Project Coordinator L Pt Flex
LOCATION
Part Time Flex - Monday-Friday
QUALIFICATIONS
Bachelor's Degree required, with 1-3 years of experience preferred; certifications such as CCRP, CCRA, or ACRP-CP are preferred.
RESPONSIBILITIES
Manage research projects, train and supervise staff, assist in project data management, coordinate meetings, promote projects, and prepare regulatory documentation while ensuring compliance with grant criteria.
INDUSTRY
Clinical Research
SHORT DESCRIPTION
The Clinical Research Project Coordinator I provides administrative support for research projects, manages recruitment, oversees daily operations, and ensures compliance with regulatory standards.
Clinical Research Project Coordinator I provides supervision and non-clinical administrative support for the project. Responsible for initiating and maintaining recruitment, managing daily operations, monitoring for continued support for the project. This position coordinates the daily activities, assists with processing applicants, and tracks the progress of study participants. Maintains data required by sponsors, and serves as a resource to all entities/individuals involved in the program. Assists with marketing initiatives and web-site maintenance, and ensures compliance with all grant criteria.
Job Description:
1. Responsible for the management of research project(s)
2. Trains and supervises project specific staff (Clinical Research Assistants I-III, volunteers, students, consultants, etc); records HR issues as needed
3. Assists in the planning, implementation, and management of project data
4. Promotes the project(s) through marketing, website, other sources, etc.
5. Coordinates project meetings including creating agendas and drafting minutes
6. Collaborates on presentations, publications, and dissemination of project results, as requested
7. Supervises biospecimen collection, packaging, shipping, and infection control procedures
8. Aids in preparation of IRB protocols, amendments, annual reviews, risk assessments, adverse event reports, and informed consent documents; communicates with IRB throughout submission and review process
9. Supports Investigator in preparing regulatory reports, including convening DSMB meetings and writing DSMB reports, and assisting with NIH RPPRs
Additional Responsibilities:
Excellent communication skills and analytic abilities • Basic computer skills, e.g. familiarity with Microsoft software, completing spreadsheet/data entry. • Ability to work with diverse populations and support an inclusive, culturally responsive environment.
Education:
Bachelor's Degree required
Minimum 1-3 years experience
Certifications:
CCRP, CCRA, or ACRP-CP preferred
Schedule:
20/40 Part Time Flex - Monday-Friday
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