LS - Pharma-Consultant
Kolkata
HEALTHCARE LIFESCIENCES SERVICES
Experience : >10 YEARS
Job Code : 1153808
Apply Now We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristic protected by law.

Wipro does not charge any fee at any stage of the recruitment process and has not authorised agencies/partners to collect any fee for recruitment. If you encounter any suspicious mail, advertisements or persons who offer jobs at Wipro, please do let us know by contacting us on helpdesk.recruitment@wipro.com
We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristic protected by law. Wipro does not charge any fee at any stage of the recruitment process and has not authorised agencies/partners to collect any fee for recruitment. If you encounter any suspicious mail, advertisements or persons who offer jobs at Wipro, please do let us know by contacting us on helpdesk.recruitment@wipro.com

Mandatory Skills:

LS - Pharma-L3

Job Description:

Responsibilities: Understanding of clinical documents (Safety , Submission and R& D related documents) Set up, implement and maintain an eTMF (Trial Master File) in accordance with the DIA reference model  Oversight of compliance alongside quality functions and data privacy requirements Ensure the completeness of the Trial Master File (TMF) for assigned clinical studies Identification and categorizing of clinical trial documents Quality checking of documents for legibility, duplicity and completeness Identification of various properties and features of clinical documents  Provide support to Clinical Document QC Specialist with regards to ICH/GCP documentationWorking Experience / Skill set in: Clinical document management system Clinical research monitoring, pharmaceutical, CRO or healthcare industry Knowledge of ICH GCP, 21 CFR part11 Working knowledge of clinical essential documents, including trial master file Relevant clinical research experience in industry or in clinical practice as a trial/study coordinator

Roles & Responsibilities:

Minimum Experience Required:
Mandatory Skills: LS - Pharma-L3 Consulting-L2
Desirable Skills:
Language Skills: English Language-L2

Apply Now We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristic protected by law.

Wipro does not charge any fee at any stage of the recruitment process and has not authorised agencies/partners to collect any fee for recruitment. If you encounter any suspicious mail, advertisements or persons who offer jobs at Wipro, please do let us know by contacting us on helpdesk.recruitment@wipro.com
We are an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristic protected by law. Wipro does not charge any fee at any stage of the recruitment process and has not authorised agencies/partners to collect any fee for recruitment. If you encounter any suspicious mail, advertisements or persons who offer jobs at Wipro, please do let us know by contacting us on helpdesk.recruitment@wipro.com