Experienced Clinical Research Associate - Hematology/Oncology

Medpace

1-3 years

Not Disclosed

Cincinnati OH

10 Feb. 12, 2025

Job Description

Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Experienced Clinical Research Associate - Hematology/Oncology

Location: Cincinnati, Ohio (Home-Based with Hybrid Optional)
Job Type: Full-time

ABOUT MEDPACE

Medpace is an innovative, scientifically oriented global contract research organization (CRO) that is focused on full-service project work. Our mission is to accelerate the global development of safe and effective medical therapeutics. We work across various therapeutic areas, including hematology/oncology, to positively impact patients' lives worldwide.

JOB SUMMARY

Medpace is seeking experienced Clinical Research Associates (CRAs) to join our Hematology/Oncology team. This home-based role offers competitive compensation, including equity/stock options and bonus programs. The position also provides the opportunity for career advancement and access to specialized training programs such as the Certificate Program in Hematology/Oncology Monitoring.

Candidates with experience in a range of oncology indications are encouraged to apply. These include experience as a CRA, study coordinator, or clinician in relevant therapeutic areas.

KEY RESPONSIBILITIES

Site Management & Monitoring

Conduct monitoring visits (qualification, initiation, monitoring, and closeout) at research sites in compliance with the protocol.
Communicate effectively with site staff, including coordinators, clinical research physicians, and investigators.
Verify eligibility of study participants to ensure they meet the inclusion criteria.
Ensure adherence to good clinical practice (GCP) and other applicable regulatory requirements.

Regulatory & Compliance

Review and verify regulatory documents to ensure full compliance with applicable regulations and standards.
Verify medical records and source documentation against case report form data, ensuring accuracy and consistency.
Report protocol deviations and ensure proper documentation practices are followed.

Patient Safety & Data Integrity

Monitor adverse events (AEs) and serious adverse events (SAEs), ensuring accurate reporting in accordance with the protocol.
Verify medical device and investigational product accountability and inventory.
Assess and improve patient recruitment and retention efforts at clinical sites.

Reporting & Communication

Complete monitoring reports and follow-up letters, summarizing key findings and corrective actions.
Ensure site adherence to the study protocol and provide recommendations for improvements.

QUALIFICATIONS & EXPERIENCE

Education:

Bachelor’s degree in a health or science-related field.

Experience:

At least one year of clinical research experience as a CRA or in a relevant role (e.g., study coordinator or clinician).
Prior experience in hematology/oncology is preferred.

Therapeutic Experience (Preferred):

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

Skills & Competencies:

Strong communication and time management skills.
Attention to detail and ability to maintain high levels of accuracy in data management.
Nationwide travel availability as required by the position.

COMPENSATION & BENEFITS

Salary & Benefits:

Competitive salary based on experience.
Equity/Stock Option Program and bonus programs.
Comprehensive benefits package: Health, dental, and vision insurance.
Flexible work environment (home-based role with hybrid options).
Generous PTO package, starting at 20+ days.

Career Growth & Perks:

Certificate Program in Hematology/Oncology Monitoring and other specialized therapeutic training.
Structured career paths with opportunities for professional growth.
Employee wellness initiatives and company-sponsored appreciation events.
Discounts for local sports games, fitness gyms, and attractions.
Discounted tuition for online programs at the University of Cincinnati.

AWARDS & RECOGNITION

Top Workplace in 2024 by The Cincinnati Enquirer.
Forbes: Recognized as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

HOW TO APPLY

Join Medpace today and accelerate your hematology/oncology career while making a lasting impact on global health. Apply now to be part of our rapidly growing team!

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