- Merck & Co. (Rahway, NJ)
- … Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial Compliance , Clinical Trial Management, ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Eisai, Inc (Nutley, NJ)
- …company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory standards. The Head of Clinical Operations leads ... function in the execution of all aspects of end-to-end clinical trials with the utmost compliance and quality consistent with Good Clinical Practice… more
- Merck & Co. (North Wales, PA)
- …Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial Compliance , Clinical Trial Management, ... the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position,...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (San Francisco, CA)
- …Skills:Budget Development, Business, Clinical Supply Chain Management, Clinical Trial Management, Compliance Frameworks, Cross-Cultural Awareness, Decision ... DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will streamline… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.GxP Quality System knowledge, ... systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ... ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Research & Development Division portfolio of clinical trials. -GCS is accountable for the planning, sourcing,...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.Knowledge of cGMP regulations ... systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience.The AVP will also be responsible… more
- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. The Executive Director, Global Clinical Development resides within the Oncology at Eisai. This Executive Director will lead ... franchise programs, and will be the clinical group leader for the ongoing and planned development...across teams, to accomplish critical milestones across programs in compliance with Eisai's SOP's and regulatory guidelines.Direct program level… more
- Eisai, Inc (Nutley, NJ)
- …for Good Clinical Practice (GCP) oversight, and for assuring the compliance of projects, products and programs with Eisai's Standard Operating Procedures (SOPs), ... your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality...you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for design, delivery… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. The Clinical Trial Assistant will support all phases of clinical study activities (feasibility, ... start-up, conduct and close-out) under the direction and supervision by study Clinical Operations Lead(s). Plans, support, creates, and communicates clinical … 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
- EmblemHealth (New York, NY)
- … recommendations/interventions to prescribers and interdisciplinary care teams. Ensure maintenance and compliance with clinical standards of the CMMP and MTM ... functions. Aid in the evaluation and maintenance of formulary set-up based on clinical requirements, compliance with regulatory bodies, and P&T rules. Other… more
- New Story Schools (Wyoming, PA)
- …development for staff, while ensuring adherence to best practices in classroom-based clinical care and intervention. Compliance & Safety Practices: Uphold FERPA ... Job Title: Clinical Director Location: Wyoming, PA 18644 Employment Type:...in a supportive school environment. Your Role as a Clinical Director: Clinical Leadership & IEP Alignment:… more
- Glaukos (Aliso Viejo, CA)
- … throughout study processes. Contribute to Process Development : Collaborate with Clinical Compliance to refine and develop SOPs and other department ... with development and writing of study protocols. Ensures protocols are in compliance with appropriate regulatory requirements and clinical operation written… more
- The University of Chicago (Chicago, IL)
- …is supported by five service units: Human Subject Protection (IRB); Research Compliance ; Clinical Research Operational Excellence; Clinical Research ... Department BSD OCR - Clinical Research Incubation About the Department The Office...operations and enable collaboration across the enterprise while promoting compliance and human subject protection. To do this, the… more
