Clinical Research Coordinator

Tallahassee Memorial Healthcare•Tallahassee, FL

About The Position

Specialized research professional working with and under the direction of a Principal Investigator (PI) who is primarily responsible for overall design and conduct of research. Supports, facilitates, and coordinates daily clinical research activities and plays a critical role in conducting the study and associated regulatory compliance. Works with PI, department, sponsor, and institution to support and provide guidance on administering compliance, financial, personnel, and other related aspects of the clinical study. Reports directly to Director/Clinical Research/OI and indirectly (“dotted line”) to PI (who oversees incumbent’s day-to-day activities) and department service line administrator (SLA).

Requirements

Associate degree in allied health, health information management (HIM), nursing, public health, or equivalent
One (1) year of relevant job-related experience
Certified Clinical Research Coordinator (CCRC) credential from the Association of Clinical Research Professionals (ACRP) within three (3) years of employment required
Certified Clinical Research Professional (CCRP) credential from the Society of Clinical Research Associates (SOCRA) may be substituted for the CCRC credential

Nice To Haves

Bachelor’s degree in allied health, HIM, nursing, public health, or equivalent. Education in healthcare and/or research related fields.
Two (2) or more years of clinical research experience.
Working knowledge of medical terminology, anatomy, and physiology.
Understanding of regulations for Protection of Human Subjects, 45 Code of Federal Regulations (CFR) 46, and 21 CFR 50.
Understanding of Health Insurance Portability and Accountability Act (HIPAA) privacy rules and regulations.
Basic knowledge of data management.
Familiarity with data abstraction.
Excellent interpersonal skills with proven written, presentation, and verbal competencies.
High degree of planning and organizational skills.
Computer skills with demonstrated proficiency in Microsoft (MS) Word, MS Excel, MS PowerPoint, and MS Outlook.
Strong ability to work autonomously.
Strong ability to multi-task and manage competing priorities while demonstrating excellent customer service.
Ability to work well in a team, manage conflict, and resolve problems effectively.
Ability to attend routine study-specific research meetings and monthly research coordinator meetings.
CCRC credential at time of hire

Responsibilities

Supports, facilitates, and coordinates daily clinical research activities
Plays a critical role in conducting the study and associated regulatory compliance
Works with PI, department, sponsor, and institution to support and provide guidance on administering compliance, financial, personnel, and other related aspects of the clinical study

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