manage multiple priorities in a fast-paced environment
• High attention to detail and commitment to data integrity and patient safety
Why Join Us
• Work with a leading cardiovascular research team
• Opportunity to participate in cutting-edge clinical trials
• Collaborative and physician-led environment
Pay: $35.00 - $45.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Retirement plan
• Vision insurance
Work Location: In person
• Develop a comprehensive understanding of assigned study protocols prior to study initiation
• Collaborate with Principal Investigator (PI) and Site Director to ensure protocol compliance
• Assist in the development and review of source documents and study materials
• Manage clinical studies with oversight from PI and Site Director
• Support patient recruitment strategies and enrollment initiatives
Patient Interaction & Study Execution
• Screen, enroll, and schedule study participants
• Obtain and document informed consent
• Coordinate and conduct study visits per protocol
• Monitor patient safety and report adverse events accurately
Data & Regulatory Management
• Maintain accurate, complete, and organized study records
• Enter data into electronic or paper data capture systems
• Document communications with sponsors, labs, and regulatory bodies
• Ensure compliance with IRB requirements, GCP, and regulatory standards
• Assist with study close-out procedures and record retention
Collaboration & Compliance
• Attend investigator meetings as required
• Work closely with physicians, site leadership, and sponsors
• Identify and report protocol deviations or issues
QualificationsEducation & Experience
• Active Registered Nurse (RN) license required
• 1–2 years of clinical research experience preferred
• Strong knowledge of medical terminology
Skills & Competencies
• Excellent communication and interpersonal skills
• Strong organizational and documentation abilities
• Ability to work independently and make sound decisions
• Proficiency in Microsoft Office (Word, Excel) and research software systems
Requirements
• Understanding of Good Clinical Practice (GCP) and ICH guidelines
• Ability to manage multiple priorities in a fast-paced environment
• High attention to detail and commitment to data integrity and patient safety
Why Join Us
• Work with a leading cardiovascular research team
• Opportunity to participate in cutting-edge clinical trials
• Collaborative and physician-led environment
Pay: $35.00 - $45.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Retirement plan
• Vision insurance
Work Location: In person
Qualifications
- •QualificationsEducation & Experience
- •Active Registered Nurse (RN) license required
- •Strong knowledge of medical terminology
- •Excellent communication and interpersonal skills
- •Strong organizational and documentation abilities
- •Ability to work independently and make sound decisions
- •Proficiency in Microsoft Office (Word, Excel) and research software systems
- •Understanding of Good Clinical Practice (GCP) and ICH guidelines
- •Ability to manage multiple priorities in a fast-paced environment
- •High attention to detail and commitment to data integrity and patient safety
- •Opportunity to participate in cutting-edge clinical trials
Benefits
- •Work with a leading cardiovascular research team
- •Collaborative and physician-led environment
- •Pay: $35.00 - $45.00 per hour
- •401(k)
- •401(k) matching
- •Dental insurance
- •Health insurance
- •Life insurance
- •Paid time off
- •Parental leave
- •Retirement plan
- •Vision insurance
Responsibilities
- •Cardiology Partners Clinical Research Institute is seeking a motivated and detail-oriented Registered Nurse (RN) to serve as a Cardiovascular Clinical Research Coordinator
- •This role is responsible for managing clinical trials, ensuring protocol compliance, coordinating patient care, and maintaining high-quality research data in collaboration with physicians and research leadership
- •Key ResponsibilitiesStudy Coordination & Oversight
- •Develop a comprehensive understanding of assigned study protocols prior to study initiation
- •Collaborate with Principal Investigator (PI) and Site Director to ensure protocol compliance
- •Assist in the development and review of source documents and study materials
- •Manage clinical studies with oversight from PI and Site Director
- •Support patient recruitment strategies and enrollment initiatives
- •Patient Interaction & Study Execution
- •Screen, enroll, and schedule study participants
- •Obtain and document informed consent
- •Coordinate and conduct study visits per protocol
- •Monitor patient safety and report adverse events accurately
- •Data & Regulatory Management
- •Maintain accurate, complete, and organized study records
- •Enter data into electronic or paper data capture systems
- •Document communications with sponsors, labs, and regulatory bodies
- •Ensure compliance with IRB requirements, GCP, and regulatory standards
- •Assist with study close-out procedures and record retention
- •Collaboration & Compliance
- •Attend investigator meetings as required
- •Work closely with physicians, site leadership, and sponsors
- •Identify and report protocol deviations or issues
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