Amgen Jobs in Arkansas

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This is a leadership position within Amgen’s Process & Product Development organization. This Principal Scientist will be responsible for leading a group of scientists that develop early and late phase recovery and purification processes for Amgen’s large molecule pipeline. Responsibilities include purification process development that utilizes harvest, clarification, chromatography, and/or filtra...
Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidne...
To support the regulatory, safety and product development needs of the Amgen Biosimilars Operating Unit through detailed development and implementation of global regulatory strategies, submissions, and plans. - Coordination of global regulatory CMC activities relevant to the successful execution and implementation of biosimilar CMC regulatory strategies and plans - Development of CMC and analytica...
The position's primary responsibilities may include oversight of the development and qualification of analytical methods for proteins and leading state-of-the-art characterization of protein therapeutic candidates. Other responsibilities include communicating project updates as appropriate, and generation of regulatory submissions, publications or patents. The candidate will actively chart the cou...
Amgen is investing in creating a new start-to-finish drug product facility. This facility will encompass operations from UF/DF to fill/finish and house high, throughput, state-of-the art analytical technologies to add new capability and higher capacity to perform drug product development. This Principal Scientist position is to lead the technical operations in the drug product workstation, part of...
The purpose of this group is to provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formulate and communicate the regulatory promotional position for approved products Key A...
This position can be located at either of our Thousand Oaks, CA or Rockville, MD locations. The Senior Manager will provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formu...
Amgen, Thousand Oaks, CA is seeking a highly motivated and team-oriented candidate for the position of Senior Scientist in the Biosimilar Business Unit Process Development group in Analytical Sciences. The Senior Scientist will support the development of several biosimilar projects including the planning and execution of analytical similarity strategy. The individual will effectively interface wit...
The Director, Global Study Management (GSM) sits within our Global Development Organization which, through operational excellence in clinical trials works to deliver high-quality clinical evidence to advance our pipeline and comply with requirements of relevant bodies. The Role Deliverables: •Serve as the primary point of contact for clinical trial execution for allocated studies within the Genera...
The HEALTH POLICY & REIMBURSEMENT SENIOR MANAGER will support the US Health Policy & Reimbursement team’s leads for Federal (US) payer issues across one or more Therapeutic Areas, Federal Agency Engagement, or Health Policy areas by (1) representing Federal (US) payer needs, (2) communicating about the payer planning process, and (3) and managing assigned aspects of the Federal (US) payer engageme...
This position is responsible for conducting internal compliance investigations globally within Amgen’s Worldwide Compliance & Business Ethics function. This includes: • Preparing written investigation plans; • Reviewing relevant documents and evidence; • Conducting witness interviews; • Analyzing facts and reaching conclusions as to whether or not compliance violations occurred and, if so, conduct...
This position is a field-based position for the Oncology therapeutic area Regional Medical Liaison (RML) group within the Scientific Affairs organization. The territories cover Long Island, NY. The Senior Regional Medical Liaison (Sr RML) will interact with Oncology Healthcare Decision Makers to communicate and advance the scientific platform as aligned with Amgen's corporate goals and objectives....
The Biostatistics Manager is responsible for: • Ensuring all statistical aspects of documentation pertaining to clinical activities meet required standards and are statistically correct • Influencing study design, and defending statistical approaches internally and externally • Leading one complex or multiple less complex studies/projects • Adhering to all Amgen Policies, SOPs and other controlled...
The GCP Compliance Strategy Lead is a global role based in Thousand Oaks, US. The GCP Compliance Strategy Lead reports to the GCP Compliance Strategy Director in Global R&D Compliance and Audit (GRDCA); The role of the GCP Compliance Strategy Lead is to provide proactive GCP compliance oversight and guidance to assigned functional areas and stakeholder groups within the R&D organization. This incl...
Amgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. With a deep and broad pipeline of potential new medicines, we continue to advance science to serve patients. Serves as point of contact for regulato...
We are currently seeking Economic Modelers to join the Global Economic Modeling Center. We work in international cross-functional teams developing and supporting product value strategy focusing on evidence-based economic modeling throughout product life-cycle. The activities involve early modeling for strategic input to development design and pricing, core models for use as basis for local model a...
This role - based at Amgen's Thousand Oaks, California headquarters - will be in the Bone and Neuroscience Therapeutic Area, focusing on romosozumab (AMG 785), and will be responsible for: - Coordinating input for design of clinical trials within a program; identifying and resolving cross-regional issues impacting study design - Assuming primary ownership and authorship for study concept documents...
The Biostatistical Programming Manager will work in Amgen's Medical Sciences Biostatistics (MSB) organization and will be based at Amgen's headquarters in Thousand Oaks, California. Responsibilities include: • Function as study lead programmer for multiple Early Development clinical trials: o set up the study-level programming environment o project-manage programming activities on the study, ensur...
The Biostatistical Programming Manager will work in Amgen's Global Statistical Programming (GSP) organization in one of the six therapeutic areas and can be based at Amgen's headquarters in Thousand Oaks, California or at Amgen's South San Francisco or Seattle, Washington locations. Responsibilities include: • Function as study lead programmer on one or more Phase 2 and 3 clinical trials: o set up...
The call center analyst is responsible for the generation of key indicator reporting, creation of reporting dashboards, and analysis of volume flow, productivity, and quality performance to manage the performance of our access and reimbursement suppliers and to drive continuous improvement, efficiency, and automation initiatives. The call center analyst is also responsible for the creation and mai...
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