- Catalent Pharma Solutions (Somerset, NJ)
- …lean supply chains for individual studies or programs + Create initial study drug projections and supply plan for clinical supply needs throughout life ... **Senior Clinical Supplies Manager ** **Position Summary:** Catalent...and Catalent employee.** **The Role:** + Understand and translate clinical study protocol requirements into demand for… more
- Mount Sinai Health System (New York, NY)
- …per specifications of the protocol; and monitors test results, as appropriate Documents clinical study and therapy in patient's chart and all other databases ... **Job Description** The Clinical Program Manager provides clinical...research program. + Liaison with industry sponsors and CROs. Clinical Research Responsibilities: + Responsible for coordinating study… more
- Mount Sinai Health System (New York, NY)
- **Job Description** As the Clinical Trials Manager , you will coordinate and manage multiple clinical trial projects and protocols, including federally funded ... studies , investigator-initiated studies , and/or those from pharmaceutical companies. The ...management and leadership skills **Responsibilities** + Manages and coordinates clinical trial and related research studies conducted… more
- Mount Sinai Health System (New York, NY)
- **Job Description** We are seeking a Clinical Program Manager (CPM) to join a team of investigators and advanced practitioners who are dedicated to delivering ... events (ie serial vitals) and the accurate capture of clinical data for the purposes of the study and patient monitoring. + Teach, coach and mentor junior… more
- American Heart Association (New York, NY)
- …does your career. The American Heart Association has an excellent opportunity for a ** Clinical Data Manager ** in our **National Center** office. Location of the ... (including real world data) from multiple American Heart Association clinical trials, research studies and registries as well as other large external datasets.… more
- Actalent (New York, NY)
- Job Title: Clinical Study Manager Job...in the planning and execution of clinical studies . You will develop a cross-functional, integrated study ... aspects of the protocol are met. You will act as a project manager for the clinical study team, coordinating with internal stakeholders and overseeing CRO… more
- HSS (New York, NY)
- …Mission, you too can be part of our transformation across the enterprise. Clinical Research Manager - Industry Full-Time Summary: This position compliments and ... including but not limited to thematic area, industry, and pharmaceutical studies . The Research Manager facilitates multiple communication activities (oral,… more
- Terumo Medical Corporation (Somerset, NJ)
- Sr. Manager , Clinical Advisors Date: Oct 24, 2024 Req ID: 3739 Location: Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: Medical Affairs ... wherever we go next!** **_Advancing healthcare with heart_** **Job Summary** Senior Manager , Clinical Advisor is responsible for developing and implementing the… more
- Hackensack Meridian Health (Neptune, NJ)
- …mission to transform healthcare and serve as a leader of positive change. The ** Manager , Clinical Research Center Operations** is responsible for Clinical ... and regulations. **Responsibilities** A day in the life of a ** Manager , Clinical Research Center Operations** at **Hackensack Meridian** **_Health_** includes:… more
- Merck (Rahway, NJ)
- …Management Section of the GCS Planning organization. Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... and operational plans associated with the downstream activities of clinical supplies for their assigned studies . The primary function of the IM CSPM is planning… more
- Merck (Rahway, NJ)
- …the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... operational plans for all activities associated with clinical supplies for their assigned studies , which...+ Responsible and accountable for establishing the timelines for clinical supply needs per study and providing… more
- Merck (Rahway, NJ)
- …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary… more
- AbbVie (New York, NY)
- …extensions to CDISC + Oversee the creation of SDTM define.xml, annotated CRF and Clinical Study Data Reviewer's Guides for both FDA and PMDA submissions. + ... on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Manager , Clinical Data and Reporting Standards (CDARS) proactively participates… more
- Pfizer (New York, NY)
- … Scientist (CS) - Sr. Manager will support clinical epidemiology study execution for multiple studies for one or more vaccine programs. In collaboration ... Development and Life Cycle plans. Data generated by epidemiological studies is critical evidence needed to support clinical...informed consent documents and supports the preparation of other clinical study documents as needed. + Data… more
- Pfizer (New York, NY)
- …of efficacy (ESOE) and proof of concept (POC) studies . + *The OES Clinical Scientist (Senior Manager ) will also be mentored/obtain guidance from a more ... study clinician. Depending on experience, the OESD Senior Manager , Clinical Scientist may lead the development...and clinical subteams to meet enrollment and study delivery timelines. + The Senior Manager … more
- Pfizer (New York, NY)
- … Clinical Practices. + Thorough understanding of the processes associated with clinical study management and regulatory operations. + Ability to manage tasks, ... own projects within a team. + Serve as Data Manager for one or more clinical trials...by general users. + Ensure lessons learnt during the study are documented and shared with other study… more
- Deloitte (New York, NY)
- …retention + Knowledge of clinical data mapping, processing, use cases + Clinical study design functional experience + Data Management experience + Data ... connections that empower a digitally enabled, equitable future of health As a Manager you will lead and deliver small engagements, or components of large, complex… more
- Merck (Rahway, NJ)
- …CRD, the person is responsible for preparing, analyzing, negotiating, and revising Clinical Research related contracts and budgets through all phases of the contract ... negotiate, and execute required site agreements and associated budgets including Clinical Trial Research Agreements (CTRA), Master Clinical Trial Research… more
- Pfizer (New York, NY)
- …projects being reviewed JOB RESPONSIBILITIES + The CDR is routinely responsible for the clinical data review of one or more studies /programs, most often within a ... role is distinctly different from that of the Data Manager in that review tasks include both point-to-point data...+ Provides data review subject matter expertise support for studies , as needed, within Clinical Sciences group.… more
- Pfizer (New York, NY)
- …responsibility for all Data Monitoring and Management (DMM) activities and interact with Clinical Data Scientist at study level for deliverables. + Serve as ... of all phases of clinical trials and ability to assess and determine study requirement from protocol review + Working knowledge of clinical research, Food… more