better Biotech Pharma Job at Pharmaceuticals Manufacturers

Supports on a daily basis, Global Clinical Operations (GCO) to facilitate clinical trial operational compliance and process excellence. Core activities include (but are not limited to): - Setting of global quality standards and implementation of global quality management and control systems for global clinical operational processes/activities including vendor qualification and performance management, project management and monitoring for ECREM, SPRI and Global Medical Affairs (GMA) sponsored clinical trials

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

Job ID: RMD092608-25129088 Director, Clinical Research - HPV Job facts: Job function Development Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, our success is built on innovation, curiosity, and diversity – multiplied by 80,000 professionals in 150 countries. As one of the world’s leading research-focused healthcare groups, we’re constantly learning and growing – and seeking people who have those

Position Title: Mgr, Biostatistics I Position Number: 50090435 Department: Research & Development Location: Irvine, CA or New JerseyDescription As the project statistician for assigned clinical programs, the position represents BDMP on project teams advising team members in drug development strategies, plans all aspects of data analysis for assigned projects, has responsibility for the preparation and maintenance of the Analysis Plan (AP), and ensures the quality controlled production of all tables, listings

The person in this role will be focused on systems and will coordinate all aspects involved in initiating, monitoring, and successfully completing reagent and system evaluations with both non-clinical and clinical study aspects. This role is necessary for the organization in order to validate product performance claims, supply data for critical regulatory submissions, define the functional and clinical utility of our products and obtain the opinions and input regarding our products from key opinion leaders

The person in this role will be focused on Point of Care products and will coordinate all aspects involved in initiating, monitoring, and successfully completing reagent and system evaluations with both non-clinical and clinical study aspects. This role is necessary for the organization in order to validate product performance claims, supply data for critical regulatory submissions, define the functional and clinical utility of our products and obtain the opinions and input regarding our products from key opinion

Director Clinical Development Requisition ID: 52179 Position: Full-Time Regular Open date: Dec 5, 2008 10:05:25 PM Functional area: Clinical Location: King of Prussia, Pennsylvania Required degrees: MD Experience required: 5 years Relocation: Not Indicated Basic qualifications: Medical degree (MD or DO) with minimum of 5 years clinical experience Preferred qualifications: Medical Affairs or drug development experience is strongly recommended. Board certification in internal medicine desired. Therapy area

Manager, Clinical Development Requisition ID: 52243 Position: Full-Time Regular Open date: Dec 19, 2008 9:38:23 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: Bachelors Degree Experience required: 5 years Relocation: Not Indicated Basic qualifications: Bachelor's degree Major course of study in a Science or Health related field Comprehensive knowledge of clinical drug development process, policies and regulations Planning and organizational skills Ability to work independently

Director Clinical Development Requisition ID: 51926 Position: Full-Time Regular Open date: Nov 26, 2008 8:47:58 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: Not Indicated Relocation: Not Indicated Basic qualifications: MD Degree, and a minimum of 3 years of industry and /or academic experience required Training in medical oncology, radiation oncology, pediatric oncology or surgical oncology is required. Preferred qualifications: Physician with

Clinical Development Manager, Late clinical Dev., Cancer Vaccines Progr Requisition ID: 50782 Position: Full-Time Regular Open date: Oct 17, 2008 7:19:21 AM Functional area: Clinical Location: Rixensart / Wavre (Belgium), Wallonia Required degrees: Not Indicated Experience required: Not Indicated Relocation: Not Indicated Basic qualifications: Requires a Medical degree, preferably in Oncology. Professional knowledge and skills working with oncology patients and physicians. It is a real added value to have

Director/Manager Clinical Development - Oncology MDC Requisition ID: ONCOLOGY Position: Full-Time Regular Open date: Sep 27, 2006 12:54:37 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: Experience as a Principal Investigator and/or Co-Principal Investigator preferred. Pharmaceutical industry experience highly desirable. We are seeking an Oncologists with deep patient, molecule and disease insight to

Manager/Director Clinical Development - Oncology MDC Requisition ID: 44574 Position: Full-Time Regular Open date: Aug 13, 2007 6:31:53 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: MD degree with Board Certification. Preferred qualifications: MD degree with Board Certification in medical oncology, pediatric oncology or radiation oncology; or experience with supportive care drug develpment; or experience

Manager/Director Clinical Development - Respiratory Requisition ID: 47124 Position: Full-Time Regular Open date: Feb 5, 2008 8:38:37 PM Functional area: Clinical Location: RTP, North Carolina Required degrees: MD Experience required: 2 years Relocation: Yes Basic qualifications: Medical Degree (MD) with demonstrated record of accomplishment in clinical medicine and/or pharmaceutical industry clinical development phases II-IV. Respiratory therapeutic area experience essential. Good communication, influencing

Clinical Development Manager(s), Biologicals Requisition ID: 49639 Position: Full-Time Regular Open date: Jun 9, 2008 3:20:29 PM Functional area: Clinical Location: King of Prussia, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Not Indicated Basic qualifications: MD or PhD with ability to independently evaluate clinical research questions. Sound scientific background required to critically evaluate all scientific aspects of vaccine clinical development and make sound clinical

Director Clinical Development Requisition ID: 47244 Position: Full-Time Regular Open date: Mar 12, 2008 6:17:43 PM Functional area: Clinical Location: Collegeville, Pennsylvania Required degrees: MD Experience required: 2 years Relocation: Not Indicated Basic qualifications: MD Degree, and a minimum of 2 years of industry and or academic experience required Physician with current medical license in the US. Training in medical oncology, radiation oncology, pediatric oncology or surgical oncology is required

Supports on a daily basis, Global Clinical Operations (GCO) to facilitate clinical trial operational compliance and process excellence. Core activities include (but are not limited to): - Setting of global quality standards and implementation of global quality management and control systems for global clinical operational processes/activities including vendor qualification and performance management, project management and monitoring for ECREM, SPRI and Global Medical Affairs (GMA) sponsored clinical trials

Supports on a daily basis, Schering-Plough s Global Clinical Research (GCR) to facilitate clinical trial operational compliance and process excellence. Core activities include (but are not limited to): - Provide process guidance to GCR colleagues within Headquarters functions to facilitate clinical trial quality assurance and compliance with GCP and clinical and operational standards. The areas to be covered include: Global Clinical Data Management, Statistics, Global Scientific Programming, Medical Communications

Description Ethicon Inc. a member of Johnson and Johnson's Family of Companies, is recruiting for a Manager, Clinical Operations located in Somerville, NJ. Ethicon, Inc. develops and markets products for surgery, wound management and advanced wound care treatment . Products are marketed through four divisions: Ethicon Products for precise wound closure and tissue repair; Cardiovations for minimally invasive cardiac procedures; Ethicon Women's Health && Urology for minimally invasive women's health procedures

Clinical Development Associate-Biopharmaceutics Coordinator Location Indiana - Indianapolis Education Required Bachelors Job ID 50339457 Years of Experience 4 Functional Area Clinical Research Expertise Job Type Experienced Job Description For more than 130 years, Eli Lilly and Company has been dedicated to meeting the health care needs of people in the United States and around the world. We address these needs primarily by developing innovative medicines-investing a higher percentage of our sales

DescriptionCentocor Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Director Clinical Research (Oncology/Hematology), located in Chesterbrook, PA or Raritan, NJ. Centocor Research and Development, develops innovative biomedicines. The world leader in monoclonal antibody production and technology, Centocor has brought critical biologic therapies to patients suffering from debilitating immune disorders. The Director Clinical Research is responsible for the development and execution

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

Job Summary Summary:The Associate/Director of Clinical Research reports to the Group Director Early Development and provides medical input to all aspects of product development.Duties:- Deployed to the Emerging Psychiatry team to support mix of psychiatric and analgesia compounds, including the development of appropriate clinical trials and endpoints leading to registration. Additonal support on some late phase compounds as needed.- Serves as a source of medical expertise for product teams and provides input

Description Cordis Corporation, a member of Johnson & Johnson's Family of companies is recruiting for a Director, Clinical Research located in Warren, NJ. 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

Job ID: RMD082908-25095211 Director, Biostatistics and Bioinformatics Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each

Job ID: RMD082208-25095157 Manager, Clinical Research Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other&rsquo

Job ID: RMD071108-25190345 Senior Clinical Research Manager Job facts: Job function Research Location United States - California Pleasanton Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other

Job ID: 40402508457420081119 Clinical Research Associate Job facts: Job function Development Location United States - Indiana Indianapolis Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other&rsquo

Job ID: 00013627 Clinical Research Associate Job facts: Job function Development Location United States - Indiana Indianapolis Company/ Division Diagnostics Schedule Full-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other’s differences

Job ID: 00013500 Clinical Research Associate Job facts: Job function Research Location United States - Indiana Indianapolis Company/ Division Diagnostics Schedule Part-time Job type StandardPrint Who we are: At Roche, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity, and on seeing each other’s differences

Job Summary: We currently have an opening for an Associate Director, Clinical Development, Cardiology in our Edison, New Jersey location. This position will oversee and manage phase 2 and standard phase 3 clinical trials in order to achieve high quality data in a timely and cost-effective manner. Responsibilities: As Associate Director, you will outline clinical development strategy and prepare drafts of Clinical Development Plans and protocol profiles for phase 2 and standard phase 3 trials. You will

Job Summary: Develop study implementation plans and manage operational aspects of clinical trials. Manage interactions with CROs, other external vendors (central/support laboratories and clinical supply/distribution groups), and various non-clinical functions within Daiichi Sankyo, in order to meet company timelines and obtain Food and Drug Administration (FDA) approval of New Drug Application (NDA) submissions. This includes review and approval of budgets, invoices and clinical and regulatory study documents

Description Ortho-McNeil Janssen Scientific Affairs, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Director, Clinical Development CV Franchise, located in Raritan, New Jersey. Ortho-McNeil Janssen Scientific Affairs, L.L.C. is dedicated to providing medical information and consultative support to a number of J&&J's pharmaceutical companies. The company's mission is to create the pre-eminent model of scientific excellence in the promotion of public health. The Director

DescriptionEthicon Inc. a member of Johnson and Johnson's Family of Companies, is recruiting for a Manager, Clinical Operations located in Somerville, NJ. Ethicon, Inc. develops and markets products for surgery, wound management and advanced wound care treatment. Products are marketed through four divisions: Ethicon Products for precise wound closure and tissue repair; Cardiovations for minimally invasive cardiac procedures; Ethicon Women's Health & Urology for minimally invasive women's health procedures

DescriptionOrtho-McNeil Janssen Scientific Affairs, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Director, Clinical Development CV Franchise, located in Raritan, New Jersey. Ortho-McNeil Janssen Scientific Affairs, L.L.C. is dedicated to providing medical information and consultative support to a number of J&J's pharmaceutical companies. The company's mission is to create the pre-eminent model of scientific excellence in the promotion of public health. The Director, Clinical

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

Associate Director, New Product Planning Job Type: Full-Time Location: Cambridge, MA Job Description: This individual will support the Director, New Product Planning in developing the overall marketing and business strategies for Alkermes proprietary products. This person will work closely with the R&D and commercial organizations to lead in the mid-to-late stage development and pre-launch coordination of our proprietary products. These activities will involve initiating, monitoring and analyzing financial

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

Position Title Director, Clinical Research - Gastroenterology / Immunology Business Division Research Institute Country U.S.A. Location NJ Kenilworth Job Description The Director, Clinical Research plays a key role in the design, development, implementation and conduct of clinical trials in the area of Gastroenterology/Immunology, with the initial focus on Crohn’s disease and Ulcerative Colitis. The trials in this area are global in nature (20% travel required) and focus on Phase’s II through IV

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

Title Clincal Research Associate Department Regulatory Compliance Job Type Full Time Job Category Biotechnology and Pharmaceutical Functional Unit Ben Venue Location Ohio-Cleveland City Bedford Our Culture Ben Venue Laboratories, Inc. is a privately held developer, manufacturer, and marketer of sterile pharmaceuticals. Serving the international health care industry with reliable, high quality dosage forms, BVL strives to optimize its return on investment in people, facilities, equipment and applied research

Associate Manager, Clinical Development Job ID: 1178 Location: North Carolina Category: Research and Development/Clinical More information about this job: Overview: The Associate Manager, Clinical Development is responsible for all day-to-day aspects of clinical trials including clinical development, vendor selection and management, coordination and management of data collection, site management and other responsibilities, as required. The Associate Manager, Clinical Development oversees the scientific aspects

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

Job Summary: Develop study implementation plans and manage operational aspects of clinical trials. Manage interactions with CROs, other external vendors (central/support laboratories and clinical supply/distribution groups), and various non-clinical functions within Daiichi Sankyo, in order to meet company timelines and obtain Food and Drug Administration (FDA) approval of New Drug Application (NDA) submissions. This includes review and approval of budgets, invoices and clinical and regulatory study documents

Job Summary AstraZeneca is committed to the discovery and development of novel antibacterial and antiviral agents. As a consequence of progress in Discovery, the Development team seeks another Infectious Diseases trained physician. Description: The role of Senior Director Clinical Research will provide strategic and tactical medical input into the discovery, development and/or commercialization of AZ compounds as well as the use of detailed disease area knowledge to guide translational studies, discovery

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

Job Summary: We currently have an opening for an Associate Director, Clinical Development, Cardiology in our Edison, New Jersey location. This position will oversee and manage phase 2 and standard phase 3 clinical trials in order to achieve high quality data in a timely and cost-effective manner. Responsibilities: As Associate Director, you will outline clinical development strategy and prepare drafts of Clinical Development Plans and protocol profiles for phase 2 and standard phase 3 trials. You will manage

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

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

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

Coordinate the development and documentation of clinical development plans for clinical projects in GPRD as well as detailed project timelines for individual studies. Ensure all clinical programs and studies are appropriately planned according to established parameters. Ensure consistency across all sources of clinical study management including the clinical teams, therapeutic areas, functional groups, and systems (IMPACT, PBR, etc). MAJOR RESPONSIBILITIES: Responsible for implementing and maintaining