Clinical Research Associate - Entry (Home-Based)

What can Medpace offer you?

• Flexible working conditions – Opportunity to work from home and flexible working hours

• Visa sponsorship & transfer for qualified candidates already based in New Zealand

• Annual Merit increases

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 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.

• No metric for minimum required days on site per month.

• Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager

• Airline club allowance

• Casual Dress Code

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

• Bachelor's degree in a health or science related field;

• Knowledgeable about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.

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 g...