Amit Kumar Email & Phone Number | Experienced clinical research professional with proven track record of success in progressively responsible, having over 10 years’ experience in clinical research, and has demonstrated great expertise in both monitoring, clinical operations activities & documentation process within multinational studies (phase II, III and Phase IV). I am Bachelor in Bio-technology with Advanced Post-Graduate Diploma in clinical research. Having extensive knowledge of ICH- GCP, FDA regulations. Experience in study Investigator recruitment and monitoring multiple site locations. Experience of conducting more than 120+on-site monitoring visits for Phase II-IV clinical studies. Site management, relationship building, strategic decision making, strong presentation skills, and training research staff. Brief understanding and Good Knowledge of. 1. Clinical Trial Process. 2. ICH GCP. 3. INDIAN GCP. 4. Schedule-Y Guidelines. 5. 21st CFR. 6. US-FDA Regulations. 7. Good Knowledge of PSMT, QSMT, SSMT Documentation, GDP. 8. ICMR Guidelines. 9. Clinical Trial Documentation and Monitoring Process. 10. Clinical Trial Protocol. 11. Standard Operating Process. 12. Records Management & Document Process. 13. Communication, Presentation and Management Skills. 14. Clinical Trial Budget. 15. Preparing trial sites for sponsor audit and regulatory inspection."

Amit Kumar

Experienced clinical research professional with proven track record of success in progressively resp...
India

*50 free lookup(s) per month.

Amit Kumar’s Email rajdebagill@yahoo.in

Amit Kumar’s Phone Numbers

Get AMIT’s Phone Number (For Free)

Social Media

Amit Kumar’s Location India

Amit Kumar’s Current Industry Iqvia

Amit Kumar’s Prior Industry National Institute Of Tuberculosis And Respiratory Diseases | Max Neeman International | Dr Lal Pathlabs

Find accurate emails & phone numbers for over 700M professionals.

Functional Centralized Monitoring Lead

2023-03-01 00:00:00 - Present

Research Assistant

2012-09-01 00:00:00 - 2016-05-01 00:00:00

Clinical Research Coordinator/Clinical Research Associate

2011-04-01 00:00:00 - 2012-09-01 00:00:00

Phlebotomist/Lab Assistant

2009-10-01 00:00:00 - 2011-01-01 00:00:00

No Skills Available

No Languages Available

Amit Kumar is a Experienced clinical research professional with proven track record of success in progressively responsible, having over 10 years’ experience in clinical research, and has demonstrated great expertise in both monitoring, clinical operations activities & documentation process within multinational studies (phase II, III and Phase IV). I am Bachelor in Bio-technology with Advanced Post-Graduate Diploma in clinical research. Having extensive knowledge of ICH- GCP, FDA regulations. Experience in study Investigator recruitment and monitoring multiple site locations. Experience of conducting more than 120+on-site monitoring visits for Phase II-IV clinical studies. Site management, relationship building, strategic decision making, strong presentation skills, and training research staff. Brief understanding and Good Knowledge of. 1. Clinical Trial Process. 2. ICH GCP. 3. INDIAN GCP. 4. Schedule-Y Guidelines. 5. 21st CFR. 6. US-FDA Regulations. 7. Good Knowledge of PSMT, QSMT, SSMT Documentation, GDP. 8. ICMR Guidelines. 9. Clinical Trial Documentation and Monitoring Process. 10. Clinical Trial Protocol. 11. Standard Operating Process. 12. Records Management & Document Process. 13. Communication, Presentation and Management Skills. 14. Clinical Trial Budget. 15. Preparing trial sites for sponsor audit and regulatory inspection."

Amit Kumar has prior
experience in the following industries:
National Institute Of Tuberculosis And Respiratory Diseases | Max Neeman International | Dr Lal Pathlabs

Amit Kumar has the following professional experience:
Iqvia | National Institute Of Tuberculosis And Respiratory Diseases | Max Neeman International | Dr Lal Pathlabs