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Firm Type: Law Firm, Experience: 3 Years, Job Overview: A law firm is seeking a Junior to Mid-Level Litigation Associate Attorney to join their team in Florham Park, NJ. The ideal candidate will have 3-6 years of litigation and/or employment law experience, outstanding academic credentials and the ability to work independently.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Associate Director will also have responsibility for ensuring consistent and appropriate implementation of global initiatives and messages within the US and Canadian markets, as well as regional external communications; stakeholder/media relations; public affairs/issues management; corporate brand; and, individual branded product communications.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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They also have highly-respected practices in insurance and reinsurance disputes, banking law, environmental law, employment law, family practice, tax and trusts and estates, corporate law, governmental affairs, public finance, public utilities, and real estate.
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Liaise and partner with U.S. and global colleagues across Corporate Affairs including State Government Relations, Federal Government Relations, Communications and Public Affairs and Patient Advocacy, Policy and Reimbursement and Global Media Relations to ensure aligned messaging and positioning to all key stakeholders.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Proclinical is seeking an (Associate) Director, Regulatory Affairs, Advertising & Promotion for a global pharmaceutical company with their location in New Jersey. (Associate) Director, US Regulatory Affairs, Advertising & Promotion - Permanent - NJ & MA.
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The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval conditions. Under the direction of Regulatory Affairs management, participate in drug development from early stage development through final formulation, ensuring compliance with principles of Quality-by-Design, cGMP, and FDA rules and regulations.
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The Associate Director of Medical Writing (MW) is responsible for managing MW and quality control (QC) activities in accordance with the Head of Regulatory Affairs in a timely, accurate, and efficient manner in compliance with company and global regulations, including ICH and GCP. The Associate Director, MW will work cross functionally with internal departments and external resources to author, edit, and provide project management support for clinical regulatory documents.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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With 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Associate Director, Brand Counsel will provide legal support and review of materials for commercial and medical affairs activities related to Insmed’s in-line rare disease respiratory product.
$220,200 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Associate Director/Director , a member of Shionogi’s Global Epidemiology and Real-World Evidence (GEE) team, is responsible for strategizing and generating real-world evidence using fit-for-purpose data to support global products at each stage of the product lifecycle.
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Provide strategic direction pertinent to CSPV Medical Affairs activities for internal QA team (global/ local), and not limited to: Global Project Team, Safety Management Team, Clinical Safety and Pharmacovigilance Medical Affairs, Companion Diagnostics/ Device Laboratories Vendors/ CROs.
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The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCP’s, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
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Medical Affairs, Legal, Regulatory, Finance, Market Access, Sales, Sales Operations. The Associate Director, US Marketing Product Lead, is responsible for supporting HCP marketing efforts in the U.S. market and driving a successful brand launch.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Under the general guidance of the Director Regulatory Affairs, Regulatory Affairs Associate plays a crucial role in ensuring the quality, and accuracy of drug product submissions to regulatory authorities.
$30 an hourPart-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The base salary range for the Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from :181,000-237,600. This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional teams including US medical affairs, marketing, market access global value and access teams, commercial to align strategies in customer research activities and development of external communication materials.
Full-timeExpandApply NowActive JobUpdated 19 days ago
affairs associate jobs in Basking Ridge, NJ
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