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Intern, Reimbursement, Healthcare Economics & Market Access (RHEMA)

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MCRA

1mo ago

  • Internship
    Full-time
    Summer Internship
  • Government & Politics
    Research & Development
  • Washington
  • Quick Apply

AI generated summary

  • You must be an incoming junior pursuing Economics, Public Policy, Healthcare, or Business, with strong research skills.
  • You will analyze prior reimbursement landscapes, assess client positions in the reimbursement lifecycle, and research a topic for a significant project presentation.

Requirements

  • Currently pursuing Economics, Public Policy, Healthcare, or Business.
  • Incoming Junior.
  • Strong research skills.

Responsibilities

  • Review prior reimbursement landscape analyses to determine next steps, followed by an analysis of where those clients likely sit in the reimbursement lifecycle to identify candidates for future outreach.
  • Interns will research a specific topic and complete a meaningful project presentation.

FAQs

What is the duration of the internship program?

The internship program lasts for 8 weeks, from June 2, 2025, to July 25, 2025.

What are the working hours for the internship?

Interns are expected to work 25 hours per week, approximately 5 hours per day from 9:00 AM to 3:00 PM, although specific schedules may vary.

What qualifications are required to apply for this internship?

Applicants should be currently pursuing a degree in Economics, Public Policy, Healthcare, or Business and must be incoming juniors.

Will interns receive any equipment for the internship?

Yes, interns will be provided with a laptop and other required equipment.

What type of projects will interns work on during the program?

Interns will conduct research on a specific topic and complete a meaningful project presentation, which may include analyzing reimbursement landscapes and identifying candidates for future outreach.

Where is the internship located?

The internship is based in Washington, DC, and follows a hybrid schedule.

What type of firm is MCRA?

MCRA is a leading medical device advisory firm and clinical research organization (CRO) that focuses on regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance.

Is there an opportunity for professional development during the internship?

Yes, interns will work closely with MCRA experts and mentors to gain hands-on knowledge and valuable experience in RHEMA.

Does MCRA have a commitment to diversity and inclusion?

Yes, MCRA is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants receive consideration for employment without regard to legally protected characteristics.

Leading Global Full-Service Medical Device, Diagnostics & Biologics CRO & Integrated Consulting Advisory Firm.

Manufacturing & Electronics
Industry
51-200
Employees
2004
Founded Year

Mission & Purpose

MCRA is the leading global full-service medical device, diagnostics, and biologics CRO and consulting advisory firm. MCRA delivers to its client’s industry experience, integrating its seven business value creators: regulatory, clinical research, reimbursement, healthcare compliance, quality assurance, due diligence and distribution logistics to provide a dynamic, market-leading effort from innovation conception to commercialization. MCRA’s integrated application of these key value-creating initiatives provides unparalleled value for its clients. MCRA has offices in Washington, DC, Hartford, CT, New York, NY, London, England, Winterthur, Switzerland, Eschborn, Germany and Tokyo, Japan and serves nearly 1,000 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, biologics, cardiovascular, diagnostic imaging, wound care, artificial intelligence, dental, anesthesia, general surgery, digital health, neurology, robotics, oncology, general and plastic surgery, urology, and in vitro diagnostic (IVD) devices and medical device cybersecurity. MCRA places particular emphasis on its expertise working with companies in all stages of development and throughout the technology life cycle by ushering technologies from the conceptual pre-clinical stage to market approval.