Biotech Jobs in Union, New Jersey

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168 Union, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 168
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...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
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...
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...
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...
This position is responsible for statistical planning and data analysis of Clinical Trials, in particular Early Phase biomarker studies and Clinical Pharmacology trials. Senior Scientist, Biostatistics Rahway, NJ Job # BIO004013 - Requires a solid knowledge of Statistical Methodology, Experimental Design, and some knowledge in computing software and data management. - Knowledge must be suffic...
PRINCIPLE ACCOUNTABILITIES · To support clinical trials at assigned sites including the responsibility of site management by coordinating all activities pertaining to qualification and initiation of and ongoing site support for the clinical trial. · To provide in-service education and training for physicians, hospital personnel and office staff on study related documents and devices in support o...
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...
Manager, Trials Safety Surveillance • To provide excellent safety support to Development and Marketed product studies • To assist medical affairs teams and the lead safety MD in identifying and managing safety concerns • To ensure effective safety surveillance across trials • To draft safety sections of key trial documents Responsible for: • Identifying and assisting in the management of saf...
Requirements: -Minimum 5 years experience within biotech/CRO working in-house performing duties of a CRA -Experience in locking a database is required -CRO/Vendor Management is required -Ophthalmology is plus -Monitoring experience is a plus Responsibilities: 1.Support the trial operation activities in accordance with country specific regulations/GCPs and companies SOPs 2.Responsibilities ...
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...
This position is to cover for a manager who works on 1 compound for the CD&MA Hematology team. This manager is currently the lead for the program and has 2-3 direct reports. Manage launch preparation activities, start-up and planning of a Novartis sponsored study, and coordinate an extensive third party study program. The individual will oversee the entire US clinical program for this compound. ...
Are you looking for a Clinical Research position with a large pharmaceutical company? TechData Service has multiple positions open with many top pharmaceutical companies for positions including Project Manager with quality systems experience, Drug Safety Coordinator, Pharmacovigilence Scientist, Clinical Operations Manager/Project Manager, Scientist, Medical Information Specialist, CRA Monitor, C...

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