Clinical Research Associate

Medpace; Monza; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

As a Clinical Research Associate at a leading clinical research organization, you will play a crucial role in the development of innovative drugs and medical devices. This position involves conducting site visits, ensuring compliance, and collaborating with medical teams. With comprehensive training provided, you will be equipped to enhance your skills and contribute significantly to the research and development field.

Servizi

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Competenze

• Master's degree in a health-related field is required.
• Willingness to travel 60-80% nationally.
• Strong communication and presentation skills are a plus.

Mansioni

• Conduct qualification, initiation, monitoring, and closeout visits at research sites.
• Communicate with medical site staff and verify adequate investigator qualifications.
• Complete monitoring reports and follow-up letters summarizing findings.

Conoscenze

Communication

Presentation

Formazione

Master's degree in a health-related field

Strumenti

Microsoft Office

Descrizione del lavoro

Job Summary

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!

Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include :

• 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)

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence :

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.

Responsibilities

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

Communicate 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.

Verify medical record and research source documentation against case report form data, including informing the site staff of any entry errors and ensuring good documentation practices are adhered to.

Verify that the investigator is enrolling only eligible subjects.

Review regulatory documents.

Accountability and inventory of medical devices and / or investigational products / drugs.

Verify and review 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 offer suggestions for improvement.

Complete monitoring reports and follow-up letters, which includes providing summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

Master's degree in a health-related field.

Willingness to travel 60-80% nationally.

Familiarity with Microsoft Office.

CRA certification completed as per DMC 15 / 11 / 2011.

Fluency in English and Italian.

Strong communication and presentation skills are 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 a scientific and disciplined approach.

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 the next steps.

EO / AA Employer M / F / Disability / Vets

J-18808-Ljbffr