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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 Remote 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: Boston, Massachusetts (Home-Based)
Job Type: Full-time


ABOUT MEDPACE

Medpace is an innovative, scientifically oriented global contract research organization (CRO). We specialize in full-service project work and aim to accelerate the global development of safe and effective medical therapeutics.

Medpace provides specialized services to the biotechnology, pharmaceutical, and medical device industries across multiple therapeutic areas, including hematology/oncology.


JOB SUMMARY

Medpace is seeking experienced Clinical Research Associates (CRAs) to join our Hematology/Oncology team. This home-based role offers the opportunity to be involved in groundbreaking clinical research while enjoying excellent compensation and benefits, including equity/stock options and additional bonus programs.

Medpace offers a Certificate Program in Hematology/Oncology Monitoring, providing specialized training in various cancer indications and treatment methods. We also offer certificate programs in other therapeutic areas like medical devices, rare diseases, infectious diseases, and COVID-19.


KEY RESPONSIBILITIES

Site Management & Monitoring

  • Conduct monitoring visits including qualification, initiation, monitoring, and closeout visits at research sites.
  • Ensure adherence to the protocol, ICH GCP guidelines, and applicable regulations.
  • Verify the eligibility of subjects for enrollment, ensuring that they meet study inclusion criteria.

Regulatory & Compliance

  • Review regulatory documents to ensure compliance.
  • Verify medical records and source documentation to ensure data accuracy and consistency.
  • Identify and report protocol deviations while maintaining proper documentation practices.

Patient Safety & Data Integrity

  • Verify adverse event (AE) and serious adverse event (SAE) reporting in accordance with the protocol.
  • Conduct medical device/investigational product accountability, ensuring proper handling, inventory, and storage.
  • Evaluate patient recruitment and retention metrics, offering suggestions for improvement where necessary.

Collaboration & Reporting

  • Communicate regularly with site staff including coordinators and clinical research physicians to ensure smooth site operations.
  • Complete monitoring reports and follow-up letters, summarizing key findings, deficiencies, and corrective actions.

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 relevant industry experience such as a study coordinator or clinician).
  • Experience in Hematology/Oncology is preferred.

Therapeutic Experience (Preferred):

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

Skills & Knowledge:

  • Strong knowledge of clinical trial processes, medical terminology, and patient management.
  • Attention to detail and excellent time management skills.
  • Strong communication and interpersonal skills.
  • Ability to travel nationwide as required.

COMPENSATION & BENEFITS

Salary & Benefits:

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

Career Growth & Perks:

  • Certificate Program in Hematology/Oncology and other therapeutic training.
  • Structured career path with opportunities for professional growth.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness initiatives.
  • Discounts for local businesses.

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 to accelerate your hematology/oncology career and make a lasting impact on global health. Apply now!

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