Experienced Clinical Research Associate - Hematology/Oncology

Medpace; Salt Lake City (UT); Remote; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking an Experienced Clinical Research Associate to join their dynamic team in the hematology and oncology field. This role offers the flexibility of home-based work while providing an opportunity to advance your career in clinical research. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and contributing to the advancement of medical therapeutics. With a strong focus on professional development, the company offers a Certificate Program in Hematology/Oncology Monitoring, making this an exciting opportunity for those passionate about making a difference in patient care.

Benefits

Equity/Stock Options

Additional Bonuses

Home-Based Role

Professional Development Programs

Qualifications

• 1+ years of clinical research experience required.
• Experience as a CRA, study coordinator, or clinician preferred.

Responsibilities

• Monitor clinical trials for hematology and oncology.
• Ensure compliance with regulatory standards and protocols.

Skills

Clinical Research Monitoring

Attention to Detail

Time Management

Communication Skills

Education

Bachelor's Degree in Health or Science

Job description

Experienced Clinical Research Associate - Hematology/Oncology

Join Medpace as an Experienced Clinical Research Associate and accelerate your career in hematology and oncology. We offer home-based roles with excellent compensation and benefits, including an equity/stock option program and additional bonuses.

Medpace is a scientifically oriented, mid-sized global CRO dedicated to advancing medical therapeutics. We provide a Certificate Program in Hematology/Oncology Monitoring, covering cancer overview, indications, treatments, and diagnostic criteria. Additional programs in medical device, rare disease, infectious disease, ATMP, and COVID-19 are also available.

Applicants with experience in monitoring as a CRA, study coordinator, or clinician in the following indications will be considered:

• Solid Tumors: Breast, Ovarian, Prostate, Colorectal, Bladder, Lung, Kidney, Pancreatic Cancer
• Small Cell Lung Cancer
• Graft vs Host Disease
• Glioblastoma
• Melanoma
• Leukemia
• Lymphoma
• Mesothelioma

Requirements include a Bachelor's degree in a health or science-related field, at least one year of clinical research or industry experience, ability to travel nationwide, and strong attention to detail, time management, and communication skills.