Opening for freshers as Pharmacovigilance Specialist @ Baxter
Baxter International Inc., through its subsidiaries, develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Baxter had 2012 sales of $14.2 billion and has approximately 50,800 employees.
Baxter India is a wholly owned subsidiary of Baxter International Inc. Baxter India believes in engaging collaboratively with patients, healthcare providers, governments and non - government organizations to help change the lives of millions of people by providing safe, effective and affordable products and therapies.
Job Title : PV (pharmacovigilance) Specialist
Job Description : AE/SAE Processing
To collect, process and follow up all local adverse events (AEs)/ serious adverse events (SAEs) from different sources (RHC call center, Healthcare professionals, sales and marketing personnel, patients, clinical trials, etc.);
To report the AE/SAE to the HA according to the India regulation (Schedule Y) within the required timeframe;
To log in cases into the local tracking system and transmit all reports in English to the GPV organization within the required timeframe;
To archive all source documentation in accordance with Quality Control;
To file all Pharmacovigilance source documents and keep them available upon request by the HA.
CIOMS Form Collecting :
To maintain the Baxter PSS data base;
To collect CIOMS form from GPV within the required timeframe.
Document Archiving
To maintain and archive the signed training record;
To maintain and archive the hardcopy of package insert;
To archive the PV related communication and correspondence
Desired Profile :
Educational Qualifications : Clinical Medicine, Pharmacy or Science background, bachelor or above;
Experience :
At least 1 year relevant working experiences in pharmaceutical company;
Knowledge of the relevant PV regulations in India
Good communication skills, ability to liaise with the different function involved: QA, RA, MA, marketing and sales team, etc.;
Fluent in English both in oral & written.
How to Apply :
Interested candidates can apply by sending their updated resume to jobs@baxter.com
Baxter International Inc., through its subsidiaries, develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Baxter had 2012 sales of $14.2 billion and has approximately 50,800 employees.
Baxter India is a wholly owned subsidiary of Baxter International Inc. Baxter India believes in engaging collaboratively with patients, healthcare providers, governments and non - government organizations to help change the lives of millions of people by providing safe, effective and affordable products and therapies.
Job Title : PV (pharmacovigilance) Specialist
Job Description : AE/SAE Processing
To collect, process and follow up all local adverse events (AEs)/ serious adverse events (SAEs) from different sources (RHC call center, Healthcare professionals, sales and marketing personnel, patients, clinical trials, etc.);
To report the AE/SAE to the HA according to the India regulation (Schedule Y) within the required timeframe;
To log in cases into the local tracking system and transmit all reports in English to the GPV organization within the required timeframe;
To archive all source documentation in accordance with Quality Control;
To file all Pharmacovigilance source documents and keep them available upon request by the HA.
CIOMS Form Collecting :
To maintain the Baxter PSS data base;
To collect CIOMS form from GPV within the required timeframe.
Document Archiving
To maintain and archive the signed training record;
To maintain and archive the hardcopy of package insert;
To archive the PV related communication and correspondence
Desired Profile :
Educational Qualifications : Clinical Medicine, Pharmacy or Science background, bachelor or above;
Experience :
At least 1 year relevant working experiences in pharmaceutical company;
Knowledge of the relevant PV regulations in India
Good communication skills, ability to liaise with the different function involved: QA, RA, MA, marketing and sales team, etc.;
Fluent in English both in oral & written.
How to Apply :
Interested candidates can apply by sending their updated resume to jobs@baxter.com
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