Clinical Research Coordinator II (TRI)

Job Title: Clinical Research Coordinator II (TRI)

Job Description

The Clinical Research Coordinator (Non-RN) is involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities include:

• Execute and coordinate the informed consent process for research participants in clinical trials and research studies across multiple locations. This may require travel between sites and research laboratories, and/or the use of technology.
• Responsible for all aspects of research conducted including patient screening, assessing eligibility, and coordinating the participation and follow-up of volunteers placed on research studies, trials, and programs.
• Coordinate research participant recruitment and consenting for the therapeutic areas they serve.
• Provide concierge level service for all patient-facing interactions during the course of clinical trials and research studies.
• Coordinate or perform biospecimen collection (i.e. blood, tissue) and maintain a HIPAA-protected database connecting patient information to biospecimens used in research; perform patient chart review and data collection.
• Engage in collaborative interaction with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure ongoing regulatory and protocol compliance.
• Ensure compliant data entry/data mining into registries, patient records, and research-specific database systems through collaboration with assistant clinical coordinators.
• Assist Principal Investigators and research staff in the development of compliant research protocols and other control documents.
• Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.
• Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the Institute's research division to meet standards. Ensure all patient-facing activities are compliant with clinical research standards and procedures.
• Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.
  
  

Hard Skills

• Consenting
• Study management
  
  

Job Type

This is a permanent position.

Work Site

This is a fully on-site position in Orlando, Florida.

Benefits:

• Medical, Dental & Vision Plans
• 401k
• Paid Holiday & Vacations
• Employee Assistance Program
• Corporate discounts and much more!
  
  

Contact Us:

Please email a copy of your resume and 2-3 professional references to [email protected]

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people
  
  

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.