Medical Records Research Coordinator is responsible for organizing and overseeing the record keeping activities pertaining to releasing and retrieving medical records for research projects. Ensures all medical records are tracked and released according to HIPAA guidelines. Being a Medical Records Research Coordinator may require an associate degree or its equivalent. Typically reports to a supervisor or manager. The Medical Records Research Coordinator possesses a moderate understanding of general aspects of the job. Works under the close direction of senior personnel in the functional area. May require 0-1 year of general work experience. (Copyright 2024 Salary.com)
We are a Clinical Research Company that specializes in conducting clinical trials and are looking to hire energetic, quick learners with basic medical skills to be a part of our team.
We will provide training for most of the job responsibilities.
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Research Director.
The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC will also work on patient recruitment, general administrative tasks, and data entry.
The Clinical Research Coordinator undertakes the performance of clinical trials. The individual seeking this position will be responsible for all aspects of completion of the research study.
Ideal candidate will possess good verbal and written communication skills, work well independently an ability to adjust and interact with various types of people. Must be a team player, maintain confidentiality, and be comfortable working in the medical field.
Candidate will demonstrate customer service that is compassionate, courteous, friendly, non-judgmental, and demonstrate a respect for privacy.
Previous experience in clinical research is a plus.
CRC duties include, but not limited to:
-Screens for subject eligibility for research protocols; patient recruitment-Maintains records for clinical study and regulatory documents.
-Performs blood work, EKGs/ECGs and other clinical procedures on study participants.
-Coordinates and schedules research subject appointments for tests and procedures.
-Corresponds with research subjects throughout the study
-Obtains, reviews, and records medical history for the subject during the duration of the trial
-Communicates with subjects and/or caregiver regarding medication changes, adverse events, scheduling visits, and study drug compliance.
-Administers scales, diagnostic testing, and other study assessments.
-Composes and types study correspondence and other source documentation
-Collects and enters data into study database
-Perform other tasks as assigned.
Job Type: Full-time
Pay: $18.00 - $22.00 per hour
Expected hours: 40 per week
Benefits:
Medical specialties:
Schedule:
Work setting:
Education:
License/Certification:
Work Location: In person
Clear All
0 Medical Records Research Coordinator jobs found in Saginaw, MI area