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Spanish speaking Affiliate Pharmacovigilance Associate

Cognizant

Healthcare Jobs

Spanish speaking Affiliate Pharmacovigilance Associate

full-timePosted: Dec 6, 2025

Job Description

Spanish speaking Affiliate Pharmacovigilance Associate

Employment Type: Full-time
Location: Budapest
Shift Pattern: General
Work From Office (WFO): We currently work from the office 2 days per month. This arrangement is flexible and may change to 1–2 days per week based on HR communication.

We offer:

· Competitive salary and benefit package (cafeteria + annual bonus)

· Training and continuous learning and certification opportunities

· Free medical benefit package

· Reimbursable language courses

· Risk and accident insurance

· Chance to be part of a rapidly expanding organization

· Multilingual, multicultural environment with native colleagues

· All You Can Move SportPass (at a discounted price)

· Team events, company events

· Relocation package

· High value awards and recognitions

Your profile:

  • Graduate in Pharmacy or Life Science
  • 1 year of Pharmacovigilance or relevant clinical experience
  • Min. B2 spoken and written Spanish and English proficiency

Key Responsibilities:

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.
  • Monitoring mailbox, triage for patient safety reports and emails.
  • Maintaining and archival of emails/source documents and updating shared folders.
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information.
  • Obtain consent from reporter to follow up on safety reports.
  • Assess cases for missing information and follow up attempts until closure.
  • Check case validity.
  • Perform initial checks, search database to prevent duplicate entries.
  • Ensure upfront clarification requests in case of data discrepancy identified in source document.
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge.
  • Translation & Back Translation of safety information as applicable.
  • Anonymize/redact source documents and/or AE forms (as applicable).
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information.
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV.
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports.
  • Document review processes.
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines.
  • Work with project quality roles to improve case quality.
  • Attend training sessions and develop skills and capabilities on an ongoing basis.
  • Timely completion of assigned trainings and training files.
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations.
  • Assists in the training and mentorship of new joiners as necessary.

The Cognizant community:
We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive.

  • Cognizant is a global community with more than 300,000 associates around the world.
  • We don’t just dream of a better way – we make it happen.
  • We take care of our people, clients, company, communities and climate by doing what’s right.
  • We foster an innovative environment where you can build the career path that’s right for you.

About us:
Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com

Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email CareersNA2@cognizant.com with your request and contact information.

Disclaimer:
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.

Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.

About the Role/Company

  • Cognizant is a global community with more than 300,000 associates around the world
  • We don’t just dream of a better way – we make it happen
  • We take care of our people, clients, company, communities and climate by doing what’s right
  • Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era
  • Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses
  • Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world
  • Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws

Key Responsibilities

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable
  • Monitoring mailbox, triage for patient safety reports and emails
  • Maintaining and archival of emails/source documents and updating shared folders
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information
  • Obtain consent from reporter to follow up on safety reports
  • Assess cases for missing information and follow up attempts until closure
  • Check case validity
  • Perform initial checks, search database to prevent duplicate entries
  • Ensure upfront clarification requests in case of data discrepancy identified in source document
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge
  • Translation & Back Translation of safety information as applicable
  • Anonymize/redact source documents and/or AE forms (as applicable)
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports
  • Document review processes
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines
  • Work with project quality roles to improve case quality
  • Attend training sessions and develop skills and capabilities on an ongoing basis
  • Timely completion of assigned trainings and training files
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations
  • Assists in the training and mentorship of new joiners as necessary

Required Qualifications

  • Graduate in Pharmacy or Life Science
  • year of Pharmacovigilance or relevant clinical experience
  • Min. B2 spoken and written Spanish and English proficiency

Skills Required

  • Spanish language proficiency (B2 level)
  • English language proficiency (B2 level)
  • Pharmacovigilance or relevant clinical experience

Benefits & Perks

  • Competitive salary and benefit package (cafeteria + annual bonus)
  • Training and continuous learning and certification opportunities
  • Free medical benefit package
  • Reimbursable language courses
  • Risk and accident insurance
  • Chance to be part of a rapidly expanding organization
  • Multilingual, multicultural environment with native colleagues
  • All You Can Move SportPass (at a discounted price)
  • Team events, company events
  • Relocation package
  • High value awards and recognitions

Additional Requirements

  • Employment Type: Full-time
  • Location: Budapest
  • Shift Pattern: General
  • Work From Office (WFO): We currently work from the office 2 days per month. This arrangement is flexible and may change to 1–2 days per week based on HR communication

Locations

  • India

Salary

Estimated Salary Rangemedium confidence

800,000 - 1,500,000 INR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Spanish language proficiency (B2 level)intermediate
  • English language proficiency (B2 level)intermediate
  • Pharmacovigilance or relevant clinical experienceintermediate

Required Qualifications

  • Graduate in Pharmacy or Life Science (experience)
  • year of Pharmacovigilance or relevant clinical experience (experience)
  • Min. B2 spoken and written Spanish and English proficiency (experience)

Responsibilities

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable
  • Monitoring mailbox, triage for patient safety reports and emails
  • Maintaining and archival of emails/source documents and updating shared folders
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information
  • Obtain consent from reporter to follow up on safety reports
  • Assess cases for missing information and follow up attempts until closure
  • Check case validity
  • Perform initial checks, search database to prevent duplicate entries
  • Ensure upfront clarification requests in case of data discrepancy identified in source document
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge
  • Translation & Back Translation of safety information as applicable
  • Anonymize/redact source documents and/or AE forms (as applicable)
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports
  • Document review processes
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines
  • Work with project quality roles to improve case quality
  • Attend training sessions and develop skills and capabilities on an ongoing basis
  • Timely completion of assigned trainings and training files
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations
  • Assists in the training and mentorship of new joiners as necessary

Benefits

  • general: Competitive salary and benefit package (cafeteria + annual bonus)
  • general: Training and continuous learning and certification opportunities
  • general: Free medical benefit package
  • general: Reimbursable language courses
  • general: Risk and accident insurance
  • general: Chance to be part of a rapidly expanding organization
  • general: Multilingual, multicultural environment with native colleagues
  • general: All You Can Move SportPass (at a discounted price)
  • general: Team events, company events
  • general: Relocation package
  • general: High value awards and recognitions

Target Your Resume for "Spanish speaking Affiliate Pharmacovigilance Associate" , Cognizant

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Check Your ATS Score for "Spanish speaking Affiliate Pharmacovigilance Associate" , Cognizant

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Keyword optimization analysis
Skill matching & gap identification
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Cognizant logo

Spanish speaking Affiliate Pharmacovigilance Associate

Cognizant

Healthcare Jobs

Spanish speaking Affiliate Pharmacovigilance Associate

full-timePosted: Dec 6, 2025

Job Description

Spanish speaking Affiliate Pharmacovigilance Associate

Employment Type: Full-time
Location: Budapest
Shift Pattern: General
Work From Office (WFO): We currently work from the office 2 days per month. This arrangement is flexible and may change to 1–2 days per week based on HR communication.

We offer:

· Competitive salary and benefit package (cafeteria + annual bonus)

· Training and continuous learning and certification opportunities

· Free medical benefit package

· Reimbursable language courses

· Risk and accident insurance

· Chance to be part of a rapidly expanding organization

· Multilingual, multicultural environment with native colleagues

· All You Can Move SportPass (at a discounted price)

· Team events, company events

· Relocation package

· High value awards and recognitions

Your profile:

  • Graduate in Pharmacy or Life Science
  • 1 year of Pharmacovigilance or relevant clinical experience
  • Min. B2 spoken and written Spanish and English proficiency

Key Responsibilities:

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.
  • Monitoring mailbox, triage for patient safety reports and emails.
  • Maintaining and archival of emails/source documents and updating shared folders.
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information.
  • Obtain consent from reporter to follow up on safety reports.
  • Assess cases for missing information and follow up attempts until closure.
  • Check case validity.
  • Perform initial checks, search database to prevent duplicate entries.
  • Ensure upfront clarification requests in case of data discrepancy identified in source document.
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge.
  • Translation & Back Translation of safety information as applicable.
  • Anonymize/redact source documents and/or AE forms (as applicable).
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information.
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV.
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports.
  • Document review processes.
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines.
  • Work with project quality roles to improve case quality.
  • Attend training sessions and develop skills and capabilities on an ongoing basis.
  • Timely completion of assigned trainings and training files.
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations.
  • Assists in the training and mentorship of new joiners as necessary.

The Cognizant community:
We are a high caliber team who appreciate and support one another. Our people uphold an energetic, collaborative and inclusive workplace where everyone can thrive.

  • Cognizant is a global community with more than 300,000 associates around the world.
  • We don’t just dream of a better way – we make it happen.
  • We take care of our people, clients, company, communities and climate by doing what’s right.
  • We foster an innovative environment where you can build the career path that’s right for you.

About us:
Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com

Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email CareersNA2@cognizant.com with your request and contact information.

Disclaimer:
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.

Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.

About the Role/Company

  • Cognizant is a global community with more than 300,000 associates around the world
  • We don’t just dream of a better way – we make it happen
  • We take care of our people, clients, company, communities and climate by doing what’s right
  • Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era
  • Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses
  • Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2025) is consistently listed among the most admired companies in the world
  • Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws

Key Responsibilities

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable
  • Monitoring mailbox, triage for patient safety reports and emails
  • Maintaining and archival of emails/source documents and updating shared folders
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information
  • Obtain consent from reporter to follow up on safety reports
  • Assess cases for missing information and follow up attempts until closure
  • Check case validity
  • Perform initial checks, search database to prevent duplicate entries
  • Ensure upfront clarification requests in case of data discrepancy identified in source document
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge
  • Translation & Back Translation of safety information as applicable
  • Anonymize/redact source documents and/or AE forms (as applicable)
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports
  • Document review processes
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines
  • Work with project quality roles to improve case quality
  • Attend training sessions and develop skills and capabilities on an ongoing basis
  • Timely completion of assigned trainings and training files
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations
  • Assists in the training and mentorship of new joiners as necessary

Required Qualifications

  • Graduate in Pharmacy or Life Science
  • year of Pharmacovigilance or relevant clinical experience
  • Min. B2 spoken and written Spanish and English proficiency

Skills Required

  • Spanish language proficiency (B2 level)
  • English language proficiency (B2 level)
  • Pharmacovigilance or relevant clinical experience

Benefits & Perks

  • Competitive salary and benefit package (cafeteria + annual bonus)
  • Training and continuous learning and certification opportunities
  • Free medical benefit package
  • Reimbursable language courses
  • Risk and accident insurance
  • Chance to be part of a rapidly expanding organization
  • Multilingual, multicultural environment with native colleagues
  • All You Can Move SportPass (at a discounted price)
  • Team events, company events
  • Relocation package
  • High value awards and recognitions

Additional Requirements

  • Employment Type: Full-time
  • Location: Budapest
  • Shift Pattern: General
  • Work From Office (WFO): We currently work from the office 2 days per month. This arrangement is flexible and may change to 1–2 days per week based on HR communication

Locations

  • India

Salary

Estimated Salary Rangemedium confidence

800,000 - 1,500,000 INR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Spanish language proficiency (B2 level)intermediate
  • English language proficiency (B2 level)intermediate
  • Pharmacovigilance or relevant clinical experienceintermediate

Required Qualifications

  • Graduate in Pharmacy or Life Science (experience)
  • year of Pharmacovigilance or relevant clinical experience (experience)
  • Min. B2 spoken and written Spanish and English proficiency (experience)

Responsibilities

  • Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information
  • Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable
  • Monitoring mailbox, triage for patient safety reports and emails
  • Maintaining and archival of emails/source documents and updating shared folders
  • Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information
  • Obtain consent from reporter to follow up on safety reports
  • Assess cases for missing information and follow up attempts until closure
  • Check case validity
  • Perform initial checks, search database to prevent duplicate entries
  • Ensure upfront clarification requests in case of data discrepancy identified in source document
  • Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge
  • Translation & Back Translation of safety information as applicable
  • Anonymize/redact source documents and/or AE forms (as applicable)
  • Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information
  • Identify discrepancies and maintain email clarifications of discrepancies for SDV
  • Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports
  • Document review processes
  • Responsible for completion of day-to-day work and process flows within the agreed SLAs
  • Maintaining data as per customer guidelines
  • Work with project quality roles to improve case quality
  • Attend training sessions and develop skills and capabilities on an ongoing basis
  • Timely completion of assigned trainings and training files
  • Co-ordinate with internal teams to obtain necessary information required for day-to-day operations
  • Assists in the training and mentorship of new joiners as necessary

Benefits

  • general: Competitive salary and benefit package (cafeteria + annual bonus)
  • general: Training and continuous learning and certification opportunities
  • general: Free medical benefit package
  • general: Reimbursable language courses
  • general: Risk and accident insurance
  • general: Chance to be part of a rapidly expanding organization
  • general: Multilingual, multicultural environment with native colleagues
  • general: All You Can Move SportPass (at a discounted price)
  • general: Team events, company events
  • general: Relocation package
  • general: High value awards and recognitions

Target Your Resume for "Spanish speaking Affiliate Pharmacovigilance Associate" , Cognizant

Get personalized recommendations to optimize your resume specifically for Spanish speaking Affiliate Pharmacovigilance Associate. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Spanish speaking Affiliate Pharmacovigilance Associate" , Cognizant

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

TechnologyIT ServicesTechnologyConsulting

Answer 10 quick questions to check your fit for Spanish speaking Affiliate Pharmacovigilance Associate @ Cognizant.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.