Associate Director, Global Regulatory Labeling
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Flex position in Global Labeling, for a Global Labeling Product Leader for the Infectious Diseases/Vaccines/Global Public Health Therapeutic Area. The GLPL will have responsibility for: • The creation and maintenance of primary and derived labeling documents, and text for artwork for packaging components through the LWG and LC processes, as required • Ensuring quality of primary and derived labeling documents, and text for artwork for packaging components (e.g., alignment of labeling text with data, regulatory requirements, consistency (where appropriate) between labeling documents) • Contribution to and implementation of the global labeling strategy including the development of target labeling • Principal responsibilities include: • The creation and maintenance of primary (Core Company Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, EU Product Information (EUPI)) and derived (International Package Insert, labeling text for EU, US and international package components, and translations) labeling documents. Takes into account competitor labels when drafting labeling text. • Coordinates the development, revision, review and approval of primary and derived labeling documents including the Labeling working Group (LWG) and Labeling Committee (LC) activities related to these documents • Ensures dissemination of LC-approved CCDS, USPI, EUPI and derived labeling documents and supporting documentation • Ensures quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency (where appropriate) between labeling documents) • Contributes to and implements the global labeling strategy.Additional InformationSneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on click.appcast.io | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: ExecutiveIndustry: Pharmaceuticals
$137k - $235.75k
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...therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious... ...the right way.Reporting to the Senior Director, Global Pharmacovigilance Compliance, Standards... ...functional leaders (e.g., Clinical Operations, Regulatory Affairs, Quality Assurance, and the...SuggestedMinimum wageFull timeWork at officeLocal areaFlexible hours- ...Description:Johnson & Johnson Innovative Medicine is recruiting for a Director, Global Commercial Strategy, Respiratory in Horsham, PA.About... ...study development, product development decisions, and labeling that supports product strategy, commercial launch strategy and...SuggestedFull timeWork at officeLocal area
$137k - $235.75k
...Job Summary Purpose: The Associate Director, North American Regional Leader, is responsible for North American and global regulatory strategies for select projects spanning the oncology... ...the USPI, lead the development of NA labelling negotiation strategies, and development...SuggestedLocal areaImmediate startFlexible hours- ...Job Posting Locations:Horsham, Pennsylvania, United States of AmericaJob Description:We are searching for the best talent for a Director, Global Medical Affairs Strategy & Execution (Immunology) located in Horsham, PA. About ImmunologyOur expertise in Innovative Medicine...SuggestedFull timeFor contractorsWork experience placementLocal area
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$137k - $235.75k
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$142.4k - $224.1k
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...Innovative Medicine is recruiting for an Associate Director, Medical Communications & Scientific... ...of digital innovation across US and Global MAF networks, including creation, tracking... ...Veeva Systems and the Medical/Legal/Regulatory review processMust be highly...Full timeTemporary workWork experience placementLocal areaImmediate start- ...across the United States.Job Summary:The Global Cybersecurity Senior GRC Analyst plays a... ...the organization operates within its regulatory, legal, and compliance obligations while... ...assessments to evaluate potential risks associated with external partnerships and perform on...For contractors
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$142.4k - $224.1k
...customers' needs and strive to provide solutions to meet them. The Associate Director, US Pharma Payer Marketing, Enlicitide, will play a critical... ..., Integrated Account Management, Outcomes Research, Medical, Global Market Access (GMAx), DHH, and Policy to focus on ensuring...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- ...the Head of US Patient Advocacy & Government Affairs, as the Associate Director, US Patient Advocacy, you will develop and execute key advocacy... ...-building skills.About CSL BehringCSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused...Full timeWork at officeRemote work
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$137k - $235.75k
...while championing patients every step of the way.Learn more at Johnson & Johnson Innovative Medicine is currently seeking an Associate Director, Discovery Informatics to join our In Silico Drug Discovery team located in either Spring House, PA (preferred) or Cambridge,...Full timeTemporary workLocal areaRemote work- ...eDiscovery team, you will be responsible to support and grow a global team, own the strategy and direction for the people, processes,... ...response and eDiscovery analysts that will: Work closely with the Director, Security Operations to develop and implement a cybersecurity...Full timeWork experience placementImmediate start
- ...make a meaningful difference worldwide.Could you be our next Associate Director, Medical Affairs (Transplant and Immunology)? The job is in our... ...understanding, and strengthen scientific engagement in global markets (US and International). This position requires strong...Work at officeWorldwide3 days per week
$214.9k - $358.1k
Role SummaryThe Global Development Lead (GDL) represents Clinical... ...studies in support of worldwide regulatory submissions.The individual... ...Clinical Development Plan and associated protocol design documents.... ...activities including product labels, core data sheets, Investigator...Permanent employmentFull timeH1bLocal areaWorldwideVisa sponsorshipWork visaRelocation package2 days per week- The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical... ...Policy 70, Health Canada PRCI)Monitor emerging regulatory and industry trends and influence CSL's disclosure...Full timeWork at officeLocal area3 days per week
$137k - $235.75k
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$142.4k - $224.1k
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...submission.We are searching for the best talent for Senior Manager, Regulatory Program Management, Immunology.Purpose:The Regulatory Program... ...forward through the translation and distillation of overall global regulatory strategy to executable plans and the coordination of...Full timeLocal areaImmediate startWorldwide- ...Opportunity:In collaboration with the Lead Counsel, Global Clinical Development, as the Associate Director, Senior Counsel, Clinical, you will provide... ...Development function on a wide range of legal and regulatory issues. You will act as the primary escalation and...Full timePrivate practiceWork at office
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