better Project Program Mgmt Job at Biotechnology Pharmaceuticals

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

Program Director Job Type: Full-Time Location: Cambridge, MA Job Description: Job Description - Program Director Program Directors oversee projects within technology platforms or franchise indications, and are key leadership positions within Alkermes, Inc. Program Directors work with senior leaders to establish the overall strategy and key milestones for development projects. Program Directors establish and lead development teams in all aspects of product development from early phase through commercialization

Job Description: At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical

Director/Sr. Director, Program Management Core Team Leader, Large Molecule Programs The Product Development function is seeking a seasoned professional to lead our genetic disease programs, several of which are currently marketed products. The individual will have primary responsibility for leading all lifecycle aspects including business, science and commercial development activities. This individual will be the key contact and have responsibility for interfacing with internal constituents, external

Project Manager/Sr. Project Manager, Phase II-IV Req. Code : PMIIIV508 Location : 1. Wilmington NC US 28405 2. Morrisville NC US 27560 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Project Management, Clinical Research Job Description : AAIPharma, is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies

Project Manager/Sr. Project Manager, Phase II-IV Req. Code : Rgpm508 Location : Wilmington NC US 28405 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Project Management, Clinical Research, Regionally-Based Positions Job Description : AAIPharma, is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies to

Associate Project Manager Req. Code : APM1008 Location : Wilmington NC US 28405 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Biotechnology and Pharmaceutical, Project Management, Clinical Research Job Description : AAIPharma is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies to meet exciting drug

Project Manager Req. Code : Pmphase1 Location : Morrisville NC US 27560 Travel Required : None Job Type : Full Time Career Level : Experienced (Non-Manager) Education : Bachelor's Degree Category : Project Management, Clinical Research Job Description : AAIPharma is a leading international provider of pharmaceutical and biotechnology product development services. Our employees work in state-of-the-art facilities using leading edge technologies to meet exciting drug development challenges. We are seeking candidates

DescriptionCordis, a member of Johnson & Johnson's Family of Companies, is recruiting for a Lead Project Management Associate, located in Menlo Park, CA. Ground breaking, life changing careers that reward the power of ideas and innovation. For more than 40 years, Cordis Corporation has pioneered less invasive treatments for vascular disease. Technological innovation and a deep understanding of the medical marketplace and the needs of patients have made Cordis the world's leading developer and manufacturer

Process Operator II AutoReqId 6305BR Job Description Under close supervision, performs a variety of processing duties according to batch record and Standard Operating Procedures (SOPs) in Small Scale Manufacturing including, but not limited to, weighing, mixing, fabricating, coating, and pouching/packaging. Essential functions include: .Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. . Reports process or equipment problems to supervisor

Job Title Mgr, Project II AutoReqId 6070BR Job Description Under general guidance from Engineering Operations Manager, responsible for leading, coordinating and managing Packaging Equipment and process/systems projects including analysis, design and implementation. . Performs Project Management and project implementation functions including the preparation of scope documents, risk analysis, cost justifications, validation protocols, capability studies, engineering tests, project schedules, project budgets, project

Job Title Mgr, Project II AutoReqId 5733BR Job Description Under general guidance from Engineering Operations Director, responsible for leading, coordinating and managing facility, equipment and process/systems projects (e.g. facility expansion or redesign, new equipment or systems) including analysis, design and implementation. Oversees and manages major improvement studies. Oversees and manages all functions relating to the planning, design and implementation of facility, equipment and process/system projects

Process Operator III AutoReqId 5897BR Job Description Under limited supervision, performs a variety of processing duties according to batch record and Standard Operating Procedures (SOP's) in the manufacturing department including, but not limited to, cleaning, weighing, mixing, fabricating, coating, pouching, cartoning, packaging, and operating a minimum of various manufacturing equipment including the processes surrounding the equipment. This is an advanced journey-level position in the Process Operator class

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

At Wyeth, we have a vision of leading the way to a healthier world. We've committed ourselves to achieving this vision by making quality, integrity and excellence the hallmarks of our business. A Fortune 500 company and global leader in pharmaceuticals, consumer healthcare, and animal healthcare products, we know that our employees are who keep us on the cutting edge of innovative discoveries and superior customer service. To sustain and enhance our leadership position in the pharmaceutical industry, we continue

Shape Your Future And Ours. Schering-Plough is an innovation-driven, science-centered global health care company. Through our own biopharmaceutical research and collaborations with partners, we create therapies that help save and improve lives around the world. We apply our research-and-development platform to human prescription and consumer products as well as to animal health products. Schering-Plough's vision is to 'Earn Trust, Every Day' with the doctors, patients, customers and other stakeholders

Program Manager, Standards Acquisition (WP) Job Type: Full-Time Location: Rockville, MD Job Description: Function of the Position: The Program Manager position is responsible for input to and output of information related to the start of the USP standards-setting process in monographs and reference standards. The position will be given responsibility for USP's new donor recognition program, which aims to keep donors to USP's programs well informed of the status of their donations, and adequately recognized

Shape Your Future And Ours. Schering-Plough is an innovation-driven, science-centered global health care company. Through our own biopharmaceutical research and collaborations with partners, we create therapies that help save and improve lives around the world. We apply our research-and-development platform to human prescription and consumer products as well as to animal health products. Schering-Plough's vision is to "Earn Trust, Every Day" with the doctors, patients, customers and other stakeholders

Auto req ID 387BR Position title external Project Manager, SMP Department Sales Operations Location Marlborough, MA - Headquarters Job type Full-time Summary of Responsibilities SUMMARY OF KEY RESPONSIBILITIES 1. Assist with managing the SMP calendar and scheduling of Sales, Training and Home Office programs to minimize conflicts and maximize scheduling efficiencies 2. Produce and coordinate the marketing and communication of all SMP managed programs to maximize attendance to ensure cost efficiencies are achieved

Novartis Institutes for BioMedical Research is Novartis' global research organization and is committed to discovering innovative medicines that cure disease and improve human health. By conducting more relevant and predictable drug discovery that can yield new and better medicines for patients, Novartis Institutes for BioMedical Research is redefining drug discovery in the post-genomic era. Over the past four years, Novartis Pharmaceuticals has had the greatest number of new molecular entities approved by

Merck & Co. Inc., established in 1891, is a global research-driven pharmaceutical company dedicated to putting patients first. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences and a resounding passion for improving human health. As part of our global team, youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. The Project Manager will support the analytical and decision support

Our passion for patient-focused healthcare technology begins with our focus on you. Partner with McKesson Pharmaceutical and you'll partner with a company that is making a real difference in medication supply management. We're empowering healthcare by reducing inefficiencies and waste, and positively impacting patient care. And we believe the best way to deliver patient-focused care is to care about you. That's why we're passionate about supporting your desire to drive the pharmaceutical solutions of the future

Novartis Institutes for BioMedical Research is Novartis' global research organization and is committed to discovering innovative medicines that cure disease and improve human health. By conducting more relevant and predictable drug discovery that can yield new and better medicines for patients, Novartis Institutes for BioMedical Research is redefining drug discovery in the post-genomic era. Over the past four years, Novartis Pharmaceuticals has had the greatest number of new molecular entities approved by

Description Cordis, a member of Johnson && Johnson's Family of Companies, is recruiting for a Lead Project Management Associate, located in Menlo Park, CA. Ground breaking, life changing careers that reward the power of ideas and innovation. For more than 40 years, Cordis Corporation has pioneered less invasive treatments for vascular disease. Technological innovation and a deep understanding of the medical marketplace and the needs of patients have made Cordis the world's leading developer and manufacturer

Position Title Protocol Project Manager Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description Protocol Project Managers are responsible for identifying and managing the supply chain responsible for satisfying the protocol specific clinical supply demand. The Protocol Project Manager is responsible for interacting with their Clinical partner to best define the drug demand profile forecasted for the subsequent 18-month period. The Protocol Project Manager will ensure that

Position Title Master Planner Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description Summary of Position Support the clinical supply chain within SPRI. The position is charged with assuring that all clinical supply operations facilities/groups are appropriately loaded (based on pre-defined business rules) with workload and there is full transparency to all forecasted workload. Furthermore, the position maintains workload business rules for all clinical supply operations

Position Title Program Project Manager Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description Program Project Managers are responsible for identifying the global demand profile and requirements for Clinical Trial Studies. These studies are planned and initiated by Clinical Development, Global Medical Affairs, US Marketing, Country Operations, SPKK and Toxicology functions (herewith to be called the ‘Customers’). The Project Manager is responsible for communications

Position Title Distribution Project Manager Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description Summary of Position The position is charged with providing distribution-related project management support to Global Clinical Supply Planning (GCSP) Leadership and GCSP Project Managers. This will include training, maintenance and enhancement of distribution planning tools, as well as providing protocol-specific planning support and offering creative solutions to distribution

Position Title Project Leader, Clinical Programming Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description Serve as a project lead for SAS® programming activities supporting Phase I-III clinical trials. Responsibilities include developing reporting databases and derived analysis datasets and providing outputs for the Clinical Study Report, the Clinical Summary of Safety and electronic files for submission to FDA and global regulatory agencies. Oversee programming activities

Position Title Clinical Project Manager - Respiratory / Allergy Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description The Clinical Project Manager (CPM) inGlobal Clinical Trial Management (GCTM)will function as a Study Team Leader by organizing and managing all operational aspects of the study from conception to submission while ensuring adherence to timelines. The CPM will also proactively address risk management through contingency planning. The CPM will manage critical

Position Title Director, Global Programs and Services Business Division Global Functions - Human Resources Country U.S.A. Location NJ Union Job Description This position leads the efforts of a team of project/program managers in the design, development and implementation of global programs, processes and tools to support the functions of Global Staffing and Diversity & Inclusion. In addition, this position will work to leverage the programs of each of the individual functions across the others. This individual

Position Title Project Manager -Clinical Trial Registry - Medical Communications Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description This position is responsible for project management and compliance activities within Medical Communications. · Provide project management support for Clinical Trial Registry and Results Disclosure. · Manage document timelines and Med Comm project plans for clinical development program documents and submissions. ·

Position Title Business Planner, Corporate Accounts/Specialty Business Division Global Pharmaceutical Business Country U.S.A. Location NJ Kenilworth Job Description The Business Planner, Corporate Accounts/Specialty is responsible for reporting, analysis, business planning and development along with various administrative operations for the Corporate Accounts and Specialty Teams of the USMM Organization. This includes, but is not limited to, the conception and development of key performance indicators, strategic

Position Title Category Project & Planning Manager Business Division Global Specialty Operations - Consumer Healthcare Country U.S.A. Location NJ Kenilworth Job Description Under the direction of the Director, Sales Planning, the Category Project & Planning Manager is responsible for coordinating the planning and execution of multi-year, brand and retailer business plans for Tier 1 customers for their respective SBU’s. They are accountable for leading the collaborative sales and marketing planning

Clinical Project Manager Job ID: 1185 Location: North Carolina Category: Research and Development/Clinical More information about this job: Overview: The Clinical Project Manager is responsible for providing operational support for the delivery of assigned studies or programs on time and within budget. Primary responsibilities include coordinating and supervising operational aspects of a clinical study, providing guidance for other study team members and collaborating with the Clinical Development team in

Senior Project Manager/Project Manager, Clinical - Biotech Unit- Austin,TX 0801096 Apply Online Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your

Associate Project Manager/Project Manager 1, Lab 0806720 Apply Online Description Quintiles Laboratories is a global Central Laboratory committed to providing fully integrated clinical laboratory services which support all phases of both global and regional clinical trials, while retaining a strong emphasis on patient care. When working with Quintiles Laboratories, sponsors get standardized implementation, analytical testing, and database development and transfer. We have a rewarding opportunity for an

Project Coordinator 1, Lab 0806721 Apply Online Description Quintiles Laboratories is a global Central Laboratory committed to providing fully integrated clinical laboratory services which support all phases of both global and regional clinical trials, while retaining a strong emphasis on patient care. When working with Quintiles Laboratories, sponsors get standardized implementation, analytical testing, and database development and transfer. We have a rewarding opportunity for a Project Coordinator 1

Senior Project Manager - Oncology 0703619 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly, with supporting medical and drug data

Project Manager, Medical Communications 0806529 Apply Online Description Quintiles Transnational is the market leader in providing research, sales and marketing, healthcare policy consulting, and health information management services to the healthcare industry. Quintiles has more than 20,000 employees worldwide and offices in over 50 countries. Innovex Medical Communications, a division of Quintiles Transnational, currently has an exciting opportunity for a Project Manager in our Parsippany, NJ office

Senior Clinical Project Manager/ Clinical Project Manager / Overland Park, KS 0806077 Apply Online Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let

Clinical Project Manager - Biotech - (location flexible - Europe) 0806185 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly, with

Associate Director, Project Management - Cardiovascular - Bathgate, Scotland 0806184 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly

Senior Project Manager - Internal Medicine - Scotland/flexible Europe 0806183 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly,

Manager, Project Coordination Centre, DSMA, Bracknell UK 0806182 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Our leading-edge capabilities provide healthcare companies with the potential to bring new medicines/devices through development and registration to the market place more quickly, with supporting

Project Management Director - Late Phase DSMA 0806164 Apply Online Description When you work for Quintiles you work for the world's leading Pharmaceutical Services Company. We offer product development and commercialisation services to the Pharmaceutical, Biotechnology and Medical Devices industries. Due to continued success in 2007, our division focusing on late phase studies, DSMA (Drug Safety and Medical Affairs), is undergoing rapid expansion. DSMA work with customers on the design and delivery of

Senior Clinical Project Manager/ Clinical Project Manager, Oncology Group, Parsippany, NJ 0806130 Apply Online Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the

Senior Clinical Project Manager/ Clinical Project Manager / Parsippany, New Jersey 0806078 Apply Online Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe

Senior Clinical Project Manager/ Clinical Project Manager / Austin 0806075 Apply Online Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career