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Cliantha Research

 

Cliantha Research Recruitment for Officer/Sr.Officer-Consumer Research

Cliantha Research Limited Recruitment 2021. Cliantha Research Limited Notification full detailes 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.
  1. Post Name: Officer/Sr.Officer-Consumer Research
  2. Education:B.Pharm / D.Pharm / M.Sc/B.sc
  3. Experienced:2 to 4 years
  4. Location:Ahmedabad
  5. Salary: NA
  6. Openings:NA

Note:If interested candidates can share your resume to mentioned mail ID Below

apurohit@cliantha.com

 Job Description: Hiring For Officer/Sr.Officer-Consumer Research in Cliantha Research Limited!  If interested candidates can share your resume to mentioned mail ID

apurohit@cliantha.com

1. Ensure that EC approved protocol is available prior to commencement of thestudy.
2. Ensure about the prearrangement of study requirements (i.e. requisition ofrandomization schedule, meals requisition, test product availability etc.)
3. Follow the proposed timelines for conducting and completing the clinicaltrials.
4. Place a requisition to Quality Control (QC) for requisite number of forms(General forms and Study specific forms) well in advance as required for the study.
5. Initiate the preparation of Trial Master File for respective study.
6. Inform the Sponsor and EC of any changes to the protocol or safety concernsand submit progress reports to the EC per requirements.
7. Place a pre-study meeting request for study staff training on most recent ECapproved protocol and delegation of duties by the study staff in consultationwith PI.
8. Update the staff, CRM and Team lead on study progress plan.
9. Manage study supplies (Lab kits, CRFs, clinical supplies, etc.) and meals of study subjects in timely manner.
10. Ensure timely review of study data.
11. Coordinate study-monitoring visits and conduct subject visits according torequirements.
12. Work in coordination with Quality Control to ensure all corrections have been made during and after the study conduct.
13. Report required Adverse Events or Serious Adverse Events to PI/ Sub I/ CRM.
14. Ensure Adverse Events reporting is documented (e.g., Serious, Severe,Moderate, Mild, Expected, Unexpected).
15. Be a protector of study documents and responsible for accountability andappropriate usage of study forms.
16. Investigational Products/Test products receipt, storage, accountabilities,disposal, return and archiving.
17. Willing to work in shifts.
18. Ensure to follow and adherence of organization’s general rules and applicable policies.
19. Any additional 

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and Apply Online

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