Biotech Jobs in Union, New Jersey

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254 Union, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 254
Laboratory technician in precious metal assay services laboratory with leader in the chemical industry. Responsibilities: Will be responsible for performing a variety of classical wet chemical and instrumental analyses. Responsible for the measurement of Loss on Ignition/Drying by instrumental methods. Should be familiar with the techniques of instrumental analysis, to include XRay Fluorescence (X...
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, Review docu...
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. Preferences ·...
Depending on the candidate’s experience level, this role could be filled as Manager up to an Associate Director level. Based on the experience level of the candidate the responsibilities for this role will adjust accordingly POSITION SUMMARY: Under general direction of Xcenda senior leadership, the candidate will primarily design and implement health economic models & research studies. The candida...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Clinical Trial Veterinarian Newark, NJ Full-Time $75,000 - $100,000 Apply Apply Clinical Trial Veterinarian Newark, NJ Full-Time $75,000 - $100,000 Apply Job Details Veterinarian -working on Clinical Trial/Studies Greater New York Metro Area Full-time Permanent position If you are a Veterinarian with Knowledg...
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...
Leading utilities company seeking a RFP/Process Analyst to join their team located in Newark, NJ. This is a long term consulting assignment, approximately 12-18 months long. You will be responsible for handling RFP process from bid to notifying vendors to awarding. You will be responsible for purchase order creation, possible performance of negotiations with help of team members, all dealings in t...
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 a...
We are looking for talented sales professionals in the U.S. interested in joining our success as we grow our company together. The qualifications of an “ideal” candidate would be as follows: • Pharmaceutical/medical device sales experience with documented success • Highly motivated self-starter • Excellent communication and relationship building skills • Understands importance of high level custom...
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...
The Principle SAS Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, listings, figures, and tables) for major, complex clinical projects, acts as a technical expert to offer consulting, training, mentoring for programmers within the group, and may act as a programmer representative on major initiatives. Responsible for the integrity of the programm...
Responsibilities: This individual will be responsible for the collection of data from the LIMS and clinical data set, aligning/merging data sets, apply binding codes, and prepare merged data sets for pharmacokinetic analysis. Generate tables accounting for the disposition of patients and samples, descriptive statistics of pharmacokinetic variables, and results. Generate figures to include but not...
Company Confidential Summit, NJ, 07901
We are seeking a research scientist with proven success at the bench. Possesses a strong understanding of science behind ongoing experiments: the rationale, purpose and appropriate analytical methods. The position holder works virtually independently toward defined objectives conducting several complex experiments, some in parallel, and offering insight into future experiments. The scientist displ...
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...
Qualifications: Minimum of a BS degree Regulatory experience preferred Pharmaceutical/Biological manufacturing or Quality experience preferred Experience preparing CMC (Chemistry, Manufacturing, Controls) post approval submissions preferred Experience with Trackwise and regulatory tracking databases preferred Proactive and highly productive Sound judgment Attention to detail Strong written and ver...
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 submiss...
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. - Exce...
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 tria...
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 sufficient...

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