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Safety Surveillance Associate Jobs (NOW HIRING)

MSD Malaysia

$66K - $90K/yr

Direct and oversee Safety Physicians and Medical Associates responsible for safety surveillance, signal detection, benefit-risk assessment, and risk management activities.* Ensure robust ...

Info Way Solutions

Quality Investigator

Sturtevant, WI · On-site

The Product Surveillance Associate position provides clinical and safety assessments of post-marketing events. This position is an integral role in marketing compliance with global regulations. Work ...

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$14

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$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:

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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.

Associate Manager, Product Surveillance

Racine, WI • On-site

Merz North America
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Merz North Americaexternal

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Key responsibilities

  • Coordinate, manage, and review complaints related to product safety and quality.

  • Lead post-market surveillance activities, including data compilation, assessment, and reporting.

  • Manage the product surveillance team through hiring, training, performance appraisal, and development.

Job description

About Us

Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.

A Brief Overview

The Associate Manager, Product Surveillance is responsible for providing tactical and strategic leadership for the Product Surveillance Associates for both technical and safety related complaints.  Day-to-day activities include coordination, management and review of Complaints.   Perform and/or assist with tasks required to oversee the proper operation and monitoring of Complaints as it pertains to Good Documentation Practices and Local and Global Regulations.  Oversee and/or assist with tasks related to the activities associated with operation of Merz North America Inc. Quality System and as directed. 

Manage the product surveillance staff including interviewing, hiring, training, and developing employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

Product Surveillance Activities

  • Support team by acting as a stream lead for all aspects of the complaint process.
  • Coordinate with Global Product Safety to evaluate and investigate patient-related complaints. Document consistent and compliant safety and reporting assessments.
  • Lead post market initiatives including compiling and assessing data for PSUR and other reports.
  • Lead risk management activities including review and coordination of post market data.
  • Review, approve, and close complaints in accordance with applicable SOP(s).
  • Manage the training program by developing, coordinating, and delivering training.
  • Maintain and update departmental metrics and reporting. Conduct statistical analysis of complaint trends, make conclusions, and drive actions including implementation of product updates or changes based on Complaint data.
  • Serve as the point of escalation and Quality Business Partner for commercial and customer relationships related to the complaint handling process.
  • Develop solutions to a variety of complex problems and identify corrective actions.

Process Improvement Initiatives

  • Proactively identify and implement operational changes to improve efficiencies in all aspects of complaint handling.
  • Drive continuous improvement initiatives / projects in Product Surveillance as well as items that arise as a result of complaint data.
  • Support/Conduct investigations associated with product deviations, product non-conformances, CAPAs, scrap, and rework. Analyze the data for the reasons of Quality Improvement and reporting.
  • Originate, review, and approve internal operating procedures and specifications through the Document Change process.
  • Support/Lead the development, verification, and validation of product changes and the introduction of new products as it relates to post market surveillance.

Compliance Initiatives

  • Lead internal quality system audits. Support and participate in external quality system audits.
  • Evaluate complaints and determine if the submission of a Medical Device Report (MDR) or other Vigilance Report is required.
  • Submit MDRs and Vigilance Reports according to regulatory timelines.
  • Maintain awareness of changes to global regulatory requirements related to complaint handling and adverse event reporting.

Leadership Responsibilities

  • Articulate a clear and compelling vision aligned with the global cultural tenets and strategic objectives of the company.
  • Clearly define roles and responsibilities while holding members accountable for their performance.
  • Develop talent and skills of individual team members
  • Empower leaders and employees to make informed decisions, enabling autonomy while providing guidance and support.

Minimum Qualifications 

Bachelor's Degree

Work Experience:

Required: 2+ years: Quality experience in Medical Device, Pharmaceutical and/or equivalent regulated industry

Preferred:

  • Experience with post market surveillance and complaint handling. 
  • Supervisor or Lead Experience

Knowledge, Skills, Abilities - Technical & Functional

Required:

  • Familiar with ISO 13485 Quality System Standards, FDA Quality System Regulations, GMPs, and/or other international medical device regulations.
  • Strong technical and general problem-solving skills; experience with NCR/CAPA processes
  • Medical and/or scientific terminology
  • Professional phone etiquette with the ability to appropriately handle sensitive information.
  • Proficient in Microsoft Office Suite, Adobe, and Quality System Management Software.
  • Highly organized with strong attention to detail.
  • Highly effective communication skills including written and verbal.
  • Proven leadership skills with the ability to manage and direct teams and projects, ensuring successful outcomes and effective collaboration.
  • Ability to work with company staff and communicate effectively throughout the organization.
  • Strong time management skills with proven ability to prioritize and manage multiple records/reports simultaneously.

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