- Taiho Oncology (Princeton, NJ)
- … Clinical Operations in a dynamic, supportive, collaborative, and global cross-functional environment. Position Summary: Under minimal supervision, leads and ... manages complex global studies to support the Clinical Development...randomization processes, if applicable, and subsequent efficient and effective data management. + Ensure compliance with and adherence to… more
- Boehringer Ingelheim (St. Joseph, MO)
- …with the TPP and in compliance with global regulatory guidance and corporate standards for data integrity and animal welfare. + May direct and oversee ... of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate...Ingelheim's high regard for our employees. The Senior Scientist, Clinical is responsible for the safety and efficacy in… more
- Merck (San Diego, CA)
- … Clinical Trial Compliance, Clinical Trial Management, Communication, Data Analysis, Ethical Standards , ICH GCP Guidelines, Medical Writing, Motivation ... trial team. + Leading medical monitoring team in review and interpretation of clinical data /medical protocol deviations in collaborations with the Clinical … more
- Sanofi Group (Swiftwater, PA)
- …the Job** The Global Medical Writing Franchise Head is part of the Vaccine Clinical Documentation group and will manage a global group of Medical Writers who ... well as internal standards . + Participate in the review of strategic clinical documents (eg protocol ID card, Common Technical Document) prepared by the team to… more
- Takeda Pharmaceuticals (Boston, MA)
- … Operations Program Lead(s): + Oversee the execution of studies in assigned clinical program(s) in compliance with quality standards (including ICH GCP, local ... accountable for external spend related to study execution. Works closely with Clinical Operations Program Leader(s), Global Program Management, and Finance to… more
- Amgen (Washington, DC)
- … trials) to optimize clinical operations. + Working knowledge of clinical trial lifecycle regulatory requirements and industry standards (eg GCP ICH ... Join us and transform the lives of patients while transforming your career. ** Global Development Transformation Director** **What you will do** Lets do this. Lets… more
- Sanofi Group (Morristown, NJ)
- …performance and development goals **Regulatory Responsibilities** + Ensures clinical data meets all necessary regulatory standards + Supports registrations, ... Committee preparation and participation + Ensures timely submission and dissemination of clinical data + Supports the planning of advisory board meetings… more
- University of Colorado (Aurora, CO)
- …of data and data quality. Identify and help solve gaps in data collection. + Adhere to research regulatory standards + Maintain detailed records of ... **Research Services Clinical Science Professional (Entry to Intermediate)** **Description** **University... research or related experience + Experience with electronic data capture systems (eg EMR or EHR and … more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …public health standards , you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP ... performance, and drive accountability across regions. + Analyze and interpret global sales data -direct and through distributors-to identify revenue opportunities… more
- ICON Clinical Research (PA)
- …and industry standards . You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout ... trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards . + Conducting site visits to assess site… more