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Drug Safety Associate (Life Sciences Degrees)

0-2 years
Not Disclosed
10 Oct. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Drug Safety Associate (Life Sciences Degrees)

📍 Location: Cincinnati, Ohio
🏢 Department: Clinical Safety
🆔 Job ID: 11670
💼 Organization: Medpace


🔹 Job Summary

Medpace is seeking a detail-oriented and motivated Drug Safety Associate (Clinical Safety Coordinator) to join our Clinical Safety Department on a full-time, office-based basis in Cincinnati, Ohio.

This role focuses on the collection, processing, and tracking of adverse events from multiple sources — including clinical trials and post-marketing surveillance. It’s an exciting opportunity to apply your life sciences background while building a career in Pharmacovigilance (PV) and Clinical Safety within a global CRO environment.

🚀 If you’re passionate about patient safety, data accuracy, and clinical excellence, this role is your first step toward a rewarding PV career.


🔹 Key Responsibilities

  • Collect, process, and track Serious Adverse Event (SAE) reports from various sources.

  • Prepare and review safety narratives and generate relevant queries.

  • Perform data entry and case management within the safety database.

  • Conduct quality control (QC) checks on safety cases for completeness and accuracy.

  • Collaborate with cross-functional teams and clinical research sites to ensure compliance with Medpace SOPs and regulatory safety requirements.


🔹 Qualifications

  • Education: Bachelor’s degree in Life or Health Sciences (e.g., Microbiology, Biology, Pharmaceutical Sciences, Chemistry, or related disciplines).

  • Skills Required:

    • Strong command of medical terminology.

    • Proficient in Microsoft Office (Word, Excel, Outlook).

    • Excellent organizational and communication skills.

    • Keen attention to detail and accuracy in documentation.


🔹 About Medpace

Medpace is a global, full-service Clinical Research Organization (CRO) specializing in Phase I–IV clinical development services for the biotechnology, pharmaceutical, and medical device industries.

Our mission is to accelerate the global development of safe and effective medical therapeutics through scientific expertise and operational excellence.

Headquarters: Cincinnati, Ohio
Global Presence: 40+ countries | Employees: 5,000+


🔹 Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

For over 30 years, Medpace has improved the lives of patients and families worldwide through innovative clinical research across major therapeutic areas.


🔹 Cincinnati Campus Perks

  • Flexible and collaborative work environment

  • 20+ days starting PTO with competitive salary and benefits

  • Modern eco-friendly campus with an on-site fitness center

  • Employee health and wellness programs

  • Company-sponsored appreciation events

  • Active community involvement with local non-profit organizations

  • Discounts on local sports, gyms, and entertainment venues

  • Structured career development and promotion pathways

  • Tuition discounts for University of Cincinnati online programs


🔹 Awards & Recognition

🏆 Top Workplace 2024The Cincinnati Enquirer
🏆 Forbes: America’s Most Successful Midsize Companies (2021–2024)
🏆 CRO Leadership AwardsLife Science Leader Magazine
(Recognized for expertise, quality, capabilities, reliability, and compatibility)


🔹 What to Expect Next

After reviewing your application, a Medpace recruitment representative will contact you with details regarding the next steps if your qualifications align with this position.


🖱️ Apply Now

Join Medpace’s Clinical Safety team and play a key role in ensuring patient safety across global clinical trials.
Apply today or share this opportunity with your network!