- Merck & Co. (Rahway, NJ)
- …clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves ... spokesperson at clinical and development related meetings.- Working independently, the Program CSPM designs strategic and operational plans for all clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will ... collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Merck & Co. (Rahway, NJ)
- …experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Atherosclerosis… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Management resources, CROs, and vendors to ensure compliance with the program standards, Policies, SOPs, external/internal standards, Good Clinical Practices ... areas centered around rare diseases and immune disorders. Summary: The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary:The Associate Director, Oncology Value & Market Dynamics Training Manager is responsible ... to access for patients across our portfolio of products. The Associate Director will develop, in partnership with other key stakeholders, innovative… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to CDx project teams for the diagnostic, under the direction of the Global Program Teams (GPT) CDx representative for the therapeutic or under the guidance of the ... ensure successful implementation of the CDx and associated data collection. Oversees clinical trial sample testing activities and data capture to support CDx… more
- Merck & Co. (Rahway, NJ)
- …the application of cellular, molecular technologies and models to drive program decisions.Detailed understanding of translational and clinical research ... our newly created Precision Medicine and Diagnostics function. Reporting to the Associate Vice President ,Precision Medicine and Diagnostics, in this role, you will… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... products Track applications through FDA reviewing divisions Work with project associate on compilation of information and supportive documentation for FDA briefing… more
- Merck & Co. (Rahway, NJ)
- …regulatory submissions. -Under the general scientific and administrative direction of Associate Principal Scientist, and working in conjunction with internal and ... and inspections as required.Provide technical leadership in the assessment of program -specific cell bank processes, interpretations of cell bank performance, as well… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …QA RDPVQA, and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global Quality teams ... Project TeamsGOMA and Specialty MA Management teamsData Management/ Biostats Clinical Safety and PharmacovigilanceR&DVendors/ CROs/ third partiesHEOR/ RWEEpidemiology Legal… more
- Charles B. Wang Community Health Center (Manhattan, NY)
- Full-Time Clinical Program Associate - Manhattan Reports to: Clinical Operations Manager 268 Canal Street Manhattan, New York, 10013 United States ... Responsibilities : + Coordinate the on-site and off-site clinical programs and projects + Maintain the inventory of...for the first year of employment) + Employee Assistance Program + Tuition reimbursement for eligible employees, and +… more
- Merck (Rahway, NJ)
- …clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves ... spokesperson at clinical and development related meetings. Working independently, the Program CSPM designs strategic and operational plans for all clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will ... collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary… more
- Penn Medicine (Yardley, PA)
- …employees shape our future each day. Are you living your life's work? Clinical Services Associate (Medical Assistant) **Entity:** (CCA) /Penn Primary Care (PPC) ... that actively supports your career growth? If so, a Clinical Services Associate opportunity at Penn Medicine...Diploma/GED (Required) + Completion of an accredited Medical Assistant program (or higher level equivalent) required + OR 2… more
- Touro University (New York, NY)
- …model professionalism + Ability to balance flexibility while maintaining a high-quality clinical program + Excellent time management skills + Highly ... Practice and supported by the Assistant Professor for Clinical Practice, the Professional Development Associate (PDA)...or academic unit level + Experience in course or program design + Strong expertise in urban education +… more
- Sumitomo Pharma (Trenton, NJ)
- …Overview** We are currently seeking a versatile and experienced Senior Manager - Associate Director level scientist with strengths in clinical pharmacology, and ... will work across organization and functions and collaborate closely with program management, clinical development, PV, Biostat/Data Management, CMC,… more
- Bristol Myers Squibb (Princeton, NJ)
- …therapeutic areas. The ideal candidate will support early and late-stage clinical drug development across therapeutic areas by leveraging Quantitative Systems ... and a strong record of collaboration with discovery, translational, and clinical development teams are strongly preferred. Familiarity with immunology and relevant… more
