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Pharmacovigilance Process Manager

  • ... Posted on: Mar 24, 2026
  • ... Spectra force
  • ... Glenbrook Countryside, Illinois
  • ... Salary: Not Available
  • ... Full-time

Pharmacovigilance Process Manager   

Job Title :

Pharmacovigilance Process Manager

Job Type :

Full-time

Job Location :

Glenbrook Countryside Illinois United States

Remote :

No

Jobcon Logo Job Description :

Title: Pharmacovigilance Process Manager Location: Northbrook, IL 60062 Duration: 2 Years Rate: $60-64/hour Description Responsible for defining standards for PV process related matter and procedure in line with global PV process strategy. Development and maintenance of global standards and processes for case processing and related activities. Responsible to define standards for AE intake requirements. Continuously assess processes and identify opportunities to improve efficiency, effectiveness and compliance. Able to lead projects to the implementation of process improvements. Manage planned and unplanned deviations and ensure accurate periodic review. Assist with setting standards, decision making and maintenance of product specific case handling conventions in consultation with PV Process Management. Management for Argus system changes to ensure accurate and timely assessment of impact to global PV process. Liaison with PV functional teams (Medical Safety Science) for impact of process changes. Perform impact analysis for global regulatory intelligence results. Maintain standards and procedures for identification and management of Product Quality Complaints associated with safety information coordination with other PV functions and QA units related to triage, case processing, investigation, reconciliation and reporting. Assist PV Process as SME during audits and inspections. Requirements Minimum MSc in life sciences. Minimum of 7 years relevant experience in PV or combined PV/RA/QA and/or clinical development. Extensive PV knowledge. Strong interpersonal skills and multicultural awareness. Able to lead complex process improvement projects. Able to negotiate and build consensus for plans and priorities and develop effective relationships through collaboration. Able to make decisions and involves management at the right moment. Excellent oral and written communication skills in English, with an ability to interact with all levels of personnel, and global SMEs. Demonstrated ability to proactively predict and resolve complex problems, think strategically and tactically, generate solutions to complex problems and build consensus across global organization. Able to interpret, execute and recommend changes to established policies and programs. Leadership, decision making and negotiation skills. Strong analytical skills. Six Sigma or similar process improvement methodology knowledge a plus. Additional Information All your information will be kept confidential according to EEO guidelines. Job Location #J-18808-Ljbffr

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Jobcon Logo Position Details

Posted:

Mar 24, 2026

Reference Number:

14660_3A365F734B9E881184A36B6DE26C5404

Employment:

Full-time

Salary:

Not Available

City:

Glenbrook Countryside

Job Origin:

APPCAST_CPC

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Title: Pharmacovigilance Process Manager Location: Northbrook, IL 60062 Duration: 2 Years Rate: $60-64/hour Description Responsible for defining standards for PV process related matter and procedure in line with global PV process strategy. Development and maintenance of global standards and processes for case processing and related activities. Responsible to define standards for AE intake requirements. Continuously assess processes and identify opportunities to improve efficiency, effectiveness and compliance. Able to lead projects to the implementation of process improvements. Manage planned and unplanned deviations and ensure accurate periodic review. Assist with setting standards, decision making and maintenance of product specific case handling conventions in consultation with PV Process Management. Management for Argus system changes to ensure accurate and timely assessment of impact to global PV process. Liaison with PV functional teams (Medical Safety Science) for impact of process changes. Perform impact analysis for global regulatory intelligence results. Maintain standards and procedures for identification and management of Product Quality Complaints associated with safety information coordination with other PV functions and QA units related to triage, case processing, investigation, reconciliation and reporting. Assist PV Process as SME during audits and inspections. Requirements Minimum MSc in life sciences. Minimum of 7 years relevant experience in PV or combined PV/RA/QA and/or clinical development. Extensive PV knowledge. Strong interpersonal skills and multicultural awareness. Able to lead complex process improvement projects. Able to negotiate and build consensus for plans and priorities and develop effective relationships through collaboration. Able to make decisions and involves management at the right moment. Excellent oral and written communication skills in English, with an ability to interact with all levels of personnel, and global SMEs. Demonstrated ability to proactively predict and resolve complex problems, think strategically and tactically, generate solutions to complex problems and build consensus across global organization. Able to interpret, execute and recommend changes to established policies and programs. Leadership, decision making and negotiation skills. Strong analytical skills. Six Sigma or similar process improvement methodology knowledge a plus. Additional Information All your information will be kept confidential according to EEO guidelines. Job Location #J-18808-Ljbffr

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