Experienced Clinical Research Associate (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 FASTPACE® - A ccelerated, tailored training program based on your experience 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 and with at least 2 to 5 years of experience in clinical monitoring; 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...

Summary and match are AI-generated; verify details on the original posting.

Listed via Himalayas. All sources