- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Management:Plans and directs the conduct of Data Management activities for assigned projects/ studies through outsourcing (eg, study startup , study ... according to applicable Daiichi Sankyo and regulatory requirements.Functional Expertise:Reviews/approves clinical study related documents (eg, Protocols, Data… 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
- 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
- University of Utah (Salt Lake City, UT)
- …assure high quality clinical research. + Organize and ensure proper study startup and closure procedures that conform to institutional requirements. Ensure ... Details **Open Date** 04/29/2024 **Requisition Number** PRN38391B **Job Title** PS Manager , Clinical Research **Working Title** PS Manager , Clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Management: + Plans and directs the conduct of Data Management activities for assigned projects/ studies through outsourcing (eg, study startup , study ... Daiichi Sankyo and regulatory requirements. + Functional Expertise: + Reviews/approves clinical study related documents (eg, Protocols, Data Management Plan,… 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 ... patients. The Position We are looking to hire a Clinical Project Manager (CPM). This is a... Program Lead when appropriate + Collaborate with the Clinical Program Lead and study team to… more
- Hackensack Meridian Health (Hackensack, NJ)
- …healthcare and serve as a leader of positive change. The **Project Manager , Clinical Trials** develops and implements comprehensive workflows and project/patient ... **Responsibilities** A day in the life of a **Project Manager , Clinical Trials** at Hackensack Meridian _Health_...and reliable documentation, tracking, and reporting of all required clinical trial study and patient data and… more
- Walgreens (Deerfield, IL)
- …the Director, Clinical Site Operations, and functions as the direct manager for patient-facing site staff supporting assigned studies . This role supervises ... "An Equal Opportunity Employer, including disability/veterans". **Job ID:** 1397364BR **Title:** Manager Clinical Site Operations RWE Clinical Trials… 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)
- …a range of tasks associated with a variety of neurological clinical research studies . This position will provide study coordination for multiple clinical ... report directly to the NeCTO Manager . This position provides study coordination for multiple clinical research studies of any complexity and in multiple… more
- University of Pennsylvania (Philadelphia, PA)
- …much more. Posted Job Title Clinical Research Program Lead Job Profile Title Clinical Research Program Manager C Job Description Summary This Clinical ... directly oversee and manage day-to-day operations for federally-funded NIH and industry sponsored clinical research studies in the portfolio of PIs in the Penn… 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
- Stanford University (Stanford, CA)
- …related to helping establish and coordinating moderately complex aspects of one or more clinical studies . The Clinical Research Coordinator will join a ... Clinical Research Coordinator Associate **School of Medicine, Stanford,...primary contact with research participants, sponsors, and regulatory agencies.Coordinate studies from startup through close-out. + Determine… 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
- 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
- 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
- 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
