- Merck & Co. (Rahway, NJ)
- …set up)Lead medical monitoring team in review and interpretation of clinical data /medical protocol-deviations in collaboration with the Clinical ... Job DescriptionPosition Description: Associate Director, Clinical Scientist This position...Program Lead, you will collaborate with global, cross -functional team members including clinical directors and study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit ... Authorization Applications (MAAs), and local country submissions. Collaborates with PSL/ Clinical Safety Physician(s) and cross-functional team to develop… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …a difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific ... (subset of) NACD and/or as part of a global team and as aligned to a business case, goals...relevant regulatory requirements Ensure accuracy, validity and completeness of data collected at clinical trial sites in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with… more
- Merck & Co. (Rahway, NJ)
- … clinical data repository from external biomarker vendors. Work with Clinical team and/or Central labs to design sample collection kits, laboratory ... candidate will work closely with Biomarker leads, Assay scientists, Vendor Managers and Clinical team to ensure that critical timelines are meet by our… more
- Merck & Co. (Rahway, NJ)
- …and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the ... The Associate Principal Programmer will write programs to analyze data with statistical methods which are not currently available through commercial software… more
- Merck & Co. (North Wales, PA)
- …and high-quality data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the ... of patients and global human health. Our Quantitative Sciences team uses big data to analyze the...Specific Required Skills and Experience:Significant expertise in SAS and clinical trial programming including data steps, procedures,… 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 ... and posters/oral presentations that report results from our company's General Medicine clinical trial program, as well as select early-stage development projects and… more
- Merck & Co. (North Wales, PA)
- …support for related drug/vaccine projects in Late Development Statistics.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and other ... and ascertains needs for potential program development of novel statistical methodology.Analyzes data and interprets results from clinical trials to meet… more
- Merck & Co. (Rahway, NJ)
- …validation of Mass Spectrometry based assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position ... is seeking a highly motivated candidate to join our team . The individual will play a critical role in...clinical trials.Writing memos, final reports and publications summarizing data , and writing/updating lab SOPs.Serve as a subject matter… more
- Merck & Co. (North Wales, PA)
- …other team members when opportunities arise.Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO,… more
- Merck & Co. (Rahway, NJ)
- …BS degree in relevant discipline.-Knowledge and Skills:--Minimum 6 years' experience in Clinical Data Management or Pharmacovigilance as appropriate to business ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs,… more
- Merck & Co. (Rahway, NJ)
- …company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes for diverse ... biotherapeutics, and efficiently manufacture material to supply clinical trials. We are also responsible for commercial process development and the development and… more
- Merck & Co. (North Wales, PA)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck & Co. (Boston, MA)
- …Description We are seeking an experienced and skilled Cheminformatician and AI/ML data scientist to join the Cheminformatics group within Modeling and Informatics ... ability to translate scientific needs into actionable plans for implementing data workflows and infrastructure that accelerate the decision-making process from hit… more
- Aequor (New York, NY)
- …approaches and tools in health services research is required, eg, literature review, clinical data interpretation and claim data analysis Knowledge of ... Job Description: This is a full-time 12-month consultant/research associate (RA) position in 's Pneumococcal Vaccine Global...'s Pneumococcal Vaccine Global Access Strategy and Pricing (GASP) Team . The candidate for this role will support ongoing… more
- Merck & Co. (Boston, MA)
- …worldwide depends on the integrity, creativity, humility and scientific acumen of our team .-We are creating a diverse organization that is inspired by invention and ... Bioanalytics (PDMB) group is seeking a dynamic, strategic thinking and collaborative Associate Principal Scientist to contribute to our small molecule and peptide… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …global sites. These business functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, ... and reuse. Maintains detailed Solution Architecture diagrams for ALL systems, integrations, and data flows. Work with the Enterprise Architecture team to ensure… more
- Aequor (Thousand Oaks, CA)
- …experience. Candidates should have some experience with contracts. Technical platforms the team uses: SAP, Ariba, C3, salesforce Role 1: More transactional - ... receiving contracts - data entry to c3 compliance system using templates, generating...business challenges with outstanding people, tools, and processes. The team delivers on key initiatives and capabilities to support… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Associate as part of the Technical Operations team based in Raritan, ... all applicable regulations.Key Responsibilities Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical… more
