- Merck & Co. (Rahway, NJ)
- …(GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business processes. This includes defining and optimizing ... Technology.Develop &/or and manage process related artifacts (process maps, documentation , training content and role identification), ensuring alignment across… more
- Merck & Co. (Rahway, NJ)
- …(MW&D) Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance ... in public disclosure of clinical trials and their results, document disclosure, and data...disclosure, and data sharing with external researchers. The Executive Director in Medical Writing will be responsible for overseeing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross Functional Team ... collection of authorship agreements, financial disclosures and author approvalsEnsures documentation of compliance with authorship and publication guidelines as… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical Affairs' ... externally sponsored clinical research (ESR)...project teams.Committee Facilitation: Facilitate review committee meetings, ensuring comprehensive documentation of meeting outcomes, decisions, and action items. Coordinate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads ... new and updated Core Data Sheets, EU and US Documentation : As the project lead, Independently or through direction...3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …US, EU, Japan, and other global sites. These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory ... Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in other DSI governance process (DRF, G-PAD, GROC, GRSC etc.) Interfaces with clinical & pre- clinical groups, Regulatory CM&C and other appropriate group within ... Joint-GPT as applicable.Supervises the identification and compilation of required documentation for submission. Prioritizes workload as necessary.Keeps current with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... EU. Preparation of updated Core Data Sheets, and EU and US Documentation : Independently manages, prepares and implements regulatory documents (eg, USPI, annotated… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Job Summary: The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This… more
- Merck & Co. (Rahway, NJ)
- …Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving ... and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development.A… more
- VNS Health (Manhattan, NY)
- …interdepartmental quality improvement activities such as development and engagement, clinical review, clinical risk management, and patient satisfaction. ... care. Manages Health Plans quality improvement activities and assures quality clinical and non- clinical compliance with regulatory authorities. Works under… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …privacy, legal, compliance, IT security, etc.Responsibilities- In conjunction with the Director of Data Stewardship, Cataloging and Process, develop implement a data ... strategies for cleansing and standardizing data, with a focus on eg, clinical , product, and vendor data and Identify and rectify data anomalies, inconsistencies,… more
- Northwell Health (Lake Success, NY)
- **Req Number** 134398 Job Description Directs the activities of the Clinical Documentation Improvement (CDI) department. Facilitates modifications to clinical ... and medical records coding staff. Job Responsibility + Leads a Clinical Documentation group by communicating with and developing staff members, and building… more
- Catholic Health Services (Rockville Centre, NY)
- …Responsible for improving the overall quality and completeness of clinical documentation through self-direction and self-management. Facilitates clarification ... to the clinical documentation through extensive interaction with physicians, nursing staff, care providers, and coding staff to ensure that appropriate… more
- City of New York (New York, NY)
- …and Social Justice Initiatives, STI, and Viral Hepatitis. BHHS seeks a Clinical Advisor/Viral Hepatitis Director to provide technical expertise and support ... related HIV, STIs, and viral hepatitis in NYC. The Clinical Advisor/Viral Hepatitis Director will also provide...required to bring to your interview copies of original documentation , such as: - A document that establishes identity… more
- Win (Women In Need) (New York, NY)
- Title of Position: Clinical Director (LCSW/LMHC) FLSA Status: Exempt Department: Transitional Housing Reports to: Program Director Positions reporting to ... to $89,301 per year Purpose of the Position The Clinical Director is responsible for the programmatic...Conduct audits of the Uniform Client Chart and supporting documentation to ensure compliance with Office of Temporary and… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …ICH and GCP guidelines as well as SOPs regarding safety * Authors clinical sections of communications/ documentation for regulatory agencies and may participate ... The Associate Medical Director works with their supervisor and other members...others; provide input on potential disease areas/indications; and craft clinical experiments that corroborate or inform the biology for… more
- Moses/Weitzman Health System (Stamford, CT)
- **Job Description Summary:** **Job Description:** The Clinical Director , Child Guidance Center (CGC) is a critical position within Community Health Center, Inc. ... the supervision of the Chief of Behavioral Health. The Clinical Director , CGC will ensure efficient operations...oversight for staff's proper and timely completion of required clinical documentation , program statistics and outcome data,… more
- Vibrant Emotional Health (New York, NY)
- …depending on qualifications, internal equity, and the budgeted amount for the role. Clinical Program Director Vibrant (formerly the Mental Health Association of ... Job Title: Program Director Department: Youth and Family Wellness Reports To:...NFL. Vibrant is seeking an exceptional candidate to implement clinical and administrative expertise for the Youth & Family… more
- Colgate-Palmolive (Piscataway, NJ)
- …your career a reason to smile and join our global team! We are seeking Director , Clinical Research with a strong background in designing and conducting oral ... are conducted in accordance with ethical standards and regulatory requirements. The Clinical Research Director will work with internal and external partners… more
