- Merck (North Wales, PA)
- …& Development (R&D) projects (data, analyses, tables, graphics, listings). + Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation ... and validate global programming standards and tools for the production of Study Data Tabulation Model (SDTM) datasets. + Design and develop complex programming… more
- University of Pennsylvania (Philadelphia, PA)
- …Unit (CRU)- Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations . The successful candidate ... to develop project plans and support day to day operations of clinical research proposals for their...Specialist, Billing Compliance staff, and Finance office to develop clinical trial budgets. Communicating any specialized study … more
- Merck (North Wales, PA)
- …to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication + Participation in internal and joint ... **Job Description** The Associate Vice President (AVP) has primary responsibility for...President will manage and oversee the entire cycle of clinical development, including study design, initiation, execution,… more
- Merck (North Wales, PA)
- … clinical documents including development plans, protocols, trial related documents, clinical study reports and background documents. + Interfaces with ... **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical...your employment may pose an undue burden to business operations , in which case you may not be offered… more
- Merck (North Wales, PA)
- …to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication + Participation in internal and joint ... of Clinical Scientists in the execution of clinical studies . + Work closely with a...in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects + Assist the Associate … more
- WCG Clinical (Princeton, NJ)
- …Thorough knowledge of current regulatory and GCP guidelines as they apply to clinical studies and WCG services/products. + Strong organizational and planning ... Senior Associate , Operations QA & Compliance (Remote)...Time - Regular **Description and Requirements** **ABOUT WCG:** WCG's clinical solutions are built on a foundation of best-in-class… more
- J&J Family of Companies (Titusville, NJ)
- …partner organizations (ie Quality, Drug Product Development, Analytical Development, Global Clinical Operations ). + Ensure TS&E activities are consistent with ... pharma/life sciences. * Experience with minimum one the following functions: clinical operations , logistics, distribution, operations , temperature… more
- Taiho Oncology (Princeton, NJ)
- …the outsourcing process from Request for Proposal (RFP) through contract execution for clinical studies and CMC projects as well as ongoing governance with ... meet the corporate goals. + Establish Preferred suppliers for clinical studies and other R&D categories and...of contracts. + Knowledge of internal disciplines such as clinical operations , data management, Pharmacovigilance Operations… more
- Bristol Myers Squibb (Princeton, NJ)
- …subject matter expertise and oversight on the IC process in support of clinical operations , including during audits and inspections. + Establish objectives, ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to...the pharmaceutical industry and 3-5 years of experience in clinical operations and/or Good Clinical … more
- Merck (West Point, PA)
- **Job Description** Our Company a global healthcare leader, is seeking an Associate Principal Scientist to join our collaborative, dynamic, and inclusive Laboratory ... discovery and in the GLP environment. On-site and hands-on study -related lab work will be a crucial part of...surgical modes in various preclinical species. Provide excellent preventative, clinical , diagnostic, and surgical care and services to a… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... individual will be responsible for TM and clinical biomarker activities to support drug development programs in...lead responsibilities such as serving as biomarker representative on study teams, setting up biomarker plans for individual trials… more
- Bristol Myers Squibb (Princeton, NJ)
- …late stage TM group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in multiple diseases in ... assume biomarker lead responsibilities, such as serving as biomarker representative on study teams, setting up biomarker plans for individual trials and ensuring… more
- Merck (Lower Gwynedd, PA)
- …Mesoscale, and/or cell-based functional immunogenicity assays preclinical and clinical regulated studies . + Method development, qualification/validation, ... and expanding your career. We are seeking a highly motivated Associate Principal Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism,… more
- Bristol Myers Squibb (Princeton, NJ)
- …information should be directed to the hiring manager.** **R1569291 Assistant/ Associate Biological Technician (H14/H24) or Biological Technician (H29)** **Shift:** ... - $38.14 H24 - $39.23 H29 - $42.61 **JOB SUMMARY** The (Assistant/ Associate ) Biological Technician performs semi-routine or diversified work that requires the… more
- Bristol Myers Squibb (Princeton, NJ)
- …The CTI Lead is responsible day-to-day Cyber Threat Intelligence (CTI) operations , to include collections management, analysis standards, quality control, and ... range of technical and non-technical internal customers such as security operations teams, information technology teams, enterprise risk management teams, and… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology and ... will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department within… more
- Penn Medicine (Plainsboro, NJ)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... Are you living your life's work? + Patient Access Associate + Hours: Friday and Saturday 11:00PM-7:00AM (8 hours...environment. Demonstrates willingness to meet the needs of departmental operations effectively as an individual and team member. +… more
- Merck (North Wales, PA)
- …Director/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates...product labeling as it relates to the use of study results in US promotion. Maintain current awareness of… more
- Merck (West Point, PA)
- …expanding your career. VAX Process R&D is responsible for the development and clinical manufacturing of Drug Substance (DS) and Drug Product Intermediates (DPI) for ... Process R&D organization, which enables modality-agnostic DS/DPI process development and clinical manufacturing for all of our company's pipeline. Applications are… more
- Merck (Trenton, NJ)
- …generation studies (LDG) with OR + Supports the Investigator-Initiated Study program + Leads talent review process and demonstrates follow-through on Development ... team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders...Brand and V&I Outcome Research Team leads to define clinical development plans and brand strategies for assigned TAs… more