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Clinical Safety Reviewer Jobs (NOW HIRING)

MSD Malaysia

$378 - $595/hr

Serve as Physician Management Reviewer for post-approval safety signal evaluations.* Establish and ... Partner with Clinical Development, Regulatory Affairs, Biostatistics, Epidemiology, and other ...

MicroVention

Specialist, Clinical Safety (US Remote)

$105K - $131K/yr

Draft, review, and provide input to the clinical safety components of clinical study protocols, study reports, safety manuals, safety CRFs, study supporting materials, and other related documentation.

UCB

Non-Clinical Safety Lead - Cambridge, MA

Cambridge, MA · On-site

$168K - $220K/yr

Oversee the design, review, and interpretation of non-clinical studies. * Manage non-clinical safety programs, including budgets. Interested? For this role you'll need the following education ...

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Clinical Safety Reviewer information

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How much do clinical safety reviewer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical safety reviewer in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $31.25 and $40.38 per hour, depending on experience, location, and employer.

What is a clinical safety reviewer?

Clinical Safety Reviewers are professionals responsible for evaluating and monitoring the safety of pharmaceutical products and medical devices during clinical trials. They review clinical data to identify potential safety concerns, assess adverse event reports, and ensure that all regulatory requirements regarding patient safety are met. Clinical Safety Reviewers collaborate with medical teams, regulatory agencies, and other stakeholders to ensure the safety and well-being of trial participants. Their work is crucial in minimizing risks and ensuring that treatments are safe before they reach the market.

How does a clinical safety reviewer typically collaborate with other teams during the drug development process?

Clinical Safety Reviewers work closely with cross-functional teams such as clinical operations, data management, medical monitors, and regulatory affairs. They regularly communicate findings from safety data analyses, contribute to safety review meetings, and provide input for safety sections in regulatory submissions. This collaborative approach ensures that safety signals are identified early and managed appropriately, supporting both patient wellbeing and project timelines. Strong teamwork and clear communication are essential for success in this role.

What are the key skills and qualifications needed to thrive as a clinical safety reviewer, and why are they important?

To thrive as a Clinical Safety Reviewer, you need a strong background in life sciences or pharmacy, experience in pharmacovigilance, and knowledge of regulatory requirements such as ICH guidelines. Familiarity with safety databases (like Argus or ArisGlobal), MedDRA coding, and case processing systems is typically required. Attention to detail, critical thinking, and effective communication are standout soft skills in this role. These capabilities ensure accurate safety assessment, regulatory compliance, and the protection of patient well-being in clinical trials.

What is the difference between Clinical Safety Reviewer vs Pharmacovigilance Associate?

AspectClinical Safety ReviewerPharmacovigilance Associate
Required CredentialsBachelor's degree, life sciences background, possibly certification in drug safetyBachelor's degree, life sciences background, often entry-level
Work EnvironmentPharmaceutical companies, CROs, clinical trial settingsPharmaceutical companies, CROs, regulatory agencies
Employer & Industry UsageFocuses on safety data review during clinical trials and post-marketingSupports safety data processing, case entry, and reporting
Common Search & Comparison IntentUnderstanding safety review roles in clinical trialsEntry-level safety data support roles

The Clinical Safety Reviewer primarily evaluates safety data during clinical trials and post-marketing, requiring specialized safety knowledge. In contrast, the Pharmacovigilance Associate handles data entry, case processing, and supports safety reporting. Both roles are essential in drug safety but differ in responsibilities and experience levels.

More about Clinical Safety Reviewer jobs

What job categories do people searching Clinical Safety Reviewer jobs look for?

The top searched job categories for Clinical Safety Reviewer jobs are:

Clinical Safety Reviewer jobs near you
Infographic showing various Clinical Safety Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $74,707 per year, or $35.9 per hour.

Clinical Safety Specialist

4 C Medical Technologies

Maple Grove, MN

$88K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago

Job description

Description

WHO WE ARE: 

If you're energized by collaboration, driven by purpose, and ready to take ownership of your impact, 4C Medical offers more than just a job-we offer the opportunity to help shape the future of medical innovation. As a growing medical device startup, every team member plays a critical role in advancing technologies that improve patient lives.


At 4C Medical, you'll find an environment where your ideas matter, your growth is prioritized, and your contributions directly influence our success. We're committed to fostering both personal and professional development in a culture built on accountability, curiosity, and shared purpose.


THE OPPORTUNITY

We are looking for a motivated Clinical Safety Specialist who is a hands-on, responsible for the day-to-day execution of safety activities for our investigational heart valve. This position ensures adverse events are accurately processed, documented, and reported in compliance with regulatory requirements.  Working on-site alongside Clinical, Regulatory, and Data teams, this role plays a critical part in maintaining real-time visibility into patient safety and ensuring inspection readiness throughout the clinical trial.


HOW YOU WILL CONTIRBUTE

Adverse Event Case Processing

  • Review, assess, and process adverse events (AEs) and serious adverse events (SAEs) from clinical studies 
  • Thorough review source documents and identifying missing information
  • Ensure completeness and accuracy of clinical study data, Data entry into the clinical trial  database in a timely manner
  • Follow up with site managers and internal teams to resolve data gaps quickly 

Safety Reporting & Documentation

  • Prepare safety narratives and support submission of regulatory reports within required timelines 
  • Prepare documentation binders for safety meetings
  • Taking and distributing meeting minutes 
  • Preparing and distributing site follow up letters
  • Maintain accurate, organized, and inspection-ready safety documentation 
  • Track case status and reporting timelines to ensure compliance 

Compliance & Quality

  • Adhere to company SOPs, ICH-GCP guidelines, and FDA regulations 
  • Support internal audits and regulatory inspections 
  • Identify and escalate data quality issues or compliance risks in real time 

Onsite Collaboration & Communication

  • Partner closely with Clinical Operations, Data Management, and Regulatory teams in a highly collaborative, onsite environment 
  • Communicate proactively on  case status, issues, and timelines 
  • Support training of internal teams and clinical sites on safety reporting expectations 
  • Schedule safety meetings and maintain calendar and checklist of timelines

WHY JOIN US

We recognize that meaningful work is supported by meaningful benefits. That's why we offer a competitive compensation package along with comprehensive benefits designed to support you and your family's health, well-being, and financial future.Our benefits package includes:

  • Medical
  • Dental
  • Vision
  • Flexible Spending Account (FSA)
  • Basic Life 
  • 401(k) Retirement Plan
  • Paid Holidays
  • PTO
  • Maternity/Paternity paid leave

It is 4C Medical's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state or local laws.  

Requirements

WHAT YOU NEED TO SUCCEED (Minimum Qualifications)

  • Bachelor's degree in Nursing (RN), Life Sciences, Pharmacy, or related field 
  • 3-5 years of experience in clinical research, pharmacovigilance, or healthcare safety/quality 
  • Working knowledge of  ICH-GCP and clinical trial safety reporting requirements 
  • Experience with clinical trial databases (CatchTrial, Medidata, etc.)
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, etc)

WHAT WILL SET YOU APART (Competencies)

  • Execution-focused: You reliably move cases from intake to submission without dropping details 
  • Attention to detail: You catch inconsistencies before they become compliance issues 
  • Time management: You handle multiple cases and deadlines without losing control 
  • Clear communication: You escalate issues quickly and effectively 
  • Collaborative mindset: You work well in a highly interactive, onsite team environment 

Apply