About the Company:
IQVIA is a main worldwide supplier of cutting edge investigation, innovation arrangements and clinical exploration administrations to the existence sciences industry. We trust in pushing the limits of human science and information science to have the greatest effect conceivable - to assist our clients with making a better world. Learn more at our site.
About the Job:
Experience: 3-5 years of graduation and need to have relevant experience
Capable in Microsoft Office programming, including Word and Succeed.
• Capable in electronic information the executives programming.
• Capacity to audit, support, and distribute electronic records. Magnificent English composed and verbal relational abilities.
• Positive association abilities, scrupulousness, and authoritative abilities.
• Capacity to deal with different undertakings and to completely finish culmination of alloted errands with some management.
• Great critical thinking abilities.
• Capacity to lay out and keep up with powerful working associations with colleagues, administrators and clients.
• Familiarity with fundamental GxP necessities. Capacity to learn logical, clinical, and administrative phrasing to acquire a comprehension of Value information and fields in QA database(s) to have the option to decipher information client demands for data into explicit questions expected to produce mentioned measurements autonomously.
• May partake in review direct.
Fundamental Capabilities
- Site Review and Investigation CAPA audit the board for relegated accounts
- Concentrated support:Audits and Reviews discoveries arrangement and CAPA endorsements inside eQMS as help to Lead QA
- Produce measurements and follow up consistently as material for Quality occasions
- Produce documentation from the QA information bases, including status reports as
required.
- Keeps up with the QA database(s) guaranteeing Reviews when distinguished are placed onto the framework from review plans/warning documentation and that the framework is refreshed as required.
- Review data is followed up as expected, through the full review life cycle including: Missing Data connecting with the arranged reviews are distinguished, accumulated and entered. Performed reviews are affirmed. The full text of review discoveries are placed onto the information base from Support/Administrative review reports. - - Follow-up of Reports and Remedial And Preventive Activities and Follow-up of late Basic/Significant discoveries. Declarations and contracted review documentation are given and conveyed as suitable.
- Offer help to staff by noting more complicated inquiries concerning the utilization of EDA
- Partake in the turn of events and give preparing on new/improved QA data set upkeep processes including giving preparation to new clients engaged with QA data set support .Keep current in propels in subject matter, including administrative information, patterns, and advancements, incorporating consenting to every single required Sop and timetables
- Following up and Shutting reviews/Examination Restorative and preventive activities (CAPA) in the eQMS.
Openings for Clinical data management in TCS
Experience: 1-10 years
Qualification : BSc/ MSc/ M. Pharma or Pharm D
Location of the Job: Pune/ Hyderabad/ Bangalore/ Mumbai/ Chennai
Send resumes to [email protected]