Global Regulatory Lead, Oncology

Responsibilities: Develop global regulatory strategy for Oncology products in development and through life cycle management considering all relevant guidance, commercial needs, and company objectives. Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance,...

Purpose Ensure the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic portfolio. This goal must be achieved both as a component of an overall global regulatory approach and ensure compliance with both...

About the Department Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D community based on collaboration,...

Unlock Your Potential as a Traveling Oncology RNWe're seeking a skilled Oncology Registered Nurse to join our team of travel healthcare professionals. As a Travel RN with Lead Healthstaff, you'll have the opportunity to make a positive impact on patient care while enjoying a high-paying and flexible lifestyle.Key Benefits:Competitive weekly payComprehensive...

Unlock Your Potential as a Travel Oncology RNWe're seeking a skilled Oncology Travel Registered Nurse to make a meaningful impact on patient care. At Lead Health, we're dedicated to providing exceptional opportunities for healthcare professionals like you.Key Highlights:12-hour night shifts, 36 hours per week13-week assignment at a reputable healthcare...

Adecco is seeking a skilled Senior Regulatory and Compliance Specialist to support global regulatory compliance within the pharmaceutical industry. The ideal candidate will be experienced in pharmaceutical regulations, compliance practices, and their impact on manufacturing. This role offers high visibility, working across various functional areas including...

Our client is looking to conduct interviews the week of 9/23. Applicants must be available to start ASAP as well as comfortable working fully onsite Mon-Fri in Lawrence Township NJ. This is a contract role that will last through the end of the year, there are potential extensions. The role is open due to increased end of year volume. Title: Benefits Program...

Overview About Berry Harnessing the strength in our diversity and industry-leading talent of 40,000+ employees across more than 250 global locations, we develop, design, and manufacture innovative products with an eye toward the circular economy. At Berry Global, we believe in the extraordinary power of people and their unique talents, experiences,...

{"Responsibilities": "Key ResponsibilitiesMaintain NCMR systemMaintain calibration systemRespond to customer requests and complaints as necessaryCoordinate special projects for the QA department as necessaryEnsure accuracy of Quality recordsMaintain microbiological testingProvide training needs of QA employeesPerform annual Gauge R&R studiesMaintain quality...

Job SummaryBristol Myers Squibb is seeking a highly skilled Associate Director, Drug Development Project Management to join our team. As a key member of our Global Program Team, you will be responsible for leading the strategic and operational planning and decision-making process for early and/or late development programs.Key ResponsibilitiesPartner with the...

Duration: 4 month contract (potential extensions) Location: Titusville, NJ (1x per week on site) Required Skills & Experience10+ years' in project management or consulting with recent focus in data science and/or advanced analytics 5+ years' in Commercial Pharmaceutical industry Knowledge of AI/ML Modeling, Data Engineering, and Analytics technical concepts...

About the RoleWe are seeking an experienced Associate Director, Drug Development Project Management to join our team at Bristol Myers Squibb. As a key member of our Global Program Team, you will be responsible for leading the strategic and operational planning and decision-making process for early and late development programs.Key ResponsibilitiesPartner...

Job Description: Role is 50% onsite CW can work from Giralda Farms, NJ. or Lawrenceville, NJ Position Summary: The Clinical Trial Disclosure Senior Specialist will provide the operational support of: - Redaction of clinical trial documents in accordance with evolving global regulations. Key business partners are Clinical Development/Early Development Leads,...

Job DescriptionAs the Head of Global Facilities Engineering at Biogen, you will be responsible for leading the strategic technical direction for facility assets, ensuring alignment with industry standards and operational excellence. This role will report into the VP of Global Engineering and Facilities and will champion subject matter expertise across...

Job SummaryThe International Regulatory Compliance Specialist is a critical role within J&J Snack Foods, responsible for ensuring the company's products comply with international regulations and customer requirements. This position requires a deep understanding of federal, local, state, and international food laws and regulations.Key ResponsibilitiesVerify...

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap –...

Job#: 2047252 Job Description: Senior Scientist II, Oncology 2047252Location: Lawrence, KS (Onsite) Science/ Focus: OncologyJob Overview: We are looking for a motivated Senior Scientist with expertise in biology and drug discovery to develop new cancer treatments as part of our clients collaborative oncology research team.Primary Job Responsibilities:Design...

About the RoleBristol Myers Squibb is seeking a highly skilled and experienced Clinical Trial Physician to join our team in Rheumatology. As a key member of our Clinical Development organization, you will play a critical role in the design, execution, and interpretation of clinical trials.Key ResponsibilitiesProvide medical accountability and oversight for...

Job DescriptionDeciphera Pharmaceuticals, a member of ONO, is a biopharmaceutical company dedicated to discovering, developing, and commercializing innovative medicines to improve the lives of people with cancer. Our proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology enable us to develop a diverse portfolio of...

Job Title: Benefits Program Lead/ManagerOur client, a leading company in the industry, is seeking a highly skilled Benefits Program Lead/Manager to join their team.Job Summary:The Benefits Program Lead/Manager will be responsible for ensuring the smooth administration of benefits programs, including health and welfare and retirement plans. This includes...