Clinical research coordinator’s job is to take clinical trials using good clinical practice. They should be done ethically and safety of patients should also be taken into consideration. Hence he or she must possess sound knowledge, education and practice for the same. All trials need to be scientifically sound and approved.
The clinical research coordinator must also be willing to visit patients and see to it that due care is taken.
SAMPLE FORMAT OF CLINICAL
RESEARCH CO-ORDINATOR
Michael Clayton
37th street,
Ipswich
U.K.
Cliniconacs@gmail.com
CONTACT NO: +35 458786545
MOBILE NO:+68 9845685456
CAREER OBJECTIVE:
To enhance my skills in serving Clinics and take care of medical health of people in this way.
PROFESSIONAL EXPERIENCE:
Worked with Aballon company as clinical research coordinator in year (2008- 2009).
OBJECTIVES OF CLINICAL RESEARCH CO-ORDINATOR:
-To see into rights, safety and well being of patients at large.
-Benefits outweigh risks for each patient.
-To see into latest designing in Clinics and that quality is maintained.
-All documents should be stored and kept so that they can be verified in future.
QUALIFICATIONS:
Have done diploma in clinical research and practice from The Royal Hospital School, Suffolk (2006-2008).
ACHIEVEMENTS:
A friendly society at North Dakota gave me a thanks giving award for best medical service to their society.
HOBBIES :
-Bike riding
-Playing water sports.
REFERENCE:
“Upon request”.
