- Novo Nordisk Inc. (Plainsboro, NJ)
- …support optimization of access & reimbursement, clinical practice, product development and registration . The Director serves as a visible PED champion and subject ... and participates in US regulatory discussions and negotiations to optimize registration approval, product labeling & CFL promotion decisions Develops and maintains… more
- Genmab (NJ)
- …with Medical Director and reviewer of clinical and regulatory documents and registration dossiers (ie, protocol, ICF, IB, safety updates, study reports, regulatory ... submissions, etc.) to support registration and commercialization of the compound(s) Contributes in the development of case report forms (eCRFs), eCRFs completion… more
- Novo Nordisk Inc. (Boulder, CO)
- …Boards Assists with visitor logistics, meeting planning, meet & greet, pre- registration Actively supports internal teams, as appropriate, to assist with industry ... conference coordination, calendar management, oversee international and domestic travel working closely with dedicated travel partner Responsible for ensuring that high quality standards and efficient processes are followed Takes an active role in creating a… more
- Merck & Co. (South San Francisco, CA)
- …through the worldwide marketing application filing including supportive registration documents and presentations.Provide clear, timely communication and ... interpretation of study results to therapeutic area governance, functional area experts and development review committees.Contribute to assessment of internal and external opportunities identified by Business Development and Licensing.Interface broadly with… more
- Merck & Co. (Rahway, NJ)
- …to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration . Directors are leaders in the field of quantitative drug development, ... with a strong, integrated understanding of the strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute to… more
- Merck & Co. (Rahway, NJ)
- …to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration . Associate Directors are emerging leaders in the field of quantitative ... drug development, with a developing understanding of the strategic elements of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams of highly collaborative,… more
- Merck & Co. (Rahway, NJ)
- …a global regulatory pharmaceuticals team to create and maintain global registration dossiers in the Veeva Submissions platform.The Specialist's responsibilities will ... include:Creating global and country specific regulatory dossiers in the Veeva Submissions Platform.Assisting with the maintenance of global and country specific regulatory dossiers in the Veeva Submissions Platform. --Assistance with the conversion of the… more
- Merck & Co. (Rahway, NJ)
- …planning and execution of strategies for drug or vaccine product registration , commercialization and life-cycle management in R&D.Expertise in innovation development ... across biopharma and other science-based product industries with ability to drive innovative approaches and share cross-industry perspectives, new ideas, and best practices into new settings and environments.Demonstrated ability and expertise to analyze,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …list. Coordinate with Data Operations Team on coding dictionary set up, registration of dictionaries, and responsible for user acceptance testing specification and ... execution. Study Conduct: Responsible for adherence of coding of medical terminology and medications to Daiichi Sankyo coding conventions. Reviews and submits DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …science or engineering degree required; Licensed before a State Bar is required, registration before USPTO is preferred. Minimum of four - six years patent attorney ... experience in patent litigation is required, preferably in private practice. Experience in licensing and patent prosecution is preferred but not required. Effective time management skills. Ability to handle multiple projects simultaneously Experience with… more
- Merck & Co. (Rahway, NJ)
- …and product specification to support drug substance development and registration .Have a fundamental knowledge of synthetic (organic) chemistry.Have working knowledge ... of API development and commercialization.Have experience working with contract manufacture organizations and/or contract research organizations.Experience working in cross-functional teams.Current Employees apply HERE Current Contingent Workers apply HERE US… more
- Merck & Co. (Rahway, NJ)
- …molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, ... device, and manufacturing process.- Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively… more
- Merck & Co. (Rahway, NJ)
- …analytical development of candidates from the discovery interface, through first product registration . They will be responsible for a portfolio of Biologics programs ... (approximately 10-15 programs), and leading multiple Director lead Development teams, overall approximately 40-50 scientists. Strategic partnering with Biologics Analytical Research and Development method development GMP laboratories, complementary areas of… more
- Twist BioScience (South San Francisco, CA)
- …Form 8-Ks, the proxy statement and related documents, Section 16 filings, Registration Statements (S-1, S-8, and S-3), and Forms 10-Qs and 10-KsSupport Board ... and Committee meetings, including the drafting, preparation and review of Board meeting materials, minutes, and D&O questionnairesSupport Twist's annual stockholders meetingSupport Investor Relations by reviewing press releases, earnings releases, investor… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and drives the strategy for all Regulatory activities associated with the registration and support of new and approved drug products.Seeks and incorporate regional ... and functional RA strategy into a global strategy.Responsible for ensuring aligned global regulatory strategy is endorsed by GPT and other governance bodies.Serve as a leader of the GRT (Global Regulatory Team)The primary point of contact with Alliance… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …functionality. This role is also responsible for optimization of hub registration and associated acquisition strategy Content Strategy and Management: Developing a ... content strategy for the customer portal that aligns with user needs and organizational objectives. This includes identifying content requirements and partnering with brand/TA teams, Omnichannel Orchestration, Experience Operations, and agencies for enablement… more
- City of Detroit (Detroit, MI)
- Registration Specialist (Administrative Special Services - TASS) Print (https://www.governmentjobs.com/careers/detroit/jobs/newprint/4685736) Apply Registration ... + Questions Description DETROIT HEALTH DEPARTMENT NEIGHBORHOOD WELLNESS CENTERS ( REGISTRATION SPECIALIST) The Detroit Health Department is committed to addressing… more
- Dignity Health (San Luis Obispo, CA)
- …**Responsibilities** Employing excellent customer service skills the Patient Registration Specialist is responsible for ensuring a positive patient ... experience throughout the registration insurance verification benefit analysis and financial clearance process. Primary duties include appropriate patient… more
- CUNY (Brooklyn, NY)
- Enrollment Registration Specialist (Higher Education Assistant) **POSITION DETAILS** New York City College of Technology (City Tech) of the City University of New ... 58 associate and baccalaureate degrees, invites applications for the Enrollment Registration Specialist. As a member of the Registrar's office, the Enrollment… more
- Covenant Health Inc. (Knoxville, TN)
- Overview Patient Registration Specialist, Admitting & Registration Full Time, 80 Hours per pay period, Variable shifts Parkwest Overview: Parkwest is West ... as one of Tennessee's "Top 10" hospitals. Admitting & Registration : Our friendly and courteous registration staff is here to serve the patients' registration… more
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