Biotech Jobs in Bridgewater, New Jersey

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231 Bridgewater, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 231
Drug Safety Unit (DSU) - Safety Assistant Position Purpose: Execution of local activities relevant to the management of safety data Primary Responsibilities: Monitor and manage dedicated DSU mailboxes Maintain local documentation as required by legislation (including archiving/tracking/retrieval) – lifting of boxes Support the submission and distribution of reports and relevant tracking Support di...
Contract position Will be responsible for study start up and running clinical trials. The Clinical Research Assistant will work to ensure effective and efficient set up, implementation and assistance of clinical research studies ( phase I through IV) activities by providing adminstration, tracking and support for the clinical trial managers. Maybe involved in vendor selections, kick off meetings,...
CONTRACT / 7-9 MONTHS.COULD BE EXTENDED.VERY LARGE PHARMACEUTICAL CLIENT W-2 ONLY. Developing PL/SQL scripts/tools; Develop web tools and reports; Developing, testing, implementing and documenting applications/tools and reports to support business needs. Analyze and resolve issues. Mandatory requirement: - Very strong Oracle PL/SQL skills. Minimum 3 years experience in PL/SQL development - Very st...
Provide regulatory assessment of post-approval CMC changes for assigned FDA approved NDA drug products in accordance with current FDA regulations and guidances using ECC - a Documentum based electronic change control system. Author and compile CMC dossiers for NDA supplements, annual reports, phase IV IND, and DMF (drug master file) annual updates for assigned drug products in eCTD (electronic com...
WHEN WE RECEIVE YOUR RESUME, WE WILL SEND YOU A COURSE ON HOW TO BECOME AN INTERVIEW SUPERSTAR. IT IS FREE BUT IF WE CHARGED THOUSANDS IT WOULD BE WORTH IT. Director - Clinical Systems Pharmacology (RD19319) (RK) Pharmaceutical / Biotech Root of Jobs - Research & Development Full-time United States - New Jersey - Bridgewater Jobs ID - 960324 The Compensation Benefits - Full Relocation Assistance A...
Clinical SAS Programmer 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 incl...
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...
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...
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...
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...
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