Experienced Clinical Research Associate
Vor 2 Tagen
Job SummaryWhat can Medpace offer you? Flexible working conditions – Opportunity to work from home and flexible working hoursVisa sponsorship & transfer for qualified candidates already based in AustraliaCompetitive transportation allowanceAnnual Merit increasesVariable Compensation Bonus Plan – Lucrative bonus calculated directly from the number of visits you doFast PACE – Accelerated, tailored training program based on your experienceNo metric for minimum required days on site per month.Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial ManagerAirline club allowanceCasual Dress CodeResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits for 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, ensuring good documentation practices are adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;Ensure that the investigator is enrolling only eligible subjects;Review regulatory documents;Manage investigational product/drug accountability and inventory;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, providing summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.QualificationsBachelor's degree in a health or science related field and at least 1.5 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 OverviewMedpace 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 all 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 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 environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
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