PRINCIPAL DUTIES AND RESPONSIBILITIES:

I STUDY RELATED ACTIVITIES:

A. To provide nursing care to all subjects admitted to the clinic.

B. Collection and processing of blood samples

C. Recording of vital signs and electrocardiogram

D. Responsible for performing other trial related activities such as custodian, meal distribution and supervision, baggage check and body search, compliance check, ICF presentation, administration of investigational products, dosing supervision, alcohol breath test, urine scan for drugs of abuse and other assigned activities.

E. Storage and shipment of study samples.

F. Assist with any other unspecified study activities.

II GENERAL CLINICAL DUTIES:

A. Arrangement of phlebotomy station before blood collection.

B. Preparation of sample collection labels under direction of project coordinator and Investigator.

C. Labeling of vacationers and ria vials.

D. Screening of subjects for clinical studies.

E. Maintenance of the emergency equipments and medicines and stock update and maintenance of logs of clinic

F. Handling and management of biological waste.

III ADMINISTRATIVE DUTIES:

A. Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements.

Contact - Akash Zode - HR - Mobile number given below

This is a walk-in to proceed further contact HR at the venue on date and time mentioned.

Please contact the HR on the mobile number mentioned below.

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity.