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Safety Surveillance Associate Jobs (NOW HIRING)

Alexion Pharmaceuticals, Inc.

The Associate Director, Safety Scientist plays a pivotal role within Global Patient Safety ... Leading program and study level safety surveillance including the analysis and communication of ...

CRISPR Therapeutics

Oversee medical aspects of long‑term follow‑up (LTFU) safety surveillance, including ... Base Pay Associate Director, Medical Safety: Base pay range of $170,000 to $190,000+ bonus, equity ...

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Safety Surveillance Associate information

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$14

$26

$45

How much do safety surveillance associate jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for safety surveillance associate in the United States is $26.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $33.65 per hour, depending on experience, location, and employer.

What is the difference between Safety Surveillance Associate vs Clinical Data Coordinator?

AspectSafety Surveillance AssociateClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in life sciences or related field; certifications like RAC or CCRA are a plusBachelor's degree in health sciences, life sciences, or related field; often requires experience with clinical data management
Work EnvironmentPharmaceutical or biotech companies, clinical research organizations, monitoring safety dataClinical trial sites, CROs, or pharmaceutical companies managing data entry and validation
Employer & Industry UsageUsed in pharma, biotech, and clinical research to monitor safety reportsUsed in clinical research to manage and coordinate clinical trial data

The Safety Surveillance Associate focuses on monitoring and reporting safety data during clinical trials, ensuring compliance with safety regulations. In contrast, the Clinical Data Coordinator manages and validates clinical trial data to ensure accuracy. Both roles are essential in clinical research but serve different functions within the process.

What does a Safety Surveillance Associate do?

A Safety Surveillance Associate monitors and evaluates the safety of pharmaceutical or medical products by reviewing adverse event reports, clinical data, and safety signals. They ensure compliance with regulatory requirements and may use safety databases and tools to identify potential risks, supporting ongoing product safety assessments. Strong attention to detail and knowledge of pharmacovigilance practices are essential for this role.

What is a safety surveillance associate?

A safety surveillance associate is responsible for monitoring and assessing the safety of pharmaceutical or medical products during clinical trials or post-market. They review safety data, report adverse events, and ensure compliance with regulatory requirements, often using specialized databases and tools. Strong attention to detail and knowledge of pharmacovigilance are essential for this role.

What cities are hiring for Safety Surveillance Associate jobs?

Cities with the most Safety Surveillance Associate job openings:

What states have the most Safety Surveillance Associate jobs?

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Safety Surveillance Associate jobs near you
Infographic showing various Safety Surveillance Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, 1% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $54,467 per year, or $26.2 per hour.

Head of Multiple Myeloma & AML, Oncology - Global Patient Safety

Irvine, CA • On-site

Allergan
See more jobs at Allerganexternal

Other

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Job description

Company Description

About AbbVie

AbbVie'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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors, and Executive Medical Directors. Leading Product Safety Teams (PST) and support one or more products as the PST Lead and ensuring safety of one or more products through the product lifecycle (e.g. surveillance, signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities.

Responsibilities
  • Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance
  • Responsible for safety surveillance for pharmaceutical / biological / drug –device combined products
  • Lead and set the strategy for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans
  • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents
  • Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross-functional teams
  • Effectively write, review and provide input on technical documents independently
    Oversight and responsibility for leading the strategy for periodic reports (PSUR’s, PADER’s etc.)
  • Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials and post marketing
  • Responsible for implementing risk management strategies for assigned products
  • Proactively engaging, inspiring, coaching and mentoring team and colleagues
  • Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors: performance and talent management, coaching and development.
  • Assumes responsibility for coordinating and overseeing safety related activities at a product level across multiple indications or multiple related products for the same indication. Is responsible for assessing product safety strategy across the entire program and for overseeing approval related activities.
Qualifications
  • MD / DO with 2+ years of residency with patient management experience
    Master Public Health is preferred in addition to MD / DO, not required
    8 - 10 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry
  • Effectively analyze and guide analysis of clinical data and epidemiological information
  • Effectively present recommendations / opinions in group environment both internally and externally
  • Write, review and provide input on technical documents
    Work collaboratively and lead cross-functional teams
  • Ability to lead cross-functional teams in a collaborative environment
    Fluency, both written and oral, in English
  • Evaluate and make independent decisions. Ability to work effectively in the situation of uncertainty and complexity, ability to multitask
Additional Information

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie 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

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