- University of Colorado (Aurora, CO)
- …Performed** **_Entry Professional:_** + Assist with and oversee the day-to-day operations of clinical trials and studies + Manage and conduct moderately complex ... practitioner, laboratory, radiology, pharmacy) + Identify, screen and consent potential study participants. Interact with clinical staff to confirm eligibility… more
- Merck (Rahway, NJ)
- …Laboratory Practice (GLP) studies . The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study ... and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory...research or similar research role. + Experience in a clinical study related role. **Required Skills:** Accountability,… more
- University of Utah (Salt Lake City, UT)
- …and operational capacity. + Coordinates technical and administrative details involved in research or clinical studies . + Exposure to study the development of ... studies while- assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …for global late phase studies * Coordinates review of interim/final clinical study reports.* Ensures effectiveness of site budget/contract processes + ... Operations team based in Santa Monica as a Senior Clinical Trial Manager, specializing in Late Phase studies...consents, case report forms, monitoring plans, investigator brochures, and clinical study reports.* Develop and Maintains … more
- J&J Family of Companies (Danvers, MA)
- …looking for a strong leader to support the development and design of Abiomed's global clinical studies with the focus on sound clinical evidence generation ... use of Abiomed products. The Principal Clinical Research Scientist will oversee clinical studies within the Clinical and Regulatory Affairs department.… more
- University of Colorado (Aurora, CO)
- …with and oversee the day-to-day operations of clinical trials and studies . + Obtain study subject's medical history and current medication information, ... manner. + Adhere to research regulatory standards and maintain detailed records of studies to ensure compliance with all requirements, study protocols, and… more
- University of Utah (Salt Lake City, UT)
- …Summary** **Job Summary** Coordinates technical and administrative details involved in a clinical or research study . Assists the Principal Investigator in ... the successful implementation and completion of protocols and procedures. Oversees clinical trials and studies related to Pediatric Neuromuscular research… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …study plans reviews + Participate in the review of Regulatory Documents ( Clinical Study Protocol, Investigators Brochure, Informed Consent Form, Clinica ... + **Provide quality oversight on the conduct of the clinical studies ** + Perform periodic quality reviews...** + Initiate the Quality Risk Assessment for every clinical study + **Qualification and periodic assessment… more
- Lilly (Indianapolis, IN)
- …lIT proposals and publications, as requested. + Contribute to global alignment of Phase 3b/4 clinical studies (and Phase I and II studies where applicable) ... 3b/4 studies (and phase I and II studies where applicable), as well as non- clinical ...product. + Responsible for the scientific training of the clinical study team. + Acts as scientific… more
- Bristol Myers Squibb (Madison, NJ)
- …across the internal and external network * Manages Phase 2 to Phase 3 clinical studies , with demonstrated decision-making capabilities * This role will include ... Delivery Team (SDT) and key member of the Clinical Development Team (CDT) * Study -Leader with...late clinical development needs and adequacy of clinical studies leading to registration **Qualifications &… more