- Genmab (Princeton, NJ)
- …Role The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within ... Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group. You will oversee the implementation of submission… more
- Genmab (Remote, OR)
- …that has given you a solid knowledge on clinical drug development and regulatory requirements. The work done by the Associate Director, Medical Writing ... to support the conduct of the clinical trials and regulatory submissions/filings. The Associate Director, Medical Writing may also serve as a document… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- …day is important to us.DOWNLOAD OUR CODE OF CONDUCT The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for Global RA submission ... is responsible.Must understand and be updated with current Global Regulatory filing requirements and eCTD structure.Collaborate with Strategists (Leads), Publishers… more
- Sun Pharma (Taro Pharma) (New Brunswick, NJ)
- Contract Manufacturing Associate Job SummarySupport Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality ... assessment and risk management fundamentals/tools.Strong knowledge of cGMP, QA/QC and regulatory compliance (US, EU and other regulatory requirements).Strong… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- Associate Director, Clinical Operations Sun Pharma Advanced Research Company Limited Princeton, New Jersey SummaryThe Associate Director, Clinical Operations is ... negotiation and Clinical Study Agreement finalization, Translations, EC and Regulatory submission, Site initiation etc.).Oversee, manage and assess vendor… more
- Sun Pharma (Taro Pharma) (Billerica, MA)
- Job SummaryThe Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product ... and testing of radiopharmaceuticals is strongly preferredStrong familiarity with regulatory / compliance environment (cGMP, GLP) associated with parenteral drug… more
- Sun Pharma (Taro Pharma) (Billerica, MA)
- …products, raw materials, stability lotsOversee and continuously improve FDA / regulatory compliant Quality System for QC laboratory systemPlan, direct and coordinate ... review, QC test review, and lot disposition activitiesSupport any regulatory inspections or internal/external auditsPerform review of release, stability, validation,… more
- Building and Land Technology (Stamford, CT)
- …the United States.BLT is a fast-paced growth-oriented company.Position Overview of the Associate General Counsel:As the Associate General Counsel at BLT, you ... advancement within Building and Land Technology. Key Responsibilities of the Associate General Counsel:Contract Management: Review, and draft various real estate… more
- Genmab (Remote, OR)
- …to fulfilling our purpose. The Role & Department The Senior Programming Associate / Programming Manager supports the development of new therapies by ensuring ... in tables, figures, and listings for decision making. The Senior Programming Associate / Programming Manager will provide support to the Lead programmer and… more
- Genmab (Millstone, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose. Associate Digital Product Manager, Global Drug Safety and Pharmacovigilance This person will be ... and Digital Technologies at Genmab! The Role: As an Associate Digital Product Manager in IT & Digital, you...it back to the business stakeholders. Solid understanding of regulatory guidelines and data standards is a plus Ability… more
- Gallagher (Las Vegas, NV)
- …encourage you to apply. Overview: We are seeking an exceptional Resolution Associate Workers Compensation Claims Supervisor who embodies a passion for developing and ... the program, enabling the mastering of new loss investigation techniques, regulatory requirements, and claim handling best practices. Organized and efficient, they… more
- Genmab (Princeton, NJ)
- …and authentic is essential to fulfilling our purpose. The Role The Associate Director will support the medical communications strategy and deliverables for Genmab's ... to inform strategy, new tools and maximize engagement. Collaborate with Legal, Regulatory and Compliance to ensure compliant and successful programs and activities.… more
- Fannie Mae (Washington, DC)
- …assessment.THE IMPACT YOU WILL MAKEThe Internal Audit - Quantitative Model Risk - Senior Associate role will offer you the flexibility to make each day your own, ... governance, risk and control environments, as appropriate.Understand model risk regulatory requirements, supervisory guidance (eg SR 11-7), model risk policy… more
- Gallagher (Missoula, MT)
- …policies, procedures, and standard methodologies in accordance with statutory, regulatory , and ethics requirements. * Document and communicate claim activity ... timely and efficiently, supporting the outcome of the claim file. About you: Ideal candidates for this position will have: * Claims Background: WC * Jurisdictional Experience: Montana * Active Adjuster's licenses: Montana WC Certification As a key member of… more
- Genmab (Princeton, NJ)
- …Products Maintaining a compliant state in Genmab's SOX and GxP regulatory environments Work effectively in a Software development environment leveraging agile ... and collaboration tools like Jira, Confluence, Gitlab, Smartsheet, SharePoint, Teams, Slack etc. Requirements: Bachelor's Degree in Computer Science or Management Information Systems with a concentration in Finance Minimum 8 to 10 years of experience deploying… more
- Genmab (Princeton, NJ)
- …and tactical operational plans aligned to the commercial and regulatory objectives. Excellent stakeholder management, concise written communication, ability to ... influence, clearly communicate and collaborate across an increasingly complex matrix environment. Strong understanding of all aspects of clinical drug development, with particular emphasis on clinical trial design, trial execution, and strong knowledge about… more
- Sun Pharma (Taro Pharma) (Princeton, NJ)
- …Data ManagementFLSA Classification: Manager's Job Title:Head of BDMDepartment Head Title: Associate VPDoes This Position Have Any Direct Reports?YesJob Description ... with internal team members, senior management, external experts and regulatory authoritiesAuthoring or directing input to key study-related documents produced… more
- University of Miami (Miami, FL)
- …and maintains accurate records related to medications and treatments as per regulatory bodies, policies, procedures and physician orders.* Communicates plan of care ... as well as the appropriate team members, ensuring compliance with all regulatory guidelines (ie, HIPAA).* Uses available resources to assist in discharge planning.*… more
- Kellogg Community College (Bedford, MI)
- …may be involved in some mildly unpleasant situations. Minimum Qualifications 1. Associate 's degree in human resources, business, or related field, obtained from an ... to ensure the continued compliance with ACA, year-end reporting and regulatory requirements. Essential Function: EMPLOYEE RELATIONS AND INVESTIGATIONS Description *… more
- Inova Health System (Falls Church, VA)
- …Allied Health ProfessionalStart Date: ASAPDuration: OngoingShift: daysEmployment Type: StaffThe Associate Medical Physicist position plays an integral role in the ... renovated medical equipment and imaging network. Cooperates and adheres to regulatory agencies (state and federal) in demonstrating compliance with applicable rules… more
