- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Research Director (CRD) is the Clinical Operations lead in a country/cluster and is responsible-for execution of all Clinical ... collaboration.Oversight to ensure appropriate scientific and operational training for staff members. Clinical Operation Management : Ensures a single point of… more
- Merck & Co. (Rahway, NJ)
- …communicate with stakeholders at various levels, including cross-functional teams, senior management , external vendors, and clinical sites. Strong negotiation, ... Project Management Skills: strong knowledge of the principles of project management and clinical customer relationship management . - Technical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director , Device Technical Operations is a pivotal leadership role within the Device Development & Technology (DD&T) organization in our ... as well as combination product stewardship for inline products. The Executive Director will lead multiple functions in the department of approximately 50 employees,… more
- Merck & Co. (Rahway, NJ)
- …assets/biomarkers (including Regulatory, Commercial, Business Development, Project Management , Operations, Clinical Development, Statistics, Bioinformatics, ... Job DescriptionIn this Principal Scientist/ Director position within Translational Oncology, this team member...projects as needed, eg ordering samples, QC of incoming clinical trial biomarker results, assay/ data transfer troubleshooting,… more
- Merck & Co. (Rahway, NJ)
- Job Description Product Manager , Trial and Site Management Product Line - - Job Description - - Our Company Research Labs IT team partners with the Clinical ... and passionate P roduct Manager for Trial and Site Management P roduct L ine to own the product...- Work closely with software engineers , UX designers, data engineers, quality engineers and other product teams and… more
- Merck & Co. (Rahway, NJ)
- …standards of reference data and chemical nomenclatureLeading nomenclature and reference data projects or other data management tasksFacilitating timely ... or reference/master data standards (US and/or international)Experience with master data management systems, content, and processesExperience in master … more
- Merck & Co. (Rahway, NJ)
- …Dossiers for use by local subsidiaries in their local HTA submissionsDevelops supplementary clinical data package in close partnership with markets and HTA ... the guidance of a senior leader, a Senior Principal Scientist/Senior Director , has primary responsibility for developing value evidence strategies, and… more
- Merck & Co. (Rahway, NJ)
- …role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...Data Visualization, Machine Learning, Software Development, Stakeholder Relationship Management , Waterfall ModelPreferred Skills:Job Posting End Date:03/31/2025 *A job… more
- Merck & Co. (Rahway, NJ)
- … Visualization, Machine Learning, Software Development, Stakeholder Relationship Management , Waterfall ModelPreferred Skills:Job Posting End Date:03/31/2025 *A job ... Job DescriptionAssociate Director - Pharmacometrics, Quantitative Pharmacology and PharmacometricsThe Quantitative...modalities to drive portfolio impact from discovery through life-cycle management . The team is externally visible and continues to… more
- Merck & Co. (Rahway, NJ)
- … Visualization, Machine Learning, Software Development, Stakeholder Relationship Management , Waterfall ModelPreferred Skills:Job Posting End Date:03/28/2025 *A job ... therapeutic areas and modalities to drive portfolio impact from discovery through life-cycle management . The team is externally visible and continues to be at the… more
- Formation Bio (New York, NY)
- …communication and collaboration between internal teams, such as Clinical Development, Clinical Data Management , and Site Identification, and external ... to bring new treatments to patients faster and more efficiently.About the PositionThe Director of Clinical Trial Management is responsible for leading… more
- Merck & Co. (Rahway, NJ)
- … Visualization, Machine Learning, Software Development, Stakeholder Relationship Management , Waterfall ModelPreferred Skills:Job Posting End Date:03/31/2025 *A job ... therapeutic areas and modalities to drive portfolio impact from discovery through life-cycle management . The team is externally visible and continues to be at the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionUnder the guidance of a senior leader, a director has primary responsibility for developing value evidence strategies, and planning/managing real ... V&I goals. Responsible for study-related contracting, budgets, and vendor/partner management .Support market affiliates to develop local outcomes research plans,… more
- Merck & Co. (Rahway, NJ)
- …Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package for submission to Health Technology Assessment ... value evidence strategies for in-line and pipeline products. Obtain senior management approval of value evidence generation plans. Provide outcomes research… more
- Merck & Co. (Rahway, NJ)
- …such as manufacturing process development and validation, design control, risk management , material and molding, design validation to create and execute design ... verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal Responsibilities… more
- Formation Bio (New York, NY)
- …to bring new treatments to patients faster and more efficiently.About the PositionThe Director , Quality Management Systems plays a pivotal role in ensuring ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...of an effective, compliant and 'fit for purpose' quality management system (QMS) ensuring Formation Bio is in a… more
- Formation Bio (New York, NY)
- …development through regulatory submissions and approvals. Ability to collaborate cross-functionally with Clinical , Data Management , Programming, Data ... and improve trial efficiency. Regulatory & Cross-Functional Collaboration: Partner with Clinical , Data Science, Regulatory, and Business Development teams to… more
- Formation Bio (New York, NY)
- …including specification development, manufacturing, product release, stability programs, change management , and vendor oversight. The Sr. Director ensures ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...to patients faster and more efficiently.About the PositionThe Sr. Director , GMP Quality Assurance will lead the GMP QA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …early clinical safety for our Rare Disease/Specialty Medicine portfolio. SummaryThe Director , Clinical Safety, will be a product safety lead or part ... , and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection and management , important… more
- Formation Bio (New York, NY)
- …and continuous improvement among the Design team and its core partners (Product Management and Engineering, as well as scientific, data , and operational ... 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
