Clinical Research Associate Entry
Vor 2 Tagen
Job SummaryWhat can Medpace offer you? Full-time employment and office-basedDynamic working environment, with varying responsibilities day-to-dayExpansive experience in multiple therapeutic areasWork within a team of therapeutic and regulatory expertsDefined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive transportation allowanceAnnual Merit increasesVariable Compensation Bonus Plan – Lucrative bonus calculated directly from the number of visits you doMEDPACE 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.ResponsibilitiesConduct 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 being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;Verify that the investigator is enrolling only eligible subjects;Review regulatory documents;Accountability and inventory of investigational product/drug;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, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.QualificationsBachelor's degree in a health or science related field;Prior 1 year of study coordinator experience is preferred;Willing to travel approximately 60-80% to locations nationwide is required, or less if remote/virtual visits;Strong communication and presentation skills;Must be detail-oriented and efficient in time management.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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