R & D Jobs in Thousand Oaks, California

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49 Thousand Oaks, CA R & D jobs found on Monster.

Jobs 1 to 20 of 49
Company: Yoh HTA Submissions Specialist needed for a contract opportunity with Yoh's client located in Thousand Oaks, CA. Top Skills You Should Possess: - HTA / reimbursement submissions - Pharmaceutical industry experience - Dossier development What You'll Be Doing: - Provide writing support to prepare the required clinical and economic sections of a country specific HTA / reimbursement su...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Chief Scientific Officer Thousand Oaks, CA Full-Time $100,000 - $160,000 Apply Apply Chief Scientific Officer Thousand Oaks, CA Full-Time $100,000 - $160,000 Apply Job Details If you are a Chief Scientific Officer, Software product with experience, please read on! We are leader in our industry,...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 37 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized laborator...
Amgen is seeking an experienced professional to work in a client-facing Senior Manager Position within the Scientific Affairs (SA) organization of R&D, specifically on the Intercontinental (IC) and Medical Development Teams (MDT). The position will report directly to the IC SA Director with a dotted line to the IC Executive Medical Director. The successful candidate will provide cross-functional ...
The US Medical Organization Medical Director supports the implementation of US Medical strategies, including US launch and lifecycle management. *The Medical Director is responsible for: -Supporting the development, execution and communication of the US Medical Team (USMT) plan -Supporting the US Medical Leader in the launch planning process to ensure alignment between medical and brand activit...
The Senior Manager works in Amgen's broader Global Regulatory Affairs and Safety (GRAAS) organization and leads the RAGLO team in support of regulatory filings and implementation requirements for packaged PCL and RPI components. The RAGLO Senior Manager, under the supervision of the corporate Global Labeling Department Head, manages and facilitates the creation/update of commercial artwork that i...
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. Group Purpose: The Device Regulatory ...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 36 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
The Clinical Research Medical Director (Biosimilars) is responsible for: * Supporting the development, execution and communication of the global clinical plan * Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program * Participating and providing clinical input into safety and regulatory interactions * Supp...
Associate Project Manager - Pharmaceutical Job Description: Basic Qualifications • Administrative experience in life sciences or medically related field • Clinical trials process experience • Work involving data entry into systems/databases and/or business support role Minimum requirements: Preferred Qualifications • BA/BS/BSc in the life sciences • Work experience in life sciences or med...
Contract Sr. Clinical Project Manager The Sr Project Manager provides project management support and leadership to the E2E SC workstreams, sub-workstreams and teams, and is accountable to the PMO lead his/her workstream lead/s. The Sr Project Manager must apply project management best practices in the development, initiation, planning, execution, control and closing of workstream projects, accord...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply CLS Supervisor West Hills, CA Full-Time $95,000 - $100,000 Apply Apply CLS Supervisor West Hills, CA Full-Time $95,000 - $100,000 Apply Job Details Clinical Laboratory Scientist Supervisor If you are a Clinical Laboratory looking to join a great organization, please read on! Our client is a le...
Company: Yoh Senior Associate Research Operations needed for a contract opportunity with Yoh's client located in Thousand Oaks, CA. Top Skills You Should Possess: - HPLC - analytical What You'll Be Doing: - This position will provide formulation support for commercialization of protein therapeutics. - formulation/analytical support for drug product process characterization, commercial SKU d...
Market Research Manager - Contract/Temp, Pharma/Biotech A growing biopharmaceutical company located in the Ventura County area is seeking an experienced Market Research / Market Planning Manager to join the Market Research team. The qualified Market Research / Market Planning Manager candidate will be responsible for managing primary and secondary market research analysis and providing analytical...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 37 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Consider joining Eurofins at Lancaster Laboratories where people are the most important element in our chemistry. With over $1 billion in annual revenues and 15,000 employees across 190 sites in 36 countries, Eurofins Scientific is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer pr...
Global Regulatory Affairs (GRA) provides global regulatory leadership, expertise, and execution for the development, registration, and lifecycle management of all Amgen molecules. This role is a product facing role that leads the Global Regulatory Team (GRT) in the Regulatory Affairs organization. The purpose of this role is: * To lead one or more GRTs within Amgen’s GRA department * To develop...
Biosimilars are important development products for Amgen and for patients globally. The opportunity to provide patients with greater access to critical therapies furthers the Amgen mission to serve patients. To facilitate efficient global registration of the Amgen biosimilar portfolio, the Biosimilars Regulatory Affairs Manager, Rest of World (ROW), will be responsible for ensuring that specific c...
This role is the lead of a regional Regulatory Affairs organization within an assigned area. The purpose of this role is: * To provide management and leadership by advising on the development and execution of regulatory strategy and plans for regulatory agency interactions * To ensure appropriate regulatory input is provided into regulatory plans * To provide oversight of Regional Regulatory Le...

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