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Experienced Clinical Research Associate - Hematology/Oncology

1-3 years
Not Disclosed
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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