Regulatory Affairs Quality Associate

Job DescriptionThe Sr. Manager, Regulatory Affairs plays a crucial role in integrating and applying knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of TK-CHAIN LLC's drug development programs, policies, and procedures; ensuring a compliant state of regulatory commitment.This position...

Gardner Resources Consulting, LLC is seeking a skilled Pharmaceutical Regulatory Affairs Expert to join our team. As a regulatory affairs expert, you will play a key role in ensuring compliance with US pharmaceutical industry and healthcare landscape guidelines.Estimated Salary: $120,000 per yearAbout the Job:This position requires a thorough understanding...

Job Description:At TK-CHAIN LLC, we are seeking a highly skilled Regulatory Operations Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for overseeing and managing the assembly and publishing of all documents while maintaining adherence to FDA standards and internal requirements.Responsibilities:Coordinate...

Job Summary:">This position is responsible for overseeing the assembly and publishing of regulatory documents, ensuring adherence to FDA standards and internal requirements. The ideal candidate will have excellent communication skills, in-depth knowledge of FDA guidelines, and a strong critical thinking ability.">About TK-CHAIN LLC:">TK-CHAIN LLC is a...

Bristol Myers Squibb is a leading biopharmaceutical company committed to transforming patients' lives through science. We are seeking an experienced Senior Counsel, Regulatory Law to join our team.As a Senior Counsel, you will play a critical role in providing legal support to various stakeholders within Global Medical, Global Commercialization Excellence,...

Job OverviewWe are seeking a highly skilled Associate Director, Medical Affairs to join our team at UroGen.Key Responsibilities:Support Medical Affairs Strategy: Collaborate with internal and external stakeholders to develop and execute medical communications plans aligned with the company's objectives.Operational Support: Provide strategic and operational...

About the RoleGenmab A/S is seeking an experienced Director, Legal Counsel to join its existing Legal team in Princeton, NJ. This is a critical role that will provide a robust, full-service legal function supporting Genmab's US Market Operations organization.Key ResponsibilitiesProvide legal review of scientific and commercial/marketing materials for use in...

About the RoleClinical Trial Liaison Manager at BESTMSLsOverviewThis Hybrid office-based position involves regular travel in the field, overseeing site trial delivery, subject recruitment, protocol adherence, and data quality. Based in North America, you will represent the company in site relations, support study teams with startup and recruitment, and...

ResponsibilitiesDevelop and implement a regulatory document strategy to support our clinical development programsCreate high-quality clinical documents, including protocols, clinical study reports, and investigator brochuresCollaborate with cross-functional teams to ensure document accuracy and complianceManage competing priorities and deadlines to deliver...

About Aequor TechnologiesWe are a leading provider of innovative solutions in the pharmaceutical industry. Our mission is to deliver high-quality products and services that meet the evolving needs of our customers.Job SummaryWe are seeking an experienced Clinical Quality Assurance Associate to join our team. As a Clinical Quality Assurance Associate, you...

Job Title: Clinical Trial Liaison ManagerThe Clinical Trial Liaison Manager is a key position at BESTMSLs, responsible for overseeing site trial delivery, subject recruitment, protocol adherence, and data quality. This hybrid office-based role requires regular travel in the field.Responsibilities:Site and Investigator Relationship ManagementRepresent the...

About UsBESTMSLs is a leading company in the clinical trial industry, dedicated to providing exceptional services and expertise to our clients.Job DescriptionWe are seeking an experienced Clinical Trial Liaison Manager to join our team. The successful candidate will be responsible for overseeing site trial delivery, subject recruitment, protocol adherence,...

Genmab is seeking a seasoned Medical Education Leadership and Strategy Director to lead the development and execution of its independent medical education grants strategy and operations across therapeutic areas.The ideal candidate will serve as the lead for initial review of all corporate funding requests, ensuring close oversight and coordination of GMA...

We are seeking a highly skilled Senior Quality Assurance Engineer to join our team at Diversity Nexus.About the RoleIn this key position, you will be responsible for overseeing the quality assurance of software development processes in the pharmaceutical industry. Your expertise will ensure that our products meet global regulatory requirements and exceed...

Job TitleClinical Supply Management Expert - PMV PharmaOverviewPmvpharma is a company that requires expertise in clinical supply management. The ideal candidate will have experience in planning, forecasting, and managing clinical supplies.Estimated Salary Range:$120,000 - $180,000 per year, based on the location of the position and the candidate's level of...

About the RoleThe Bristol-Myers Squibb Company seeks a Senior Manager to join its World Wide Medical Neuropsychiatry Strategy team. This is a unique opportunity to partner with key medical teams to support the development and implementation of disease area and asset-specific medical strategies.This role will involve collaborating with cross-functional teams,...

**Overview**We are seeking a highly organized and detail-oriented Administrative Support Specialist to join our team in providing administrative support to the Vice President, Global Quality, and the Global Vice President of Regulatory.**Responsibilities:**Manage complex calendars, coordinating internal and external meetings as neededCoordinate travel...

As a key member of our team, you will oversee quality inspection activities across various automotive manufacturing facilities within a two-hour radius of Princeton, Indiana. This role involves extensive travel and may require overnight stays.Job OverviewEnsure that automotive manufacturing processes adhere to quality standards and specifications....

As a key member of our team, you will be responsible for providing high-quality cleaning services to our clients. With a strong focus on customer satisfaction, we are seeking a reliable and detail-oriented individual to join our team as a Hospitality Services Associate.About the RoleThis is a full-time position that involves performing various cleaning...

**Company Overview**Dow Jones, a leading provider of business and financial information, is seeking an experienced Research Editor to join our Due Diligence team. As a Research Editor, you will play a crucial role in the creation of high-quality reports on companies and/or individuals using a combination of publicly-available sources and proprietary...