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Manager Adverse Event Reporting Jobs (NOW HIRING)

millenniumsoft

Clinical Risk Specialist I

Covington, GA · On-site

The Clinical Risk Specialist I will perform MDR/adverse event reporting, evaluate clinical use of ... Assess clinical risk of reported complaints using risk management tools (DFMEA), medical literature ...

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How much do manager adverse event reporting jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for manager adverse event reporting in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.

What are Manager Adverse Event Reporting jobs?

Manager Adverse Event Reporting jobs involve overseeing the process of identifying, documenting, and reporting adverse events related to pharmaceutical products, medical devices, or clinical trials. These managers ensure compliance with regulatory requirements, coordinate with cross-functional teams, and implement procedures to accurately capture and report safety data. They play a critical role in maintaining patient safety and regulatory compliance, often interacting with regulatory agencies and internal stakeholders. Strong knowledge of pharmacovigilance, regulatory guidelines, and project management is essential for this role.

What are the key skills and qualifications needed to thrive as a Manager Adverse Event Reporting, and why are they important?

To thrive as a Manager Adverse Event Reporting, you need a strong background in pharmacovigilance, regulatory compliance, and life sciences, often supported by a relevant bachelor’s or advanced degree. Familiarity with safety databases, MedDRA coding, and global regulatory reporting systems such as EudraVigilance and FDA safety reporting tools is essential. Strong attention to detail, leadership, and excellent communication skills help ensure accurate reporting and effective team management. These competencies are crucial for maintaining patient safety, regulatory compliance, and the integrity of pharmacovigilance operations.

What are some of the main challenges faced by a Manager Adverse Event Reporting, and how can they be addressed?

A Manager Adverse Event Reporting often faces challenges such as ensuring timely and accurate reporting of adverse events to regulatory authorities, managing large volumes of data, and staying updated with evolving regulatory requirements. Effective communication and collaboration with cross-functional teams like clinical, regulatory, and safety are essential to maintain compliance and data integrity. Utilizing robust pharmacovigilance systems and fostering ongoing training for team members can significantly mitigate these challenges and ensure smooth operations.
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What cities are hiring for Manager Adverse Event Reporting jobs? Cities with the most Manager Adverse Event Reporting job openings:
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Manager Adverse Event Reporting jobs near you
Infographic showing various Manager Adverse Event Reporting job openings in the United States as of May 2026, with employment types broken down into 90% Full Time, 7% Part Time, 1% Temporary, and 2% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.
Clinical Trial & Pharmacovigilance Manager

Clinical Trial & Pharmacovigilance Manager

Venesco LLC

Falls Church, VA • On-site

Full-time

Posted 2 days ago

Job description

Clinical Trial & Pharmacovigilance Manager
Location: Hybrid
Job Type: Full-Time
About the Role
We are seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical studies and ensure robust safety surveillance.
Requirements
Key Responsibilities
  • Manage clinical trial operations from startup to closeout
  • Oversee adverse event reporting and pharmacovigilance systems
  • Ensure compliance with GCP and regulatory requirements
  • Coordinate DSMB activities and safety reviews
  • Develop and manage clinical study documentation
  • Collaborate with regulatory teams on submissions

Qualifications
  • Advanced degree in clinical research, life sciences, or healthcare field
  • 8+ years of clinical operations and safety experience
  • Strong knowledge of ICH-GCP and FDA regulations

Preferred
  • Experience with safety databases (Argus, ArisG)
  • Clinical trial management certification

Apply