Medpace
Who We Are
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. We leverage local regulatory and deep therapeutic expertise across all major areas including Oncology, Cardiology, Metabolic disease, Endocrinology, CNS, Anti-infective, Rare Diseases and Advanced therapies, as well as Medical Devices.
Responsibilities
The Job
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol and local regulations across a variety of therapeutic areas;
- Communicate with the medical site staff including but not limited to coordinators and clinical research physicians;
- Verify adequate investigator qualifications, training and resources, as well as sites facilities, laboratories, equipment, and staff;
- Source documentation verifiction 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 and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol.
Qualifications
Your Profile
- You must have minimum 18 months of local on-site monitoring experience
- You will be willing to travel up to 60-80% of the time nationally
- A Bachelor`s degree in life science
- You will have strong communication and presentation skills
- You will be fluent in Bulgarian and English.
Medpace Overview
Medpace 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
- Hybrid work-from-home options (dependent upon position and level)
- Competitive PTO packages
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Flexible work schedule
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
Awards
- Recognized by Forbes as one of America’s Best Mid-size Companies in 2021, 2022 and 2023
- 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 next steps.
EO/AA Employer M/F/Disability/Vets
To apply for this job please visit careers.medpace.com.