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Jobs in Budapest, HUN - Covance

Clinical Research Assistant Senior Clinical Project Administrator
Covance  - Budapest, HUN
Clinical Research
Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career. If you prefer to speak about this job directly with a recruiter, please feel free to contact me at https://www.linkedin.com/in/krzysztof-orzechowski/ Location: office-based (B ...
Manager, Site Contracts
Covance  - Budapest, HUN
Clinical Research
About the Job Responsibilities/Duties : - Direct and/or indirect line management responsibility for Site contract staff, including without limitation recruitment, training, allocation, supervision, utilization and performance review of assigned personnel. - Independently, or with limited guidance, supervise Site contract staff in performance of their day to day wor ...
Talent Sourcing Recruiter
Covance  - Budapest, HUN
Human Resources
At Covance, your bold ideas will help bring innovative medicines to market and advance modern healthcare. You will map our most critical talent markets, compile competitive intelligence, research industry trends, and share perspectives on how to best compete in the external talent landscape. You will experiment with innovative marketing and creative sourcing tec ...
Start Up Manager
Covance  - Budapest, HUN
Clinical Research
The person will be on co-source in one of top-5 pharmaceutical comanies employed as Clinical Operations Manager. Responsible for start-up activities, ongoing regulatory submission and will hold study budget on a country leve. About the Job: Within this position, you will have to: - Develop project specific plans for the GSS component of assigned studies ...
Senior Clinical Research Associate - Early Development
Covance  - Budapest, HUN
Clinical Research Associate
patients into the study - Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review - Monitor data for missing or implausible data - Ensu ...
Clinical Research Associate
Covance  - Budapest, HUN
Clinical Research Associate
As a Clinical Research Associate you will manage all aspects of study site monitoring according to Covance SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and m ...
 

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