R & D Jobs in Bridgewater, New Jersey

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227 Bridgewater, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 227
Job Description: 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 in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best in...
Company Description: For more than 130 years, Lilly 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 in research and development than any other major pharmaceutical company. If you are interested in being considered for employment wi...
Company Overview: 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 in research and development than any other major pharmaceutical company. If you are interested in being considered for employment with a “Best i...
Product Manager- RA & Atopic Dermatitis The Product Manager will have responsibility and accountability for the development and implementation of successful strategies and tactics in the context of the launch preparation of dupilumab, a fully human monoclonal antibody targeting the IL4Rα and currently in development for the treatment of atopic dermatitis and asthma. Primary responsibility is to le...
CONTRACT / 6-8 MONTHS.GREAT OPPORTUNITY.URGENT NEED Under the supervision of the project lead statistician, responsible for remove patient identification in the datasets, reformat the data to meet the DataSphere standard. Participate in the working group meeting and provide statistical/programming support to the team. The candidate must have clinical trial experience, knowledge of STDM data and SA...
Company Overview: ImClone Systems LLC is a leader in therapeutic monoclonal antibodies and committed to changing the world of cancer care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of tumor types. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Following its acquisition by Eli L...
Company Overview: ImClone Systems LLC is a leader in therapeutic monoclonal antibodies and committed to changing the world of cancer care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of tumor types. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Following its acquisition by Eli L...
Company Overview: ImClone Systems LLC is a leader in therapeutic monoclonal antibodies and committed to changing the world of cancer care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of tumor types. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Following its acquisition by Eli L...
Our biopharmaceutical client is experiencing a growth in business creating the need to fill a Senior Regulatory Affairs Associate position. The company has a robust clinical pipeline, and now would be an exciting time to get involved in the growth. A competitive salary and benefits package is offered. Our client provides full coverage for a family’s health/medical monthly premiums. Position Requir...
Company Overview: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex, r...
Quality Control Scientist III The QC Scientist will perform routine and non-routine testing with cell-based assays of manufactured in-process commercial and clinical products according to cGMP and SOP’s. Candidate will be responsible for sample chain of custody, sample processing, testing and test data reporting and archiving. Maintain laboratory in an audit readiness stage and cGMP compliant mann...
Description: Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in in...
URGENT NEED.URGENT NEED CONTRACT / 6-8 MONTHS.COULD BE EXTENDED Individual will be responsible for redesigning existing APS.NET web application with SQL back end Will perform all aspects of web development, including requirements, analysis and design, implementation, testing and deployment Skills.5+ Years' experience building Web applications with ASP.NET technologies. Expertise with ASP.NET, .NET...
Minimum REQUIREMENTS: Education: BA or BS degree preferred. Skills: • Must have strong knowledge and skills in Microsoft Office especially with Excel • Strong analytical and communication skills with the ability to summarize results • Previous experience working in pharmaceuticals, preferred • Knowledgeable about Trade or Contract Operations is a plus • Must be able to communicate effectively and...
CONTRACT 6-8 MONTHS.COULD BE EXTENDED.GREAT OPPORTUNITY Must have a science degree and 2+ years working in a pharmaceutical / research environment. Advanced degree in Science or Mathematics. Duties: -Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. -Key responsibilities and skills include, but are not lim...
Duties: -Talks to user to learn procedures followed and source of error. -Answers questions, applying knowledge of the application and procedures. -Talks with coworkers to research problem and find solution. -Talks to technical team to explain software errors or to recommend changes to programs. -May work to find a workaround, when standardized approaches cannot be applied. Skills: -Experienced in...
Job Title: Clinical Trial Manager Location: Bridgewater, NJ Duties: The Clinical Trial Manager will support North America Medical Affairs by managing investigator-sponsored trial operations and ongoing quality improvements in the processing and review of ISTs. The CTM will liaise with field medical teams, medical strategy, legal, and other departments as needed to ensure investigator sponsored tri...
Our biopharmaceutical client is experiencing a growth in business creating the need to fill a Senior Regulatory Affairs Associate/Manager position. The company has a robust clinical pipeline, and now would be an exciting time to get involved in the growth. This would be an ideal position for a Senior Regulatory Associate looking to take their career to the next level. A competitive salary and bene...
Description Job Summary: The purpose of this job is to support the medical writing team with the creation of clinical documentation according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This is a position for an experienced medical writer who also has an interest and capacity to develop new and innovative pro...
Job Title: In-House Clinical Research Associate Position Description Solid knowledge of the processes involved in clinical studies following Good Clinical Practice (GCP) and the Code of Federal Regulations is required. A broad understanding of essential study documentation is critical. The in-house CRA is a key participant in the start-up, implementation, management and close-out of clinical trial...
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