- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and immune disorders.Summary This position supports the strategy for driving global Clinical Study Start-Up activities for PV Safety Operations. This position ... and electronic data capture (EDC) Safety report outputs, reviews clinical study protocols and the Clinical... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …immune disorders. **Summary** This position supports the strategy for driving global Clinical Study Start-Up activities for PV Safety Operations. This position ... and electronic data capture (EDC) Safety report outputs, reviews clinical study protocols and the Clinical... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- University of Colorado (Aurora, CO)
- …analysis, or regulatory) **Preferred Qualifications:** + Prior experience with study startup , including startup for industry-sponsored clinical trials + ... 00821154 - Requisition #: 33101** **Job Summary:** **Key Responsibilities:** Study Startup 45% + Independently manages with..., targeting ~25 billable hours per week across all studies . + Other duties, as assigned by manager… more
- Boehringer Ingelheim (Ridgefield, CT)
- …reported and collected. + Participate in the study development and startup activities for both clinical trial and non-trial activities. Communicate complex ... terminology coding for all program types including but not limited to clinical trials, non-interventional studies (NIS), Investigator Initiated Studies … more
- University of Colorado (Aurora, CO)
- …regulatory agencies. Drafts regulatory documents and completes forms/paperwork. + Oversees study startup and regulatory processes. + Hiring, onboarding, and ... Clinical Science Program Manager - 33067...agencies. Drafts regulatory documents and completes forms/paperwork. + Oversees study startup and regulatory processes. + Hiring,… more
- Fresenius Medical Center (Waltham, MA)
- …highest level of quality possible. The CPM monitors and tracks the progress of clinical study activity at research sites ensuring compliance with all local, ... PURPOSE AND SCOPE: The Clinical Project Manager is a high...expertise in leading cross functional teams and driving the study planning, startup and execution. The CPM… more
- WuXi AppTec (CA)
- …management issues for their assigned trial + Proactively performs data management study startup activities including CRF/eCRF design, CRF annotation, developing ... **Overview** The Clinical Data Manager II performs ...coding, and quality control steps in accordance with WuXi Clinical Standard Operating Procedures + Ensures approved study… more
- Novo Nordisk (Lexington, MA)
- …and externally + Participate in the development of tools and metrics for monitoring clinical study progress and surveillance of key efficacy and safety data ... The Position We are looking to hire a Senior Clinical Project Manager (CPM). This is a... Program Lead when appropriate + Collaborate with the Clinical Program Lead and study team to… more
- University of Pennsylvania (Philadelphia, PA)
- …neurodegenerative diseases. The job functions include: Source documentation generation in study startup ; Contacting patients and caregivers to schedule research ... diseases. The job functions include: Source documentation generation in study startup ; Contacting patients and caregivers to...with 2-3 years of related experience in research and clinical study methodologies or equivalent combination of… more
- University of Michigan (Ann Arbor, MI)
- …coordinator (CRC) position may provide study coordination for multiple clinical research studies of any complexity. Coordinator experience and mastery ... and creative problem-solving skills across a wide variety of clinical studies . This position contributes to the...Safety Considerations 3. Investigational Products Development and Regulation 4. Clinical Study Operations (GCPs) 5. Study… more
- University of Michigan (Ann Arbor, MI)
- …a range of tasks associated with a variety of neurological clinical research studies . This position will provide study coordination for multiple clinical ... from a NeCTO Project Manager . This position provides study coordination for multiple clinical research studies of any complexity and in multiple… more
- Stanford University (Stanford, CA)
- …as part of a clinical trials research team and report to the Clinical Research Manager and various Principal Investigators conducting clinical research ... Clinical Research Coordinator Associate **School of Medicine, Stanford,...contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine… more
- Stanford University (Stanford, CA)
- …and/or manager /supervisor. The CRCA will support federal and non-federal clinical research studies including dermatological and investigative work in support ... Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies The CRCA will coordinate moderately complex aspects of… more
- University of Rochester (Rochester, NY)
- …at national meetings and interactions with study sponsors. + Interacts with study sponsors regarding study startup , ongoing study activities, ... study activities for large multiple site international clinical trials and core laboratories for FDA, NIH and...core laboratories for FDA, NIH and Investigator Sponsored Research clinical trials. Assists Manager in training of… more
- Lilly (Indianapolis, IN)
- …teams to understand the impact of design on speed to protocol approval and study startup . Identify and participate in opportunities to analyze experience and ... the programs in development, clinical research, and clinical program and study design. Thus, the...on the design of Phase II to Phase IV clinical programs and studies within the therapeutic… more
- Stanford University (Stanford, CA)
- …Under the supervision of ADRC principal investigator (Dr. Victor Henderson) and clinical research manager (Veronica Ramirez), main duties include in-person and ... Clinical Research Coordinator Associate (Hybrid) **School of Medicine,...contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine… more
- Takeda Pharmaceuticals (Columbus, OH)
- …**GOALS:** + Conduct data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/site feasibility and ... and establish a geographic country footprint and proposed sites for participation in a clinical study . + Leverage leading industry tools and data sources to… more
- Lilly (Indianapolis, IN)
- …teams to understand the impact of design on speed to protocol approval and study startup . Identify and participate in opportunities to analyze experience and ... the programs in development, clinical research, and clinical program and study design. Thus, the...on the design of Phase II to Phase IV clinical programs and studies within the therapeutic… more
- Bristol Myers Squibb (Cambridge, MA)
- …partnership with GDO protocol manager ; and collaborate with cross functional study team members + May support clinical development planning (collaboration ... Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. **Position Summary / Objective** +… more
- University of Pennsylvania (Philadelphia, PA)
- …supply management, track experimental drug and device use (accountability), assist in study startup procedures, and find creative solutions for various ... and modifications to the IRB, create source documentation, complete study invoicing, and lead trainings on studies ...with 4-5 years of related experience in research and clinical study methodologies or equivalent combination of… more
