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Richfield, Minnesota, United States
Pay posted by employer$19.00–$22.00 per hour
Join us as a Research Associate – And assist in the coordination of clinical trials, manage data and sample collection, support …
Illkirch-Graffenstaden, France
Job Overview Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, …
Remote, Belgium
… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …
Bucharest, Romania
… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Work with sites to adapt, …
Riyadh, Saudi Arabia
… a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You Should Have A Bachelor's degree in a health care or other scientific …
Warsaw, Poland
… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, …
USA CA - Irvine Laguna Canyon
Pay posted by employer$105,500–$168,800 USD
… CRF development, study tools) Ability to communicate and relate well with key opinion leaders and clinical personnel Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & …
Baltimore MD
Pay posted by employer$60,000–$70,000
We are currently seeking an extraordinary, highly motivated individual to join our Research and Development team, with a focus on development and evaluation of emerging technologies for tissue and …
Santa Fe, New Mexico, United States
Pay posted by employer$53,700–$111,800
… join IQVIA Laboratories to help make the extraordinary possible! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare …
Madrid, Spain
The Senior Clinical Research Associate II is responsible for the site management, site monitoring and close-out of assigned clinical trials …
Remote, Netherlands
Join Us as a ( Senior) Clinical Research Associate in our client dedicated FSP team - Netherlands. Make an Impact at the Forefront of Innovation We have …
Remote, Belgium
Join Us as a ( Senior) Clinical Research Associate in our client dedicated FSP team - Belgium – Make an Impact at the Forefront of Innovation We have …
Warsaw, Poland
… of a Bachelors Degree in scientific discipline or health care. Experience of 1 year in on-site monitoring clinical trials . Good knowledge of, and skill in applying, applicable clinical research regulatory requirements …
Belgrade, Serbia
Job Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting …
Overland Park, Kansas, United States +2 locations
Pay posted by employer$71,900–$182,000
IQVIA is hiring Clinical Research Associates (CRA) at the 1 and 2 level. Candidate are required to have 6 months to 2 years of …
USA - Massachusetts - Boston (MA Parcel B Laboratory) +3 locations
Pay posted by employer$282,200–$444,200
The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for the strategic planning and directing …
Remote, Netherlands
Join Us as a Clinical Research Associate in our client dedicated FSP team - Netherlands. Make an Impact at the Forefront of Innovation We have …
West Australia, Australia +1 location
… making sure our food is safe or helping find cures for cancer. About the Role: Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …
Warsaw, Poland
… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing progress by tracking …
Kyiv, Ukraine
… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory …
Location reference: GeoNames (CC BY 4.0), normalized by Referizz.
