Clinical Research Coordinator II - Neurology

Actalent

Oct 28

Applications are closed

Job
Full-time
Junior & Mid Level
Research & Development
Healthcare
Orlando

Requirements

MUST have Neurology experience within the Clinical Research space

Responsibilities

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.

FAQs

Is this position remote or on-site?

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

What specific experience is required for this role?

Candidates must have Neurology experience within the Clinical Research space.

What are the main responsibilities of a Clinical Research Coordinator II in this role?

Responsibilities include conducting patient recruitment, screening, coordinating care and follow-up, managing bio-specimen collection, executing the informed consent process, and ensuring compliance with protocols and regulations.

Will there be any travel involved in this position?

Yes, this role may require travel between research sites and laboratories.

What type of services should the Clinical Research Coordinator provide to participants?

The Clinical Research Coordinator is expected to provide concierge-level service for all patient-facing interactions during clinical trials and research studies.

How will this role interact with other teams and departments?

The Clinical Research Coordinator will collaborate with Clinical Research nursing staff, laboratory teams, hospital departments, and physician offices to ensure ongoing regulatory and protocol compliance.

What is involved in the bio-specimen collection process?

The Clinical Research Coordinator will coordinate or perform bio-specimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to collected bio-specimens.

Will this role involve assisting with the development of research protocols?

Yes, the Clinical Research Coordinator will assist Principal Investigators and research staff in the development of compliant research protocols and other control documents.

What measures are in place to ensure diversity and inclusion at Actalent?

Actalent promotes diversity and inclusion through hiring diverse talent, maintaining an inclusive environment, building a culture of care and engagement, and ensuring growth opportunities for their people.

How can a candidate request accommodations during the application process?

Candidates can request reasonable accommodations by emailing actalentaccommodation@actalentservices.com for assistance with the application or interviewing process.

Actalent

An Engineering and Sciences Services Company | People to Possible

Human Resources

Industry

5001-10,000

Employees

Mission & Purpose

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference. Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research. Actalent is an operating company of Allegis Group, the global leader in talent solutions.