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Experienced Clinical Research Associate - Hematology/Oncology

Medpace
1+ years
USD $90,000–$140,000
Cincinnati, United States
15 June 24, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Experienced Clinical Research Associate – Hematology/Oncology

Company: Medpace
Job Title: Experienced Clinical Research Associate – Hematology/Oncology
Job ID: 11851
Location: Cincinnati, Ohio, USA (Home-Based Opportunity Available)

Salary: USD $90,000–$140,000 per year (Estimated based on CRA experience, oncology expertise, and location) + Equity/Stock Options + Performance Bonuses + Benefits


Job Summary

Medpace is seeking experienced Clinical Research Associates (CRAs) to join its Hematology/Oncology team. This role offers the opportunity to work on cutting-edge oncology clinical trials while advancing therapeutic expertise through Medpace's specialized Hematology/Oncology Certificate Program.

The position is home-based and includes excellent compensation, stock option eligibility, bonus programs, and comprehensive benefits.


Hematology/Oncology Certificate Program

Medpace provides advanced training through its specialized Oncology Monitoring Certificate Program, covering:

  • General cancer overview

  • Common oncology indications

  • Treatment options and standards of care

  • Diagnostic criteria

  • Response evaluation and reference criteria

Additional Certificate Programs are available in:

  • Medical Devices

  • Rare Diseases

  • Infectious Diseases

  • Advanced Therapy Medicinal Products (ATMP)

  • COVID-19 Research


Therapeutic Areas & Disease Experience

Candidates with experience in any of the following indications are encouraged to apply:

Solid Tumors

  • Breast Cancer

  • Ovarian Cancer

  • Prostate Cancer

  • Colorectal Cancer

  • Bladder Cancer

  • Lung Cancer

  • Kidney Cancer

  • Pancreatic Cancer

Hematology & Oncology Indications

  • Small Cell Lung Cancer

  • Graft-versus-Host Disease (GvHD)

  • Glioblastoma

  • Melanoma

  • Leukemia

  • Lymphoma

  • Mesothelioma

Relevant experience may include clinical monitoring as a CRA, Clinical Research Coordinator (CRC), or clinical practice experience.


Key Responsibilities

  • Monitor oncology and hematology clinical trials

  • Conduct site qualification, initiation, monitoring, and closeout visits

  • Ensure protocol, GCP, and regulatory compliance

  • Review source documents and clinical trial data

  • Verify patient eligibility and enrollment criteria

  • Assess investigational product accountability

  • Review adverse events and safety reporting

  • Support site performance and patient recruitment activities

  • Prepare monitoring reports and follow-up documentation

  • Collaborate with investigators, coordinators, and study teams


Eligibility Criteria

Required Qualifications

  • Bachelor's degree in Life Sciences, Health Sciences, Pharmacy, Nursing, Biotechnology, or a related scientific field

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

  • Experience in oncology or hematology studies preferred

  • Ability to travel nationwide

  • Strong attention to detail

  • Excellent time management skills

  • Effective communication and interpersonal abilities


Compensation & Benefits

  • Competitive salary package

  • Equity/Stock Option Program

  • Additional performance-based bonus programs

  • Comprehensive health and wellness benefits

  • Flexible home-based work environment

  • Career development and certification opportunities

  • Structured promotion and leadership pathways


Employee Perks

  • 20+ days Paid Time Off (PTO)

  • Employee appreciation events

  • Community involvement initiatives

  • Discounts on sports events, fitness centers, and attractions

  • Modern eco-friendly campus facilities

  • On-site fitness center

  • Discounted tuition programs through local educational partnerships


About Medpace

Medpace is a leading global Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, Ohio, Medpace employs over 6,000 professionals across more than 40 countries and supports clinical research in oncology, cardiology, endocrinology, metabolic disorders, CNS diseases, infectious diseases, and other therapeutic areas.


Awards & Recognition

  • Top Workplace 2024 – Cincinnati Enquirer

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

  • Multiple CRO Leadership Awards recognizing quality, expertise, reliability, and innovation