Clinical Monitoring Intern (Summer 2025) - Dallas

0-2 years
Not Disclosed
10 March 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Monitoring Intern (Summer 2025) - Dallas

Location: Irving (Dallas), Texas
Department: Clinical Research Associate
Job ID: 11190

Job Summary:
Our clinical operations activities are growing rapidly, and we are currently seeking full-time, Dallas office-based Clinical Monitoring Interns to join our team this summer! This internship will provide insight into the day-to-day responsibilities of a Clinical Research Associate. You will receive hands-on training and support various projects within Clinical Operations.

Responsibilities:

  • Become familiar with ICH-GCP guidelines, industry regulations, and Medpace systems;
  • Support the Clinical Monitoring team in conducting clinical site activities;
  • Explore and shadow other opportunities for new grads within Clinical Research;
  • Provide day-to-day departmental and project support;
  • Observe CRA PACE® training sessions;
  • Conduct quality control of documents;
  • Assist with CRA recruitment initiatives;
  • Maintain spreadsheets and compile reports;
  • Perform other tasks as needed.

Qualifications:

  • Working towards a Bachelor’s degree in a Life Science-related field, with expected graduation in Fall 2025 or Spring 2026;
  • Local to Dallas, TX, or the surrounding area;
  • Excellent organizational, communication, and prioritization skills;
  • Knowledge of Microsoft Office.

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 a 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, we employ more than 5,000 people across 40+ countries.

Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join 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.

Dallas Perks:

  • Flexible work environment;
  • Competitive PTO packages, starting at 20+ days;
  • Competitive compensation and benefits package;
  • Company-sponsored employee appreciation events;
  • Employee health and wellness initiatives;
  • Community involvement with nonprofit organizations;
  • Structured career paths with opportunities for professional growth;
  • Discounts on local sports games, fitness gyms, and attractions;
  • Modern, eco-friendly campus with an on-site fitness center;
  • Free on-site parking;
  • Outdoor seating and workspace.

Awards:

  • Recognized by Forbes as one of America's Best Midsize Companies in 2021, 2022, and 2023;
  • 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 the next steps.

EO/AA Employer: M/F/Disability/Vets