- Charles River Laboratories (Northridge, CA)
- …Certification (eg, ASQ certification in auditing, SOCRA, CRS or Association for Clinical Research Professional) highly preferred. Compensation Data The pay range ... * Perform internal and external supplier audits. * Manage the inspection/back room during regulatory or customer audits. * Review validation reports (IQ/OQ/PQ) *… more
- San Jose State University (San Jose, CA)
- …the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality ... experience in a medical device, pharmaceutical, In Vitro Diagnostics, and/or Clinical Research Organization ( CRO ) or a Ph.D. in a relevant discipline with 0-2… more
- Charles River Laboratories (Poolesville, MD)
- …the following duties: + Prepare and distribute animal diets, enrichment, and clinical treatments; collect and record physiological data (pulse, respiration, ... reinforcement and cognitive testing; assist in on-going behavioral testing and data collection. + Assist veterinarian or investigators with surgeries or specialized… more
- PsychoGenics (Paramus, NJ)
- Senior Project Manager **PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best ... disabling CNS and orphan disorders and reduce the attrition rate in clinical development. We are known for our cutting-edge translational approach to research,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …The incumbent will display high scientific and ethical standards. **KEY ACCOUNTABILITIES:** ** Data generation** + Contributes to the clinical strategy and leads ... key flagship programs, including the data generation plan which includes both clinical ...a minimum of 7 years total pharma industry experience. Clinical research experience within the pharmaceutical industry, CRO… more
- J&J Family of Companies (Horsham, PA)
- …or real-word evidence), study conduct and operations (eg, medical monitoring, medical data review/ cleaning, CRO and vendor partnering/ oversight), data ... Immunology Medical Affairs, the Medical Director, Dermatology, will serve as the clinical subject matter expert (SME) in the Dermatology TA, leading medical affairs… more
- Johns Hopkins University (Baltimore, MD)
- Under limited supervision of the Clinical Research Program Manager, **_Sr. Research Program Coordinator_** is responsible for study site activation and management, ... including regulatory review, site study team training, data monitoring and integrity management, patient enrollment, and overall project timeline management for the… more
- Johns Hopkins University (Baltimore, MD)
- Under limited supervision of the Clinical Research Program Manager, we are seeking a **_Sr. Research Program Coordinator II_** who will be responsible for study site ... activation and management, including regulatory review, site study team training, data monitoring and integrity management, patient enrollment, and overall project… more
- Eurofins (Tucson, AZ)
- …leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the...used by the department + Review and evaluate raw data for acceptability + Manages the day-to-day operation of… more
- Eurofins (Louisville, KY)
- …leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the...issues holding up resulting of patient result + Complete data entry for specimen orders into LIS + Follow… more