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PHARMA JOBS POST > Bangalore > Alcon job vacancy for Patient Safety Monitor – Apply Now
BangaloreClinical ResearchClinical Research AssociateClinical Research Coordinator

Alcon job vacancy for Patient Safety Monitor – Apply Now

ADMIN
Last updated: October 3, 2023 12:05 pm
ADMIN 3 years ago
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Alcon job vacancy for Patient Safety Monitor – Apply Now

Patient Safety Monitor

Bangalore, India

Major Accountabilities (Describe the main results of the job to be achieved )

Case Processing:

Process case files according to Standard Operating Procedures (SOP).
Work with affiliate offices to ensure required dataset has been received/requested.
Re-assess the data, ensure accurate product selection and assign required event code(s) in the system.
Complete initial and follow-up reporting assessments as information is received (initial report, follow-up questionnaires, phone calls, investigation findings).
Respond to Manufacturing Quality Assurance (QA) requests and Health Authority inquiries
Launch required quality investigation records.
Schedule expedited and periodic regulatory reports based on local and international reporting regulations.
Perform and receive quality feedback on case management and coding.
Adherence to all corporate compliance guidelines & corporate programs.
Maintains a working knowledge of the following:

Alcon Products for assigned therapeutic areas and corresponding documentation (Product Information, Directions for Use, Manuals, Promotional materials)
Eye anatomy
Common diseases
Ophthalmic evaluation procedures
Eye terminology and abbreviations
Safety database(s) and reporting tools
Process and review Surgical – Intra Ocular Lens (IOL) complaint records in accordance with Alcon Standard Operating Procedures (SOPs)
Provide support in reconciliation activities and audit as required.
Evaluate and escalate potential safety issues to management.

Key Performance Indicators (Indicate how performance will be measured: indicators, activities…)

KPIs will be outlined in detail in the goal sheet, and will largely be around below parameters:

Meets internal and external quality standards
Review and close files within prescribed timelines
Creates high quality regulatory reports for submission on or before assigned due dates

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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