Clinical Research Coordinator I- School of Medicine, Rheumatology

Emory • Atlanta, GA

1d • Hybrid

About The Position

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University on a flexible weekly schedule based upon business needs. Schedule is based on agreed upon guidelines of department. This role requires residency in the state of GA. Emory reserves the right to change remote work status with notice to employee.

Requirements

• High School Diploma or GED and three years of administrative support experience.
• Two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
• Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
• A Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
• Experience with research coordination (e.g., recruitment, consent, interviewing, and data entry).
• Strong organizational, attention-to-detail, and interpersonal skills.
• Willingness to complete a phlebotomy course provided.

Nice To Haves

• Bachelor's degree (psychology, social science, or public health preferred but not required)
• Venipuncture blood collection experience preferred but not required.

Responsibilities

• Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
• Assists with patient recruitment.
• Attends study meetings.
• Orders and maintains equipment and supplies.
• Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
• Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
• Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
• Assists with quality assurance and tracks regulatory submissions.
• Performs related approved responsibilities as required.

Benefits

• Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level