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Experienced Clinical Research Associate

2-4 years
Not Disclosed
10 Dec. 17, 2024
Job Description
Job Type: Full Time 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: Clinical Research Associate (CRA)
Company: Medpace

Job Summary:
At Medpace, our Clinical Research Associates (CRAs) come from diverse medical and science-related backgrounds. The role is ideal for individuals looking to enter the world of clinical research, including nurses, dieticians, pharmacy technicians, sales representatives, biotech engineers, PhD/Pharm.D candidates, health and wellness coordinators, and research assistants. Our PACE® – MEDPACE CRA TRAINING PROGRAM provides comprehensive training to help you grow into a skilled CRA with Medpace. This program, unlike any other in the industry, prepares you for success with interactive discussions, hands-on exercises, and clinical research departmental rotations.

Responsibilities:
As a CRA, your primary responsibilities will include:

  • Conduct qualification, initiation, monitoring, and closeout visits for research sites according to the approved protocol.
  • Communicate with medical site staff including coordinators and clinical research physicians.
  • Verify investigator qualifications, training, resources, and site conditions.
  • Review and verify medical records and research source documentation, ensuring accurate data reporting in compliance with the protocol.
  • Ensure that investigators are enrolling eligible subjects and review regulatory documents.
  • Account for medical devices/investigational products and monitor adverse events and concomitant medications.
  • Assess patient recruitment and retention efforts, providing suggestions for improvements.
  • Prepare monitoring reports, documenting findings, deviations, and recommending corrective actions.

Qualifications:

  • Bachelor's degree with 2-4 years of experience as a Clinical Research Associate.
  • Willingness to travel approximately 60-80% nationally.
  • Familiarity with Microsoft® Office.
  • Strong communication and presentation skills are a plus.

Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. We are committed to accelerating the global development of safe and effective therapeutics through our disciplined scientific approach. Medpace’s expertise spans oncology, cardiology, metabolic diseases, endocrinology, CNS, anti-viral, and anti-infective areas, with over 5,000 employees across more than 40 countries.

Why Medpace?

  • People. Purpose. Passion. Make a difference tomorrow by joining us today.
  • Our work over the past 30+ years has positively impacted patients and families across key therapeutic areas, and we continue to improve lives worldwide.

Medpace Perks:

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with professional growth opportunities
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Awards:

  • Recognized by Forbes as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
  • Awarded CRO Leadership Awards by Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility.