Clinical Research Associate - All Levels

Medpace; Ciudad Autónoma de Buenos Aires; Presencial; ARS 43.552.000 - 72.588.000; Jornada completa

Descripción de la vacante

A global clinical research organization in Buenos Aires is seeking a Clinical Research Associate to conduct clinical trials and monitor research sites. This role requires a Bachelor’s degree in a health or science related field and excellent communication skills in both Spanish and English. Medpace offers competitive compensation, a dynamic working environment, and opportunities for professional growth.

Servicios

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Company-sponsored employee appreciation events

Formación

• Experience in clinical monitoring preferred.
• Proven track record of clinical patient management.
• Excellent communication skills in Spanish and English.

Responsabilidades

• Conduct qualification, initiation, monitoring, and closeout visits.
• Communicate with medical site staff including coordinators and physicians.
• Verify adequate investigator qualifications and resources.

Conocimientos

Clinical monitoring

Verbal and written communication in Spanish

Verbal and written communication in English

Educación

Bachelor’s degree in a health or science related field

Descripción del empleo

Overview

Join Medpace in Buenos Aires! The Clinical Research Associate at Medpace offers an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background who want to explore the research field, travel throughout Argentina, 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 varied backgrounds in medical and other science-related healthcare fields.

PACE – MEDPACE CRA TRAINING PROGRAM

No clinical experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other professionals achieving CRA Excellence:

• 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.

UNEXPECTED REWARDS

This role will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

• 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 and opportunity for significant travel bonus

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff
• Verifying 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
• 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
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
• Completion of monitoring reports and follow-up letters, including summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications

• Bachelor’s degree in a health or science related field
• Experience in clinical monitoring preferred
• Proven track record of clinical patient management, protocol, CRF, ISF preparation and TMF documentation reconciliation
• Excellent verbal and written communication skills in Spanish and English
• We kindly ask to send applications in English

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 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 diseases across key therapeutic areas. The work we do today will improve lives 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

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.