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

Design, execute, oversee, and interpret experiments in partnership with other team members. Independently draft, review, and finalize both technical protocols and scientific reports while interacting in a cross specialty environment. Help determine process parameters range for cell culture and downstream processing to optimize PSC starting material yield and quality in a

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

Lead and manage multiple commissioning / qualification / validation activities performed at facility with minimal supervision. Equipment Qualification / Re Qualification (IQ, OQ, PQ) for process equipment, QC equipment, packaging equipment, clean utilities. Cleaning Verification / Validation studies for transferred products. Media Fills / process simulations protocols. En

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

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

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

You are an expert facilitator you open doors, foster communication, and bridge the gap. In this role, you will operate as the subject matter expert on reimbursement, access, and coverage issues affecting the clients product. Educate HCPs and their staff on matters related to reimbursement, access and coverage to facilitate appropriate patient access. You will Analyze acce

A unique opportunity is available in the Van Aelst and Lukey groups at Cold Spring Harbor Laboratory (CSHL) for a highly motivated and creative postdoctoral researcher, with strong experimental and analytical skills, to investigate metabolic interactions in the brain tumor microenvironment. You will become part of a multidisciplinary team of basic researchers studying gli

You are an expert facilitator you open doors, foster communication, and bridge the gap. In this role, you will operate as the subject matter expert on reimbursement, access, and coverage issues affecting the clients product. Educate HCPs and their staff on matters related to reimbursement, access and coverage to facilitate appropriate patient access. You will Analyze acce

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

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

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for

Postdoctoral position in cancer neuroscience The Trotman Lab at Cold Spring Harbor Laboratory is seeking applications for postdoctoral candidates with a strong background in neurobiology. We study lethal metastatic cancer. The project aims to define how peripheral nerves in the metastatic tumor environment interact with cancer cells and affect progression, therapy and dis

Conde Nast is a global media company producing the highest quality content with a footprint of more than 1 billion consumers in 32 territories through print, digital, video and social platforms. The company's portfolio includes many of the world's most respected and influential media properties including Vogue, Vanity Fair, Glamour, Self, GQ, The New Yorker, Conde Nast Tra