Chetankumar Patel

FAQ About Chetankumar Patel

• What is Chetankumar Patel's address?

  Chetankumar Patel is located at
  Mumbai, Mumbai, India

• What is Chetankumar Patel's job title?

  Chetankumar Patel is a
  1.Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals. 2.Ensure that IRB approval of protocol and informed consent form is obtained prior to initiation of the study. 3.Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol. 4.Maintain Study Master File. 5.Confer with subject and to explain purpose of study. 6.Explain diagnostic procedures and method of treatment to answer subject and family concerns. 7.Obtain written consent for subject to participate in a study prior to initiation of any protocol procedures. 8.Maintain accurate records of the receipt, inventory, and dispensation of study drug and materials. 9.Work with the nursing staff to administer study drug to research subjects. 10.Obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol. 11.Assist in the development of consent forms; case report forms CRFs and source document templates as necessary. 12.Collect relevant information and data from subject charts and records, subject interviews, and other sources. 13.Complete case report forms eCRFs CRFs in accordance with research protocol guidelines. 14.Inspect eCRFs CRFs, source documentation, and study files to ensure completeness. 15.Review eCRFs CRFs, source documentation, and study files with representative Monitor from CRO Sponsor, at each Monitoring visit. 16.Make necessary corrections to eCRFs CRFs and submit requested documentation in a timely manner. 17.Comply with standard operating procedures of the sponsor, institutional review board IRB, and CRO involved with the trial. 18.Compile and submit reports, as necessary to the IRB, sponsor. 19.Reimbursement to patients and from the Sponsor. Specialties: Oncology Clinical Trials Iqvia

• What industry does Chetankumar Patel currently work in?

  Chetankumar Patel currently works in the
  Iqvia

• What is Chetankumar Patel's area of expertise?

  Chetankumar Patel specializes in
  1.Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals. 2.Ensure that IRB approval of protocol and informed consent form is obtained prior to initiation of the study. 3.Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol. 4.Maintain Study Master File. 5.Confer with subject and to explain purpose of study. 6.Explain diagnostic procedures and method of treatment to answer subject and family concerns. 7.Obtain written consent for subject to participate in a study prior to initiation of any protocol procedures. 8.Maintain accurate records of the receipt, inventory, and dispensation of study drug and materials. 9.Work with the nursing staff to administer study drug to research subjects. 10.Obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol. 11.Assist in the development of consent forms; case report forms CRFs and source document templates as necessary. 12.Collect relevant information and data from subject charts and records, subject interviews, and other sources. 13.Complete case report forms eCRFs CRFs in accordance with research protocol guidelines. 14.Inspect eCRFs CRFs, source documentation, and study files to ensure completeness. 15.Review eCRFs CRFs, source documentation, and study files with representative Monitor from CRO Sponsor, at each Monitoring visit. 16.Make necessary corrections to eCRFs CRFs and submit requested documentation in a timely manner. 17.Comply with standard operating procedures of the sponsor, institutional review board IRB, and CRO involved with the trial. 18.Compile and submit reports, as necessary to the IRB, sponsor. 19.Reimbursement to patients and from the Sponsor. Specialties: Oncology Clinical Trials

• Which languages does Chetankumar Patel speak? 

  Chetankumar Patel speaks the following languages:
  No languages available.

• Which industries has Chetankumar Patel previously worked in?   

  Chetankumar Patel has prior experience in the following industries:
  Iqvia , Iqvia , Iqvia , Sahajanand Life Sciences , Piramal Enterprises , Cipla , Tata Memorial Centre

• What is Chetankumar Patel’s work experience?  

  Chetankumar Patel has the following professional experience:
  Iqvia , Iqvia , Iqvia , Iqvia , Sahajanand Life Sciences , Piramal Enterprises , Cipla , Tata Memorial Centre .

• How can I find Chetankumar Patel on LinkedIn?  

  You can view Chetankumar Patel’s
  LinkedIn profile at LinkedIn URL.

• What are Chetankumar Patel’s work email addresses?  

  Chetankumar Patel’s work email addresses are
  [email protected] .

• What company does Chetankumar Patel work for?  

  Chetankumar Patel works at
  Iqvia