- Daiichi Sankyo, Inc. (Bernards, NJ)
- …systems, configuration and associated validation activities of Daiichi Sankyo Pharmacovigilance Safety systems, and fulfillment of data change requests. ... and customer experience Querying and ReportsDevelop complex ad hoc safety database searches and report output.For all data... safety database searches and report output.For all data requests, perform self-QC of data to… more
- Merck & Co. (Rahway, NJ)
- …part of the EHS Operational Excellence team, focusing on identifying, collecting, and analyzing data to assess the health of our EHS programs. The role is essential ... and enabling the company to build capabilities better and faster.Key Responsibilities: Data Strategy and Governance:-Lead the development and execution of the EHS… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …calendar, and minutes, and communicate materials, in support of the PSL. Independently evaluates safety data of any source to identify potential safety ... of the Safety Management Plan for assigned product(s)Independently evaluates safety data of any source to identify potential safety signals and… more
- Merck & Co. (Rahway, NJ)
- …The Associate Principal Programmer will write programs to analyze data with statistical methods which are not currently available through commercial software ... Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In... preprocessing, filtering, and manipulation;Programming expertise with clinical endpoint data (efficacy and safety ) and pharmacokinetic … more
- Merck & Co. (North Wales, PA)
- …the benefit of patients and global human health. Our Quantitative Sciences team uses big data to analyze the safety and efficacy claims of our potential medical ... data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the design, development, and delivery… more
- Aequor (Bothell, WA)
- Job Title: Research Associate Contractor Work Location: Bothell, WA 98021 - 100% onsite roleDuration: 6 months contractRequest-ID# 32835-1 Interview Process:Phone ... best candidate and willing to train. Job Description: Seeking a high-performing Associate to join our Manufacturing Science and Technology (MSAT) team in Bothell,… more
- Aequor (Northborough, MA)
- …equipment in strict accordance with SOP's, Good Manufacturing Practices and Safety policies/procedures. Document production activities in batch records, log sheets, ... vials in various stages of packaging completion. Use computer-based systems for data collection, data analysis, timecards, e-mail and inventory management.… more
- Genmab (Plainsboro, NJ)
- …Working Group (LWG) to develop and maintain labeling documents including Company Core Data Sheets (CCDS), Core Safety Information (CSI), United States Package ... to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and… more
- Aequor (Bothell, WA)
- Job Title: Research Associate I Contractor Work Location: Bothell, WA 98021 - 100% onsite role Duration: 12 months contract Request-ID# 32795-1 Interview Process:1st ... (camera on)2nd On-site Job Description:Summary:Seeking a highly motivated and enthusiastic Research Associate II who will be part of the Seattle Pilot Facility (SPF)… more
- Genmab (Plainsboro, NJ)
- …trial and investigator meetings if/as needed Collaboration with Genmab Global Drug Safety :Participate in definition, review, and approval of data packages for ... be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development of… more
- Novo Nordisk Inc. (WA)
- …Drives the understanding and delivery of quality clinical research (patient safety , rights and wellbeing; data reliability; scientific integrity; regulatory ... with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR...and Closure) for assigned sites and clinical trials Verifies safety reporting and the proper handling, monitoring and storage… more
- Tris Pharma (Monmouth Junction, NJ)
- Associate Director/Director, Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. (www.trispharma.com) is ... Junction, NJ headquarters has an immediate need for an experienced Associate Director/Director, Analytical Research & Development. Job Title commensurate with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... data innovation, insights and analytics, delivering patient support solutions, maintaining our facilities and assuring the integrity and completeness of all business… 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 ... and maintenance of animal facilities. This position is responsible for providing data , documentation, and other information as needed for annual reports to Federal… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... data innovation, insights and analytics, delivering patient support solutions,...through the integration of primary market research and secondary data analytics. Incumbent must have the knowledge and technical… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Associate (1st and 2nd shift openings available) as part of the Technical ... according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... all applicable regulations and guidelines and with Company Core Data Sheets and manages deviations. This position interacts across...either the US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages,… more
- Merck & Co. (North Wales, PA)
- …the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of ... multiple stakeholder groups which include clinical development, outcomes research and safety evaluation.The position is a key collaborator with statistics and other… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …DMCs, and Academia. Line management of Senior Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety ... new medicines for patients. The Position This leadership role leads the safety surveillance sub-function within the US East Coast Development Hub comprised of… more
- Merck & Co. (Durham, NC)
- …trenching, mobile crane safety , as well as equipment and machine safety .The ( associate ) specialist will develop a productive working relationship with all ... to audit and provide guidance on how to complete task safely.Education:Required , Associate 's degree in engineering, safety or related technical discipline with… more
