Clinical Research Coordinator Job Description
Clinical Research Coordinator Job Profile and Description
A clinical research coordinator is responsible for overseeing and supervising the staff who carry out clinical trials in the health care industry.
Duties and Responsibilities
- A clinical research coordinator has to coordinate the functions of the different departments and workers who work for a clinical trial in investigating new health care medicines, technologies and procedures.
- He has to supervise the staff involved in the trial and ensure that protocol is being maintained.
- He has to ensure that the clinical trials that are being performed meet the criteria that have been set by the concerned Drug Administrative body.
- He has to see whether the data for trial is being maintained accurately.
- He has to assist in analyzing and interpreting the data for the trial.
- He has to report to the principal scientist, investigator or physician responsible for performing the trial.
- He has to fill out all the safety and regulatory paperwork required for the trial and make sure that they get submitted to the appropriate agencies and boards.
- He has to obtain tissue and bloods samples as and when necessary and collect information through interviews, questionnaires, test results and charts.
Skills and Specifications
- A clinical research coordinator should have a high level of coordination and organizational skills.
- He should possess good leadership skills as well.
- He needs to possess good analytical skills.
- Good problem – solving and researching skills are required.
- Excellent communication and interpersonal skills is a must to be successful in this profession.
Education and Qualifications
A Bachelor’s or a Master’s degree in fields such as nursing, chemistry, biology, public health or psychology is required for persons who want to become a clinical research coordinator. Any additional degree or diploma in the related field will prove to be helpful.