Medpace
If you are looking for a stable, consistently, rapidly, developing CRO, Medpace is a great place for you! We are currently seeking full-time, home or office-based Clinical Research Associates to join our energetic Clinical Monitoring team in Hungary. We offer an exciting career where you can grow further, using your current and previous expertise. The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the development of medical therapeutics, in different, including rare diseases, cell and gene therapy, areas. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields, including but not limited to; Registered Nurses, Dieticians, Pharmacists, Faculty of Science Graduates and Research Assistants. An extensive training program provides the platform to effectively and confidently carry out your duties, the Medpace unique way.
Responsibilities
Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow‑up;
Assess patient recruitment and retention;
Lead CRA activities if eligible;
Mentoring and training Junior colleagues if eligible.
Qualifications
Minimum of a bachelor of science in health‑related field, MD or equivalent;
2+ years of independent monitoring experience;
Stable career history;
Broad knowledge of medical terminology and clinical patient management;
Basic knowledge of drug therapy techniques and clinical research methodologies;
Fluency in English and Hungarian;
Valid drivers licence.
Medpace Overview Medpace is a Global, 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 6,000 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 environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation and social events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for the next steps.
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Responsibilities
Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow‑up;
Assess patient recruitment and retention;
Lead CRA activities if eligible;
Mentoring and training Junior colleagues if eligible.
Qualifications
Minimum of a bachelor of science in health‑related field, MD or equivalent;
2+ years of independent monitoring experience;
Stable career history;
Broad knowledge of medical terminology and clinical patient management;
Basic knowledge of drug therapy techniques and clinical research methodologies;
Fluency in English and Hungarian;
Valid drivers licence.
Medpace Overview Medpace is a Global, 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 6,000 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 environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation and social events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for the next steps.
#J-18808-Ljbffr