Work SiteThis is a fully on-site position in Orlando, Florida Qualifications MUST have Neurology experience within the Clinical Research space Bachelor’s degree in Healthcare Administration, Research, or related field with a minimum of 3 years’ of Clinical Research experience Neurology Clinical Research Coordinator II
Conducting patient recruitment, patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs.
Coordination of bio-specimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance.
Execute and coordinate the informed consent process for client’s 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.
Provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies.
Coordinate or perform bio-specimen collection (i.e. blood, tissue) and maintain HIPAA protected database connecting patient information to bio-specimens used in research; perform patient chart review and data collection.
Collaborative interaction with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices, to ensure ongoing regulatory and protocol compliance.
Through collaboration with assistant clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems.
Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents.
Serves 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 Institutes research division intended to meet standards.
Ensures all patient-facing activities are compliant with clinical research standards and client 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.
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
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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] (%[email protected]) for other accommodation options.