- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …Director of Clinical Operations serves as project lead for clinical studies . Oversees the clinical feasibility assessment, strategic planning, and operations of ... clinical trial programs or studies . Executes on these global programs or ...submission to regulatory authorities (eg, protocols, investigator brochures, clinical study reports). + Manages clinical timelines, budgets, and resources… more
- Takeda Pharmaceuticals (Boston, MA)
- …Development Plan (IGDP). Responsible for review of synopses, other relevant clinical study documents and critical Study Results. Provide leadership and oversight ... Clinical Science Head to provide strategic clinical input on assigned clinical studies . + Consistent with the Takeda R&D Oncology Therapeutic Area Unit strategy,… more
- Vitalief (New Brunswick, NJ)
- …week remotely. Responsibilities: + Under the direction of the Clinical Research Study Site Leader, this resource will be responsible for supporting mostly Medical ... Oncology interventional studies (phase I through phase III) - Solid Tumor,...prepare and implement new clinical trials, screens and enrolls study participants, and provides protocol-related clinical management to those… more
- Mount Sinai Health System (New York, NY)
- …chemists, and toxicologists to support ongoing investigations involving clinical studies , exposure science, studies using large administrative datasets ... (eg, Medicare, state health data), and ongoing longitudinal cohort studies based at Mount Sinai. Opportunities to develop new...PhD, MD) and should be highly motivated to the study of environmental health, including learning new methodologies in… more
- Boehringer Ingelheim (Fulton, MO)
- …the parasites. + For studies of parasites strains propagation or for other studies when requested, acts as study lead with all accountabilities linked to ... parasites and vectors containing parasites for the reliable performance of GxP studies (GSP, GCP) for the development of veterinary medicines by independent planning… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …including CRO and vendor selection and management/oversight. The CPM ensures that studies are delivered on time, within budget, and in accordance with regulatory ... The CPM may also be known as the Clinical Study Manager. **Responsibilities** * Manage and lead the day-to-day...* Manage and lead the day-to-day operations of assigned studies to ensure completion per established project team goals… more
- Bristol Myers Squibb (Princeton, NJ)
- …improvement initiatives, supporting strategic planning efforts. The Director, GTL leads cross-functional study teams and study vendors to ensure successful ... a pivotal part in driving delivery of registrational and non-registrational studies , with broad impact across therapeutic areas and global teams.… more
- University of Miami (Miami, FL)
- …informed consent process and completes eligibility verification for applicable studies .2. Establishes and maintains communication with study participants, ... participant recruitment and retention activities and assists in screening potential study participants for eligibility.2. Performs study procedures, routine… more
- University of Utah (Salt Lake City, UT)
- …clinical research studies ; and (3) assist the Principal Investigator and study team in achieving study integrity and objectives through the successful ... procedures. **Responsibilities** 1. Screen and recruit participants for clinical research studies . 2. Fully understand the informed consent process and obtain… more
- ThermoFisher Scientific (Greenville, NC)
- …of clinical studies from Final Protocol Concept Sheet to Clinical Study Report (CSR) and applicable results disclosure. The CTL provides operational expertise, ... within our PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across… more