Independent Contractor / Freelance - Clinical Research Associate (CRA)

Medpace, Inc.; São Paulo; Remote; BRL 120,000 - 180,000; Full time

Job summary

Medpace is seeking to add an experienced remote Independent Contractor for the position of CRA to our team in Brazil. The Clinical Research Associate at Medpace is offering the unique opportunity to have 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 Brazil, and be part of a team bringing pharmaceutical and medical devices to market -

Qualifications

• Bachelor's degree in a health or science field is required.
• 5+ years of clinical monitoring experience.
• Willingness to travel nationwide within Brazil.
• 6–12 month contract availability.
• Proven experience in CRF, ISF, and TMF documentation.
• Excellent verbal and written Portuguese and English.

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, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Skills

Clinical monitoring

Travel willingness

Portuguese & English communication

Education

Bachelor's degree in health or science

Job description

Job Summary

Medpace is seeking to add an experienced remote Independent Contractor for the position of CRA to our team in Brazil! The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development.For those withmedical and/or health/life science interest and backgroundwho want to explore the research field,travel throughout Brazil, and be part of a team bringing pharmaceutical and medical devices to market -this could be the right opportunity for you!

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, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

***We kindly ask that you submit your application in English***

• Bachelor's degree in a health or science related field is required;
• 5+ years of experience in clinical monitoring required;
• Willingness to travel nationwide within Brazil;
• Availability for a 6-12 month contract (term to be defined upon discussion);
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF and reconciling TMF documentation; and
• Excellent verbal and written communication skills in Portuguese and English

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.