57 compensation analyst jobs found

Merck Job Description The Meeting Guidance and Solutions (MGS) Associate Specialist will be a member of the MGS team that provides consultative services for our end users on our Meeting solutions and conference room systems. They will provide a user first approach to helping our colleagues find the correct solution for their meeting needs and understand the technology and how it works. Primary responsibilities include: Collaborate with business colleagues to understand global, regional, division, and local business requirements to successfully support In person, Hybrid and remote meetings. Collaborating with product and service owners across Information Technology (IT) to identify improvements areas to improve the end user experience. Support our Executive support team with trainings and meeting support for critical executive meetings. Collaborating with product and support teams in the Conference room space to assure that knowledge for our End users is...

Biogen This is a remote position that requires the candidate to be located in the United States. About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components (define.xml and XPTs), and ad hoc analyses. He/She partners with Biostatistics to deliver high quality, submission ready statistical outputs. This person is also responsible for providing input to the Statistical Programming Portfolio Lead (PL) on overall study timelines, monitoring and meeting agreed upon program(s) milestones, escalating issues as needed to their DM counterpart and estimating resources needs. He/She leads a drug program team of statistical programmers to accomplish tasks and communicate issues, as necessary, to senior management....

Biogen About This Role: As a Senior Manager in IT Commercial Data Management, you will play a vital role in enhancing our data capabilities across the organization. Working closely with Enterprise IT and Business Stakeholders, you will lead pivotal initiatives that span Snowflake cloud data engineering, data product ownership, and data quality. This position requires hands-on involvement in daily engineering activities while driving strategic data projects. You will manage data-sharing and analytics as an IT Product Owner, develop innovative data products, and implement data governance across our alliance partnership. Your efforts will directly support our US Analytical teams, offering insights into HCP preferences, engagement, and channel effectiveness, thereby adding significant value to the business. This individual should have the ability to work eastern standard hours. What You'll Do: Serve as IT Product Owner, managing data-sharing and analytics with alliance...

Biogen This is a hybrid position that requires in-person workdays at our facilities in Durham, North Carolina. About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components (define.xml and XPTs), and ad hoc analyses. He/She partners with Biostatistics to deliver high quality, submission ready statistical outputs. This person is also responsible for providing input to the Statistical Programming Portfolio Lead (PL) on overall study timelines, monitoring and meeting agreed upon program(s) milestones, escalating issues as needed to their DM counterpart and estimating resources needs. He/She leads a drug program team of statistical programmers to accomplish tasks and communicate issues, as necessary, to...

Biogen About this role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses. You will partner with Biostatistics to deliver high quality, submission ready statistical outputs with some supervisions. You are responsible for providing input to the Portfolio Lead (PL) on overall study timeline, monitoring and meeting agreed upon study milestones, escalating issues as needed to their PL counterpart and estimating resources needs.You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor. You will represent the Statistical Programming perspective to the study team and is...

Merck Job Description This position is in our organization's Device Development & Technology (DD&T) group in our Research division. Our organization's DD&T group is responsible for the development of devices, combination products, processes, testing and assembly equipment from conception through product launch. Products include autoinjectors, inhalers, implants, infusion pumps, vaginal rings and connected devices/apps. The person in this position contributes to high impact, complex, cross-functional, and cross-divisional teams, initiatives and will provide input to achieve project goals. Effective collaboration with teams is essential to meet our company's goals/objectives. The group also plays a key role in supporting commercially launched products. Our company's DD&T Team is seeking a hands-on medical device product manufacturing and assembly engineer. This position will be responsible for hands-on factory floor work and collaboration, via interfacing...

Merck Job Description PDMB provides data-driven operations and automation support to regulated bioanalytical laboratories. We combine laboratory domain knowledge, robotic work cells, and modern data platforms to ensure reliable, compliant, and continuously improving lab operations. You'll join a multidisciplinary team partnering with lab scientists, automation engineers, IT, Clinical, and QA, to turn operational and scientific data into trusted insights. The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join our LIMS & Data Management group.This role will support work across groups within the Regulated Bioanalytics Department, including work at our Company's new state-of-the-art GxP lab facility in West Point, PA. At this new facility, we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated...

Merck Job Description The Developmental and Reproductive Toxicology (DART) group within Nonclinical Drug Safety (NDS), is seeking a highly motivated person with strong technical skills and diligence to conduct in vivo studies as part of a collaborative team supporting drug development programs. The successful candidate will perform in vivo administration of compound, data collection, cesarean sections with fetal examination, and necropsies under limited supervision. The position requires the ability to maintain neat, concise, and accurate records, along with good oral communication skills. The successful candidate will also train and work cross-functionally, assisting other areas within NDS. This position is for a 5-day work week, including coverage of weekends and Holidays on a rotational basis. Specific responsibilities include but are not limited to: Perform assigned tasks that include dose administration by various routes; recording of body weights, food...

Biogen This role operates on a 2 2 3 schedule for Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations - each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including - Large Scale Cell Culture MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You'll Do Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs) Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation like batch records,...

Biogen Job Description This role operates on a 2 2 3 schedule for Red Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations - each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including - Large Scale Cell Culture MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You'll Do Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs) Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation...

Biogen About This Role The Associate Director, Statistical Programming reporting to Statistical Programming & Clinical Data Sciences Lead, Biogen West Coast Hub. He/She will lead and oversee statistical programming activities of internally and externally through vendors, ensure all statistical programming deliverables in adherence to company SOPs and ICH/GCP. This person leads an indication of a drug program team of statistical programmers to accomplish tasks and communicate issues, as necessary, to senior management. He/She develops and implements standard programming practices while also ensuring that they are employed across a program/Therapeutic Area. What You'll Do * Leads, coordinates and manages timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables of study projects via internal and/or external staff oversight * Provides statistical programming expertise within Biogen, including demonstrated...

Merck Job Description The Cyber Value & Innovation Lead partners with Core Cyber leadership and the Rapid Innovation team to enable informed, valuedriven cybersecurity investment decisions. This role combines strategic thinking, financial rigor, and innovation execution to evaluate emerging cybersecurity capabilities through proofs of concept (POCs), research, and analysis. The role is critical in translating complex cyber and technology initiatives into clear business value while ensuring adherence to financial guardrails and enterprise priorities. Key Responsibilities Innovation Execution & Proofs of Concept Prioritize, lead, and support proofs of concept (POCs) with the Rapid Innovation team to validate emerging cybersecurity capabilities and document results. Strategic Research & Analysis Research cybersecurity trends, threats, and innovation opportunities to shape the POC and investment pipeline. Communicate findings through concise...

Merck Job Description The Cyber Value & Innovation Lead partners with Core Cyber leadership and the Rapid Innovation team to enable informed, valuedriven cybersecurity investment decisions. This role combines strategic thinking, financial rigor, and innovation execution to evaluate emerging cybersecurity capabilities through proofs of concept (POCs), research, and analysis. The role is critical in translating complex cyber and technology initiatives into clear business value while ensuring adherence to financial guardrails and enterprise priorities. Key Responsibilities Innovation Execution & Proofs of Concept Prioritize, lead, and support proofs of concept (POCs) with the Rapid Innovation team to validate emerging cybersecurity capabilities and document results. Strategic Research & Analysis Research cybersecurity trends, threats, and innovation opportunities to shape the POC and investment pipeline. Communicate findings through concise...

Merck Job Description North American GMP Operations, Rahway, NJ We invite individuals who possess a deep passion for promoting lifesaving and life-enhancing products to join our dynamic team. Our team is highly dedicated and committed to offering exceptional scientific oversight, driving the success of our Company's extensive range of products from candidate selection to market authorization. At our company, we proudly continue to build upon a legacy of groundbreaking innovation while steadfastly upholding the highest standards of ethics and integrity. With a workforce representing a multitude of languages and cultures, we stand unified in our collective mission to deliver revolutionary medicines and products with integrity and transparency. We are seeking an enthusiastic Senior Scientist (R3) to join our Rahway, NJ team in Biologics AR&D GMP Operations. The role involves developing and performing analytical methods for raw materials testing, authoring and...

Merck Job Description Associate Principal Scientist, Outcomes Research Under the guidance of a senior leader, the Associate Principal Scientist (Associate Director), Outcomes Research - Head & Neck Cancer will be a member of the overall team responsible for evidence strategy and planning. Will develop and maintain tumor and indication expertise relevant to the asset. Will assess unmet medical need and value across tumors/indications for the asset for asset-level tumor/indication prioritization discussions. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient-reported outcomes assessments, and systematic reviews and meta-analyses. Incumbent is expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product...

Merck Job Description Directors in Quantitative Pharmacology and Pharmacometrics (QP2) apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics, inform dose selection and go/no-go decisions, and shape, present and defend regulatory strategies to support global regulatory submissions and post-approval expansions in indications. Directors perform job duties independently with minimal supervision, lead QP2 efforts on drug development programs, and author strategic documents. Directors are expected to have or be developing expertise in several areas, including: Serving as an expert representative for QP2 on teams developing infectious disease or vaccine assets Framing critical drug development questions for optimizing model-based development Developing and executing translational PK/PD models, population pharmacokinetic models, exposure-response and, stratification biomarker models, quantitative...

Merck Job Description Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to use innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. As an Associate Principal Scientist in the multiscale separations team within the Separations Sciences team of Analytical Enabling Capabilities, you will work within a highly collaborative team to enable the advancement of the development pipeline. You will be primarily responsible for developing analytical and preparative methods for small molecule pharmaceuticals but also peptides, protein-based therapeutics, and emerging modalities. You will work side by side with (bio)process scientists to deploy innovative separation, analysis, and characterization strategies to accelerate the development of new medicines and vaccines. To accelerate the...

Merck Job Description Directors in Quantitative Pharmacology and Pharmacometrics (QP2) apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics, inform dose selection and go/no-go decisions, and shape, present and defend regulatory strategies to support global regulatory submissions and post-approval expansions in indications. Directors perform job duties independently with minimal supervision, lead QP2 efforts on drug development programs, and author strategic documents. Directors are expected to have or be developing expertise in several areas, including: Serving as an expert representative for QP2 on teams developing infectious disease or vaccine assets Framing critical drug development questions for optimizing model-based development Developing and executing translational PK/PD models, population pharmacokinetic models, exposure-response and, stratification biomarker models, quantitative...

Merck Job Description The Molecular & Viral Safety group within Cell-Based Sciences is seeking a detail-oriented, technically skilled Senior Scientist to support daily operations in our Next Generation Sequencing (NGS) laboratory and contribute to multidisciplinary analytics. This hands-on role is ideal for someone with a strong background in molecular biology techniques and an interest in basic bioinformatics and computational workflows. The successful candidate will be responsible for executing established protocols for nucleic acid extraction, library preparation, sequencing, and will perform routine data processing and basic bioinformatics analyses. The senior scientist will collaborate within a dynamic, integrated, and multidisciplinary team supporting both vaccine and biologics modalities and will contribute to the development and implementation of nextgeneration sequencing technologies to help ensure that our products are free of adventitious agents as well as...

Merck Job Description Summary of Position: Our Company's Industrial Hygiene Laboratory (IHL) group within the Safety Center of Excellence (COE) is seeking a highly motivated individual for an Associate Chemist position. The Associate Chemist will be responsible for performing routine industrial hygiene (IH) sample analysis using LC/UPLC, MS, and ELISA techniques. Using precise analytical skills and understanding of chemical principles, the successful candidate will perform analysis of air and surface samples for a variety of active pharmaceutical ingredients (APIs) both small and large molecules using approved analytical methods. Must have the ability to work independently using laboratory instrumentation and computer systems. The successful candidate will maintain accurate records and comply with laboratory operation and safety SOPs. Working within the requirements of ISO 17025 is expected. The IHL Associate Chemist will demonstrate analytical proficiency on a...