Biotech Jobs in Union, New Jersey

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181 Union, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 181
Currently we have a temporary opening for a Facilities Engineer to support a company located in the Short Hills, NJ area.   Responsibilities: Manage major construction projects at multiple North American sites. Developing design concepts with the users and design engineering firm Developing request for proposals to bid projects, coordination with customers, contractors and consultants, Revie...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Clinical and Regulatory Analyst - III Must have: - Bachelor's degree, preferably in nursing, pharmacy or a biological science - At least three years of experience in a hospital, pharmaceutical, or research position. - Prior experience in coordinating and overseeing the production of Aggregate Reports (PSUR, DSUR, PAER etc.) and RMPs required. - PSUR authoring experience would be considered. ...
Outstanding CDM opportunity available with a growing clinical research organization in the Northern New Jersey area. A positive work environment and recognition of the importance of work life balance has led to employee satisfaction and company success. A competitive salary and comprehensive benefits package are offered. Job responsibilities: The Sr. / Clinical Data Manager leads data management...
Hays is currently recruiting for a Project Manager for our global pharmaceutical client located in Northern NJ. This hands-on, process driven Project Manager position is a 6 month contract job. This position is an excellent opportunity to leverage your Drug Development and Regulatory Filing experience in a tangible project-based setting. This position will be responsible for hands-on daily projec...
Support study data management and data cleaning process on an ongoing basis, applying study specific documents and conventions. Identify and issue queries, incorporate query replies, track query status and apply permissible clarifications using the EDC (e.g., RAVE) and related systems (e.g., SAS, jReview, etc.). Assist in documentation gathering and archiving. Minimum 3 years as a Study Data Mang...
Company Confidential Newark, NJ, 07101
Currently seeking dynamic sales entrepreneurs for a unique career opportunity in compounding pharmaceutical sales in the greater Newark area. Requirements · 5-7 years pharmaceutical sales experience · Established relationships with specialists in interventional pain management and/or: orthopedics, rheumatology, neurology, endocrinology, podiatry, oncology and primary care physicians. Preferenc...
Founded in 1977, Lipoid is a globally leading manufacturer of phospholipids for the pharmaceutical industry. Lipoid also distributes phospholipids and botanical extracts and botanical actives made by LIPOID-Kosmetik, a member of the Lipoid Group of Companies. Lipoid is headquartered in Europe and is privately held. Our high-grade products are scientifically developed in Lipoid’s laboratories and ...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Early Clinical Development Specialist - III Must have: - BS degree (will not consider non-degreed) - Direct clinical experience (e.g. nursing) or experience conducting Phase I clinical research in the pharmaceutical industry - Phase I experience with direct tasks of regulatory document authoring (protocols, clinical study reports, IND updates), project management/oversight for Phase I studies,...
Medical Writer/Clinical - III Location: Rahway, NJ OR Upper Gwynedd, PA Must have: Education: Bachelor’s Degree required. RN degree, PhD in health related field and/or PharmD is a plus. Skills: • Must have at least 4 years of medical writing experience within the pharmaceutical industry and at least 2 years of this experience must have been spent authoring clinical documents for regulatory su...
Industry: Pharmaceutical Must have: - BS Life Sciences/Engineering - Experience supporting clinical trials/programs - Experience with Microsoft Project - Experience with Clinical Trial Management Systems such as Spectrum or Impact Responsibilities: · The Clinical Project Specialist will be responsible for supporting and managing the Early Stage Clinical Development functional area planning ...
Responsibilities: · Support the MRL clinical monitors (physicians) who oversee the conduct of Phase I clinical trial. Various therapeutic areas (NON ONCOLOGY) · Lead a team of functional area members through the end-to-end process of PHASE I study conduct (normal healthy volunteer, PK/PD, DDI, ADME, special populations) · Order study related supplies Oversee CRO management for sourced Phase I t...
TechData is looking for Regulatory Specialist, Biostatistician (Some remote), SAS Programmer/Statistical Programmer (Some can be telecommuting), Clinical Research Scientist, Clinical Research Physician, Drug Safety Specialist, Safety Trial Manager, Medical Affairs Contract Manager/Outsourcing manager, Sr. Clinical Data Manager, for our pharmaceutical clients in Central NJ and Northern NJ. Please s...
TechData is looking for Biostatistician, Outcome Research Biostatistician,SAS Programmer/Statistical Programmer (Some can be telecommuting), Translational Operation Manager, Outsourcing Manager, Drug Safety Specialist/Trial Safety Manager, Clinical Study Manager/Clinical Research Scientist, Sr. Clinical Data Manager for our pharmaceutical clients in Central NJ and Northern NJ. Please see below req...
Requirements: -Educated to degree level (biological science, pharmacy, or other health-related discipline preferred), equivalent nursing qualification or other equivalent experience (degree is not required) -Min 5 yrs experience within biotech/CRO or smaller company (can’t just have big pharma exp), would consider experience over degree but depends on background, (high exp working in house, they...
Submissions Coordinator Duration: 5-months Berkeley Heights, NJ Responsibilities: Provides support including, but not limited to, the following for the Global Regulatory Operations team: - Archiving of Health Authority correspondences, MS Word and PDF processing, and document and record management. - Provide MS Word processing support for preparation of regulatory submission documentation. ...
Quality Assurance Specialist Location: Berkeley Heights NJ Duration: 6 months Requirements: -BS in the Sciences or Pharmaceutical related field is preferred with 2-4 years relevant QA experience. -Alternatively, 2 years of higher education with 4 years relevant QA experience may be acceptable. -Good computer skills and working knowledge of common business software -Good knowledge of GMP req...
Great opportunity to join a leading, global medical device technology firm. This position will collaborate with Divisional and Global Regulatory staff to execute the company’s regulatory strategies ensuring successful approval of international product registrations and renewals. Primary Job responsibilities: · Effectively deal with regulatory issues across business units and geographic location...

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