We are currently seeking a Postdoctoral Fellow in the laboratory of Dr. Helen Hou at Cold Spring Harbor Laboratory (), starting in Fall 2023 or Spring 2024. You will play a decisive role in the research program of an interdisciplinary lab with the latest technologies in neuroscience, studying how the brain controls movements and natural behaviors, including but not limite

Postdoctoral positions in cancer genomics, evolution and immunology The Westcott Laboratory at Cold Spring Harbor Laboratory is seeking applications for postdoctoral candidates to carry our experimental and/or computational work aimed at understanding how cancer coevolves with the immune system in mouse models and clinical colorectal cancer specimens. The research program

DETAILS This position develops, documents and executes pre market and post market clinical evidence strategies for medical devices across product platforms. Works with cross functional teams and key stakeholders to execute on clinical evidence strategies for specific products/product families. For established products in the EU market, writes post market clinical follow up

Manager, Regulatory Affairs North America (Hybrid) It's an exciting time to be part of IFF's Global Regulatory Affairs. This hybrid role requires presence in the office minimum of 1 day/week in the Holmdel, NJ location. As the Manager of Regulatory Affairs, you will be responsible for the regulatory compliance and conformity to customer requirements for fragrance products

Cold Spring Harbor Laboratory invites applications for a Research Technician in the laboratory of Dr. Hannah Meyer (https //meyer lab cshl.github.io/). The successful candidate will join an interdisciplinary team of computational and experimental scientists to study T cell development and auto immunity. The lab technician will assist members in the Meyer lab in a variety

Singular talents thrive as an Associate Director of Medical Writing with Caudex. We advocate. We captivate. We cogently demonstrate. We combine gravitas with that lightness of touch that only comes from genuine, deeply held mastery and passion. We're recognised leaders in our field because we make the extraordinary seem effortless. We are your people. You're a recognised,

Fully competent in one or more scientific/technical areas. Plans and conducts scientific assignments requiring mastery of specialized techniques. Responsibilities Key Accountabilities Essential Functions Applies scientific method and experimental design in problem solving. Uses scientific expertise to provide solutions to a broad range of difficult problems. Solutions are

Advance innovative technologies that transform sustainable raw materials to high value ingredients that modulate tastes and enhance authentic flavors through microbial fermentation and biocatalysts. Design and conduct lab scale process development to implement upstream discovery into pipeline. Conduct instrumental analysis (GC MS & HPLC) of flavor components in samples to

Lead clinical pharmacology activities related to study design, protocol development, study execution, reporting and interpretation of data. Conduct PK and PK/PD analysis . Work closely with pharmacometrics team members and provides input related to analysis and reporting of PK and PK/PD. Lead development of clinical pharmacology sections for regulatory filings including a

Do you have what it takes a competitive drive coupled with exceptional sales ability. In this role, you'll be autonomous in your own territory promoting tablets for one of the largest, leading generics companies in the world. The selected professional will be an integral part of a nationwide sales team developing and managing an assigned territory. You will Maximize new b

PDI is seeking a Clinical Scientist II Microbiology to conduct antimicrobial testing, method development, and develop the strategy, design, execution, and interpretation of clinical trials in support of early drug development. Primarily, the role supports new market launches with input across all facets of project progression including scientific insights, prototype asses

Independently designs and performs analytical methods to measure drug formulations by reverse phase and size exclusion chromatography under Good Laboratory Practices (GLP) guidelines. Participate in the development, qualification, and validation of new analytical methods. Maintains an organized and detailed notebook according to Good Documentation Practices (GDP) guidelin

Manage Regulatory Affairs, Advertising & Promotion and Compliance Group Manage the US RA Ad Promo, submission operations, labeling and compliance group staff, including objective setting and career development activities and motivate line reports to achieve shared and individual goals. Regulatory Leadership of Advertising and Promotional Materials Serve as subject matter

R esponsibilities for the Software Quality , Lead position include Identify and manage cross functional process improvement projects across the Quality Assurance organization ; Manage CAPA and deviation identification, tracking, follow up, and closure; E valuate and approve proposed changes of GxP and non GxP systems prior to implementation ; R eview and a pprove system r

The Clinical Trial Documentation Specialist position is based within our Clinical Operations group, and works with departmental management and the Principal Investigator in the implementation of project clinical trial protocols. Job Type Full Time Base Hours 9 00AM 6 00PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be a