- Merck & Co. (North Wales, PA)
- …to the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review ... objectives.Serve as the liaison and manages correspondence with FDA's promotional review divisions Office of Promotion and Advertising Review (OPDP)/Advertising… more
- Merck & Co. (North Wales, PA)
- …aCRF; knowledge of Analysis Dataset Model (ADaM) and Analysis Data Reviewer 's Guide (ADRG) considered a plus.Excellent communication and interpersonal skills and ... ability to negotiate and partner effectively.Excellent written, oral, and presentation skills.Excels in technical writing, able to convert complex ideas and information into simple readable form.Strong project management skills; Manage at a program level;… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Associate Director, Global Medical Affairs (GMA) Oncology- Medical Content and Training ... is responsible for execution of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans and… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... training and oversight of the animal care staff, serving as a designated reviewer and voting member of the Institutional Animal Care and Use Committee (IACUC),… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Associate Manager as part of the Quality team based in Raritan, NJ. Role ... Responsibilities Manage the team responsible for drug product batch record review and drug product release practices.Develop positive relationships with the QA… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …as we work together to change lives for the better. The Position The Associate Director, Digital Content Strategy & Production reports to the Dir, Content & Channel ... Social Media Marketing and related recommendations for the NNI US website. The Associate Director supports the development and evolution of NNI's content strategy in… more
- Aequor (South San Francisco, CA)
- Job Title : Commercial Purchasing Associate Location : South San Francisco, CA (on-site) Duration : Until 09/30/2025 Context The Commercial Portfolio Organization ... (PO) requisition and invoice processing. Position Overview The Commercial Purchasing Associate will be responsible for creating POs and processing multiline invoices… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and strong collaborators, as we embark on shaping our future. The Position The Associate Director (AD), Executive Office serves as a key partner to the Executive ... government officials, etc. Drive and execute preparation for quarterly Business Review Meetings (BRMs) with Executive Management, ensuring internal content alignment… more
- Aequor (West Greenwich, RI)
- …procedures and products follow cGMP practices and other applicable regulations. Performs review and approval of cGMP processes, procedures, documents and records. ... Review logbooks, batch records, attachments, work orders, and other GMP documentation. Ensure that deviations from established procedures are documented per… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary: The Associate Director, Regional Marketing Conventions & Field Programs will be ... while ensuring adherence to DS policies and procedures. The Associate Director, Regional Marketing Conventions & Field Programs is...areas.Meet with Sales Leadership on a regular basis to review processes and gain insight of the field needs… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leads dose-escalation meetings; Performs quality assessment with Delivery Lead eg review Tables/Listings/Graphs before database lock and quality check of data; Works ... with BD&O to ensure SAP updateExternal collaboration: Consults with internal experts and external KOLs, Ad Boards for protocol development; Provides input on CRO / ARO Statement of Work and Budget; Establishes effective communication between CRO / vendors /… more
- Aequor (MA)
- …clinical materials for use in clinical trials Perform lot release Quality Review of manufacturing and quality control records to ensure compliance with ... that all requirements, as stipulated in the appropriate QTA, have been met. Issue/ Review documentation, ie Deviations, CAPAs, OOS (out of spec) etc., as they occur.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director, Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 clinical ... study start up (eg, database set up)Lead medical monitoring team in review and interpretation of clinical data/medical protocol-deviations in collaboration with the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and external ... projects and other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our Research & Development… more
- Merck & Co. (North Wales, PA)
- …the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, ... and high-quality data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the design, development, and… more
- Merck & Co. (North Wales, PA)
- …responsible for planning and ensuring the accuracy of Statistical Review Aids submitted to regulatory agencies.Participates with management in discussions ... with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.Involved in research activities for innovative statistical methods and applications in clinical trial development.Mentors and guides… more
- Eisai, Inc (Baltimore, MD)
- …If this is your profile, we want to hear from you. The Associate Director/Director, MSLs is responsible for the leadership, direction and management of MSLs ... their development plans and ongoing performance. Assists other managers ( Associate Directors) with leadership competency criteria including performance management… more
- Aequor (Newbury Park, CA)
- …to manage GRT interactions The responsibilities of the Regulatory Affairs Senior Associate position are: Assist US Regulatory Lead to support regional regulatory ... systems and appropriately archive all regulatory documents and agency communications Review regional component of the Global Regulatory Plan and provide input… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Associate Specialist, Quality Operations Environmental MonitoringSpecific to Environmental and Utility Monitoring, the analyst ... air sampling, surface sampling and non-viable air sampling.Provide data entry, review and approval as required.Provide summaries of test results to appropriate… more
- Merck & Co. (North Wales, PA)
- …Strategy & Commercial Operations (S&CO), to advance standardized content development, and review model solutions.Leading and inspiring with a sense of authority when ... and execute solutions that support the evolution of the US Oncology review board framework. Required Qualifications: Bachelor's degree.Minimum of 5 years of… more
