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Experienced Clinical Research Associate - Hematology/Oncology

1+ years
Not Disclosed
10 Nov. 21, 2025
Job Description
Job Type: Full Time Remote 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

Experienced Clinical Research Associate – Hematology/Oncology

Location: Cincinnati, Ohio (Home-Based / Remote Options Available)
Job Category: Clinical Research Associate
Job ID: 10812


Job Summary

Medpace, a globally recognized mid-sized Clinical Research Organization (CRO), is seeking experienced Clinical Research Associates (CRA) specializing in Hematology and Oncology. This role provides a home-based working option with competitive compensation, including equity/stock options and bonus programs.

This is an exceptional opportunity to advance your clinical research career while contributing to the global development of safe and effective therapeutics across key oncology indications.


Key Responsibilities

  • Monitor and oversee clinical trials in Hematology and Oncology, ensuring compliance with ICH/GCP guidelines.

  • Conduct site visits, verify study conduct, patient safety, and data integrity.

  • Prepare and maintain accurate study documentation, ensuring regulatory compliance.

  • Participate in Medpace’s Certificate Programs, including advanced Hematology/Oncology monitoring and other therapeutic areas such as medical devices, rare diseases, infectious diseases, ATMPs, and COVID-19 studies.

  • Collaborate with clinical teams, study coordinators, and site staff to optimize trial efficiency and data quality.


Targeted Therapeutic Areas

  • Solid Tumors: Breast, Ovarian, Prostate, Colorectal, Bladder, Lung, Kidney, Pancreatic

  • Small Cell Lung Cancer

  • Graft vs Host Disease

  • Glioblastoma

  • Melanoma

  • Leukemia and Lymphoma

  • Mesothelioma


Experience & Qualifications Required

  • Bachelor’s degree in a health or science-related field (advanced degree preferred).

  • Minimum 1 year of clinical research experience or equivalent direct industry experience (e.g., Clinical Research Coordinator).

  • Proven experience in CRA roles, study coordination, or clinical monitoring is highly desirable.

  • Ability to travel nationally as required.

  • Strong attention to detail, time management, and communication skills.


Why Join Medpace?

  • Work with a globally recognized CRO that has positively impacted patient care across multiple therapeutic areas for over 30 years.

  • Access structured career advancement, advanced training, and leadership development programs.

  • Flexible home-based roles for qualified candidates.

  • Be part of a team that directly contributes to advancing medical therapeutics worldwide.


Cincinnati Campus & Benefits

  • Flexible work arrangements with remote options.

  • PTO starting at 20+ days annually.

  • Competitive compensation, equity programs, and benefits.

  • Employee wellness initiatives and recognition events.

  • Modern, eco-friendly campus with on-site fitness facilities.

  • Community engagement opportunities and local discounts.

  • Tuition discounts for University of Cincinnati online programs.


Awards & Recognition

  • Top Workplace 2024 – The Cincinnati Enquirer

  • Forbes America’s Most Successful Midsize Companies (2021–2024)

  • CRO Leadership Awards – Life Science Leader magazine for quality, expertise, and reliability


Next Steps

Qualified candidates will be reviewed by Medpace’s recruitment team. Shortlisted applicants will be contacted for the next steps in the hiring process.