Clinical Research Associate

Location: Turbigo

The Clinical Research Associate position at Medpace offers the unique opportunity to have an  exciting career  in the research of drug and medical device development while  making a difference  in the lives of those around them. For those with a  medical and/or health/life science background  who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market— this could be the right opportunity for you!

Backgrounds of Successful CRAs

Nursing

Dietetics

Pharmacist

Pharmaceutical/Device Sales Representative

Biomedical/Chemical Engineer

PhD/Post-Doc

Pharm.

D candidate

Health and Wellness Coordinators

Clinical Research Coordinators

Research Assistants

MEDPACE CRA TRAINING PROGRAM (PACE)

PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA

PACE will prepare you by developing your CRA skills through interactive discussions and hands‑on job‑related exercises and practicums

To supplement your in‑house and field‑based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process

WHY BECOME A CRA

Dynamic working environment, with varying responsibilities day‑to‑day

Expansive experience in multiple therapeutic areas

Work within a team of therapeutic and regulatory experts

Defined CRA promotion and growth ladder with potential for mentoring and management advancements

Competitive pay

Bonus for CRA with 1.5-5 years of monitoring experience

Responsibilities

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol

Communication with the medical site staff including coordinators, clinical research physicians, and their site staff

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff

Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements

Verification that the investigator is enrolling only eligible subjects

Regulatory document review

Medical device and/or investigational product/drug accountability and inventory

Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement

Completion of monitoring reports and follow‑up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications

Master degree in health‑related field

Willing to travel 60-80% nationally

Familiarity with Microsoft® Office

CRA certification completed as per DMC 15/11/2011

Fluent in English and Italian language

Strong communication and presentation skills a plus

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 its 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, employing more than 5,000 people across 40+ countries.

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

Medpace Perks

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024

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 next steps.

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