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Affiliate Safety Representative

AbbVie

Affiliate Safety Representative

AbbVie

Dublin

·

On-site

·

Full-time

·

1w ago

Benefits & Perks

Healthcare

401k

Unlimited Pto

Required Skills

Pharmacovigilance

Regulatory Compliance

Communication

Scientific knowledge

Risk Management

Quality management

Adverse event reporting

The Affiliate Safety Representative (ASR) is responsible for ensuring that all aspects of Pharmacovigilance (PV) within the Affiliate meet Abb Vie’s statutory and ethical standards, and comply with local and regional PV regulations for the product portfolio. The ASR acts as the Affiliate’s Lead for PV matters with the National Regulatory Agency and Abb Vie Global Patient Safety (GPS) PSEQ function.

Key Responsibilities:

  • Oversight of the local Pharmacovigilance System to ensure compliance with Abb Vie Global procedures and relevant regulations.

  • Collaborate with Regional PV Teams and partners to monitor PV activities and performance.

  • Partner to maintain Quality Management Systems and oversee PV training compliance.

  • Ensure robust systems for Adverse Event and Periodic Safety Reporting across spontaneous, solicited, and clinical study sources.

  • Serve as Affiliate lead during Regulatory Authority PV inspections and internal audits.

  • Advise cross-functional partners on PV requirements, safety information handling, and PV agreements.

  • Support PV training and educational initiatives for local teams and partners.

  • Monitor legislation intelligence and assess impacts on PV systems.

  • Lead local risk management activities, including Risk Management Plans and implementation of risk minimisation measures.

  • Maintain awareness of safety profiles and emerging concerns for Abb Vie products within the jurisdiction.

  • Drive PV advocacy and participate in internal and external collaborations with stakeholders and agencies.

  • Ensure preparedness for after-hours availability and business continuity through PV Disaster Recovery Plans.

  • BSc, MPharm, or PhD in a scientific discipline (preferred)

  • Minimum two years' experience in the pharmaceutical industry in a pharmacovigilance role

  • Excellent written and verbal communication and presentation skills

  • Fluency in English

  • High customer orientation and commitment to compliance and scientific integrity

  • Strong scientific acumen, judgment, planning, and organisational skills; demonstrated sense of urgency

Stakeholders:

  • Internal: Medical, Regulatory Affairs, Clinical, Quality Assurance, Customer Service, Marketing, Sales, Operations, Patient Experience, Customer Excellence, General Manager
  • External: National Regulatory Agency, GPS (Regional PV Team, QPPV Office, Risk Management Teams), healthcare practitioners, consumers, and patients

Ready to shape the future of patient safety at Abb Vie? Apply now and bring your pharmacovigilance expertise to our passionate team—make an impact where it truly matters!

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

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About AbbVie

AbbVie

AbbVie

Public

Pharmaceutical company.

10,001+

Employees

North Chicago

Headquarters

Reviews

3.7

1 reviews

Work Life Balance

3.0

Compensation

3.0

Culture

3.0

Career

3.5

Management

2.5

60%

Recommend to a Friend

Pros

Good resume experience for entry-level positions

Valuable work experience opportunity

Brand recognition benefits

Cons

Lack of explicit feedback on performance

Limited communication about role expectations

No clear guidance provided

Salary Ranges

88 data points

Junior/L3

Mid/L4

Intern

Director

Junior/L3 · Associate Business Systems Consultant

4 reports

$167,325

total / year

Base

$145,500

Stock

-

Bonus

-

$141,860

$170,567

Interview Experience

6 interviews

Difficulty

2.8

/ 5

Duration

14-28 weeks

Offer Rate

17%

Experience

Positive 0%

Neutral 33%

Negative 67%

Interview Process

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Panel Interview

5

Final Interview

6

Offer

Common Questions

Behavioral/STAR

Past Experience

Technical Knowledge

Culture Fit