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Clinical Research Coordinator
POSITION SUMMARY
The Clinical Research Coordinator (CRC) is responsible for a variety of activities in support of clinical research studies. The CRC works closely with and carries out the directives of the Director of Clinical Research in all aspects of the care and treatment of clinical research subjects in compliance with study protocols throughout the research study. The CRC is responsible for his/her assigned portfolio of studies as it relates to but is not limited to, the following areas: protocol requirements; informed consent; recruitment; patient visits (paper and electronic); data entry; laboratory; test article; serious and non-serious adverse event reporting; and study close out. The CRC is required to have knowledge of protocol design and Good Clinical Practices (GCP) as set forth by the Federal Regulations and International Conference of Harmonization (ICH) Guidelines for the protection of human subjects and the conduct of clinical research required. Knowledge of the International Air Transport Association (IATA) regulations for the transportation of Dangerous Goods is also necessary. Under the direction of the Director of Clinical Research, the CRC will help ensure protocol compliance, Investigational Article accountability, and proper follow-up during the clinical trial.
TYPICAL PHYSICAL DEMANDS: Physically capable of lifting, moving, or transporting supplies, medical records, and equipment within reasonable weight limits. Physically capable of reading and reviewing handwritten chart notations. Physically capable of bending, sitting, or standing for extended periods of time, reaching, and climbing to retrieve or store medical records. Physically capable of manually entering data into an electronic database using a keyboard. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
TYPICAL WORK CONDITIONS: Fast-paced clinical research center environment. Must be able to adjust and adapt to changing conditions.
QUALIFICATIONS, REQUIREMENTS, and EDUCATION: Minimum: High School Diploma. Preferred: Associate degree in a medical-related field and one-year clinical research experience. The candidate will be required to sit for and successfully obtain CCRC or CCRP after two years of clinical research coordinator experience and maintain certification there and after. Travel within the USA to attend Investigator meetings for new clinical trials may be required.
ESSENTIAL SKILLS:
DUTIES AND RESPONSIBILITIES:
Clinical Trial Process:
Other:
Full Time
$48k-64k (estimate)
01/12/2024
05/03/2024
optimadermatology.com
<25
The job skills required for Clinical Research Coordinator include Clinical Research, Clinical Trial, Analysis, Planning, Scheduling, Collaboration, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator. You can explore the career advancement for a Clinical Research Coordinator below and select your interested title to get hiring information.