- Merck & Co. (North Wales, PA)
- …and key strategic engagements. This includes the ability to:Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability ... the protocol in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and… more
- Merck & Co. (Rahway, NJ)
- …tactical/scientific mentorship to other clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP ... the protocol in collaboration with Data Management/Programming. Collaborating cross-functionally to monitor clinical data -to ensure quality, completeness , and… more
- Eisai, Inc (Nutley, NJ)
- …role ensures studies are conducted efficiently, within budget, and in compliance with regulatory standards. The Head of Clinical Operations leads teams of study ... clinical operations function, ensuring compliance with GCP and regulatory standards.Develop and implement strategic vision and hands-on operational management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relationships with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs.Facilitate ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: Manage… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Pharmaceutical industry, with involvement in regulated clinical trials, clinical safety, pharmacovigilance included regulatory document reviewMust have at ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....years proficiency in ICH GCP Guidelines, US and European regulatory requirements for the conduct of clinical … more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (Omaha, NE)
- …and will work closely with freight forwarders, QA departments, USDA and other regulatory officers. Provide data to the Finance department so they can assign transfer ... efficient mode to transfer international productsMiscellaneous Export TasksTransfer pricing, research samples, Supplier show free goods, facilitate transfers between… more
- Merck & Co. (Rahway, NJ)
- …- Manufacturing division, Global Workspace and Enterprise Services (GWES) and our research laboratories, Global Clinical Development for Southeast and part of ... including supplier management, compliance, risk management, diversity spend, and stakeholder management. Monitor key suppliers through a set of agreed KPIs and… more
- Eisai, Inc (Phoenix, AZ)
- …customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory /compliance ... is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …cross-functionally with multiple functions and groups throughout the US organization, Clinical development, Research & Early Development, other affiliates, and ... (MAPA), Customer Engagement and Integrated Solutions, Commercial Excellence, Legal, Regulatory Affairs, Compliance and other relevant NNI departments to ensure… more
- Eisai, Inc (Boston, MA)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... exceed sales objectives. This will be accomplished by conveying complex clinical information to customers and key stakeholders regarding FDA-approved indications of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …cross-functionally with multiple functions and groups throughout the US organization, Clinical development, Research & Early Development, other affiliates, and ... Market Access and Public Affairs (MAPA), Field Sales, Commercial Excellence, Regulatory Affairs, Integrated Customer Engagement, Global and other relevant NNI… more
- Mount Sinai Hospital (New York, NY)
- …The Project Manager II will oversee the entire portfolio of Investigator-Initiated Clinical Trials (IICTs)/ Clinical Research Sponsor Collaboration (CRSC) ... implementing, and overseeing comprehensive training programs for new staff within the clinical research teams. This role ensures that new employees are… more
- Edwards Lifesciences Corporation (Dallas, TX)
- …Join us and be part of our inspiring journey. We are searching for a Senior Clinical Research Monitor to join Edwards Aortic Field Monitoring team. As a ... Senior Clinical Research Monitor , you ensure... trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Develop and… more
- Hackensack Meridian Health (Hackensack, NJ)
- …mission to transform healthcare and serve as a leader of positive change. The Clinical Research Coordinator is responsible for data entry and query management, ... to institutional and protocol requirements while maintaining data integrity for all assigned clinical research studies. Responsibilities A day in the life of a… more
- Samsung Research America (Mountain View, CA)
- …strategy and management, clinical expertise, partnerships, UI/UX design, usability research , clinical research and validation, software development, AI ... following applicable health and safety principles and practices Provide Support to Clinical Research Organization (CRO) during planning and execution of … more
- Duke University (Durham, NC)
- …Occupational Summary Participates in or leads day to day operations of clinical research studies conducted by principal investigator(s) at Duke Medicine; ... involved in the collection, compilation, documentation, and analysis of clinical research data. May oversee the work...and supervise the activities of other licensed and unlicensed research staff. Monitor and initiate corrective action… more
- University of Kansas Medical Center (Kansas City, KS)
- …or equivalent demonstrated experience. Certifications/Licenses: Certification in Association of Clinical Research Professionals (ACRP) Certification in Society ... Description: Key Roles and Responsibilities: Lead large and complex research project applications for KUMC Monitor adherence...of Clinical Research Associates (SOCRA) Certification in Research Administrators… more
- PatientIQ (Chicago, IL)
- The Director of Clinical Research Success will report directly to the VP of MedTech and will be responsible for overseeing the success and satisfaction of our ... study growth within these partnerships, and reducing customer churn. The Director of Clinical Research Success will be a strategic thinker with in-depth… more
- Pennsylvania Medicine (Philadelphia, PA)
- …mission of providing the highest level of care to patients, conducting innovative research , and educating future leaders in the field of medicine. Working for this ... leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn Medicine, someone… more