Experienced Clinical Research Associate - Hematology/Oncology

Job Summary A ccelerate your hematology/oncology career by joining Medpace! This is a home-based role with excellent compensation and benefits, including an Equity/Stock option program, and additional bonus opportunities. Medpace is growing quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work. Through our expedited PACE® Training Program, you will receive customized training and efficient onboarding to familiarize yourself with Medpace systems. We also offer a certificate program (advanced training curricula) in hematology/oncology monitoring, which includes a general cancer overview, common indications, treatment options, diagnostic and reference criteria. If you're interested in expanding your therapeutic area expertise, Medpace also offers certificate programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP), and COVID-19. We are seeking applicants with experience in the following indications: Solid Tumor Breast, Ovarian, Prostate, Colorectal, Bladder, Lung, Kidney, Pancreatic Cancer Small Cell Lung Cancer Graft vs Host Disease Glioblastoma Melanoma Leukemia Lymphoma Mesothelioma We Offer the Following: Competitive travel bonus Equity/Stock option program Training completion and retention bonus Annual merit increases 401K matching Opportunity to work from home Flexible work hours across days within a week Retain airline reward miles and hotel reward points Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere In-house travel agents, reimbursement for airline club membership, and TSA pre-check Opportunity for leadership positions – Lead CRA, CRA Manager, Training and Development Manager, and many more User friendly CTMS with electronic submission and approval of monitoring visit reports; Customized, expedited PACE® training program based on your experience, therapeutic background, and interest Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts In-house administrative support for all levels of CRA Opportunity to work with international team of CRAs Responsibilities Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol Communication with the medical site staff including coordinators, clinical research physicians, and their site staff Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward Verification the investigator is enrolling only eligible subjects Regulatory document review Medical device and/or investigational product/drug accountability and inventory Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance Qualifications Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred Ability to travel 60-70% to locations nationwide is required Minimum of a bachelor’s degree in a health or science related field Proficient knowledge of Microsoft Office Strong communication and presentation skills Detail-oriented and efficient in time management #LI-Remote Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive PTO packages – starting at 20+ days Company-sponsored employee appreciation events Employee health and wellness initiatives Competitive compensation and benefits package Structured career paths with opportunities for professional growth Discounts for local businesses Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.