All India Institute of Medical Sciences, Raipur Invites Application for Clinical Research Coordinator Recruitment 2021

Vacancy Circular No:

All India Institute of Medical Sciences Raipur (AIIMS Raipur)
invites applications for recruitment of Clinical Research Coordinator

Clinical Research Coordinator

Number of Vacancy: 1 Posts

Educational Qualification: B.Pharma, B.Sc

Walk-in-interview will be conducted on 12.01.2022 for filling up of following posts in study titled "Study of correlation between serum copper, serum zinc, copper-zinc ratio, and disease severity scores in sickle cell disease patients" at AllMS Raipur, Chhattisgarh purely on contract basis:

1. Post Name: Clinical research coordinator

2. No. of Post: 01

3. Period of contract: The post will be initially for a period of six (6) Months extendable upto twelve (12) Months depending on candidates' performance.

4. Consolidated Salary (per month): 22,000/- (twenty-two thousand) Rupees per month

5. Essential Educational Qualification: Science graduate or Pharmacy graduate.(Clinical research diploma/degree holder will be preferred) The candidate should have minimum experience of six months as clinical research coordinator 

6. Essential Experience (if required): Good English communication skills. Good skills in reading handwritten Notes/ Doctor's prescription. Basic knowledge of medical terms and terminologies. Basic knowledge of Computer

7. Job Details: Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. Review informed consent document L procedures. Ensure accurate data entering and reporting maintain site source documents, medical records and site files Interpret data to identify protocol deviations and risks to subject safety data integrity. Only full time experience after obtaining essential qualification will be considered for the posts.

8. Job Responsibilities: Have to work in general medicine opd & ward. He/she will be required for coordinating with PI at study sites at headquarters, study monitoring, for collection of data and follow up of participants in the cohort. All the data recording, reporting and entries. Collection of the blood sample from patients and control subjects. All work assigned by PI for the project. This project may require calling the patient, helping or guiding them in the hospital and follow up for any events.