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Join a forward-thinking company as an Experienced Clinical Research Associate specializing in Hematology/Oncology. This role offers the flexibility of home-based work while contributing to the development of safe medical therapeutics. You'll be part of a dedicated team, ensuring the highest standards in clinical trials. With excellent compensation and benefits, including equity options and bonuses, this opportunity is perfect for those passionate about making a difference in patient lives. Embrace a career that values your skills and offers growth in a supportive environment.
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Join Medpace as an Experienced Clinical Research Associate specializing in Hematology/Oncology!
Enjoy home-based roles with excellent compensation, benefits, and additional programs such as equity/stock options and bonuses.
Medpace is a mid-sized, global CRO focused on full-service project work, dedicated to accelerating the development of safe and effective medical therapeutics. We offer advanced training in Hematology/Oncology Monitoring and other therapeutic areas.
Applicants with experience in monitoring, study coordination, or clinical roles in indications such as Solid Tumors, Small Cell Lung Cancer, Graft vs Host Disease, Glioblastoma, Melanoma, Leukemia, Lymphoma, or Mesothelioma are encouraged to apply. A minimum of a Bachelor's degree in a health or science field and at least one year of relevant experience are required. Candidates must be able to travel nationwide and possess strong attention to detail, time management, and communication skills.
We are committed to making a difference and have a rich history of positively impacting patient lives. Benefits include a flexible work environment, competitive PTO, health and wellness initiatives, community involvement, and career growth opportunities. Recognized as a top workplace and one of America's most successful midsize companies, we value our employees and their contributions.
Next steps involve a review of your qualifications by a Medpace team member, with potential contact for further discussion.