11/24 | CRF Forms Designer – 1 yr. Contract – Top Pharma, New Jersey Summary: An exciting and growing New Jersey Pharmaceutical company is seeking to hire an experienced CRF Forms Designer for a 1 year contract term. This company has a strong pipeline focused on serious disease areas. Location: Nice centralized area of New Jersey commutable from most of Northern & Central New Jersey. Responsibilities: Des | Cornerstone Sear... | | | map | | | action |
11/24 | As head of the Cell-based assay team, this individual will lead a group or 2-3 scientists that are responsible for cell-based bioassays used for the analysis of neutralizing antibody activity of biological based therapeutics in a regulated environment (GLP and clinical). Primary responsibility will be to oversee the development and validation of cell-based assays and subsequent sample analysis of c | Bristol-Myers Sq... | | | map | | | action |
11/24 | THIS POSITION IS BASED IN BANGALORE. ONLY QUALIFIED CANDIDATES WILLING TO RELOCATE TO INDIA WILL BE CONSIDERED. This is a joint venture between two companies to establish a research facility in Bangalore, India that will ultimately house more than 400 scientists to help advance XX’s discovery and early drug development portfolio. Position description : This person will lead and coordinate all aspe | MRINetwork | | | map | | | action |
11/24 | Overview: -Maintain site files, trial master files and study documentation. -May distribute study related materials to sites - protocol, IDB etc. -Will maintain status reports and document quality control. -Review and process regulatory documentation, ensure the execution of clinical trials in a timely, efficient manner, working within established timelines and budgets. -Track clinical trial suppl | Smith Hanley Con... | | | map | | | action |
11/24 | This person will be a member of the Late Phase Group, within Bioanalytical Sciences, BAS, and will be the scientific liaison with internal project teams and with contract research laboratories, CROs, for bioanalytical work which is contracted out on specific projects. Manage two people and three or more projects per person within Late Phase Bioanalytical group that provides oversight to immunoassa | Bristol-Myers Sq... | | | map | | | action |
11/24 | The individual will be a hands-on analytical/bioanalytical scientist working in a highly productive team environment to support drug discovery of small molecules and biologics by collaborating with multidisciplinary groups. The person will be a key contributor in expanding SPS's expertise and capability for large molecule purification and characterization. The following is a summary of the main re | Bristol-Myers Sq... | | | map | | | action |
11/24 | CLINICAL ONCOLOGY PROJECT MANAGER, OPERATIONS Enzon Pharmaceuticals is a biopharmaceutical company dedicated to the discovery, development and commercialization of therapeutics to treat life-threatening diseases. The Company has developed or acquired a number of marketed products, including PEG-INTRON ® , marketed by Schering-Plough, and ABELCET ® , ONCASPAR ® , ADAGEN ® , and DEPOCYT ® , which ar | Enzon Pharmaceut... | | | map | | | action |
11/24 | Senior Manager, Regulatory Affairs: Top Ranked Pharmaceutical Leader, NJ Summary: Our client is a stable and growing larger Pharmaceutical Company. They have one of the top two pipelines in the industry and are always ranked as a top company to work for. They are currently in search for a seasoned regulatory affairs professional to run multiple RA projects across multiple therapeutic areas. You wi | Cornerstone Sear... | | | map | | | action |
11/24 | Adecco Group, a world leader in the recruitment of Technical professionals, has an immediate opening for an Clinical Data Manager on a 6 month Contract opportunity with a leading Pharmaceutical Manufacturer and Distributor in Paramus , NJ . JOB DESCRIPTION In this position candidates will report to Manager, Data Management. Candidates will be responsible for managing data management activities, in | Adecco Engineeri... | | | map | | | action |
11/24 | Senior Manager / Associate Director Regulatory Affairs – DDMAC Location: Trenton, NJ Compensation: $100,000-$130,000 + Bonus + Stock Options to view a VIDEO describing this opportunity Are you your team’s subject matter expert when it comes to all things DDMAC? Perhaps you’re frustrated by lack of opportunity within your current organization? Would you like to be the “Go To” person when it comes t | MRINetwork | | | map | | salary | action |
11/24 | Position ID: 8470SMH Senior Manager / Associate Director Regulatory Affairs – DDMAC Location: Trenton, NJ Compensation: $100,000-$130,000 + Bonus + Stock Options to view a VIDEO describing this opportunity Are you your team’s subject matter expert when it comes to all things DDMAC? Perhaps you’re frustrated by lack of opportunity within your current organization? Would you like to be the “Go To” p | MRINetwork | | | map | | salary | action |
11/24 | 8502SMH Director Medical Affairs Operations Location: Trenton, NJ Compensation: $150,000-$170,000 + Bonus + Stock Options to view a VIDEO describing this opportunity Are you a well-established, savvy Medical Affairs Operations professional? Do you have a solid history of success in the oncology therapeutic area? Perhaps you’re frustrated by lack of opportunity within your current organization? If y | MRINetwork | | | map | | salary | action |
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11/24 | With annual revenues of over $2.5 billion, at Watson Pharmaceuticals (NYSE: WPI) we dedicate ourselves daily to a singular mission, to improve the quality of life for patients around the world through the development and distribution of trusted generic and advanced, specialty branded pharmaceuticals. Under close supervision, performs limited or routine duties in the preparation, review and submiss | Watson Pharmaceu... | | | map | | | action |
11/24 | Associate Director, Regulatory Affairs Operations: Stable and Growing Pharmaceutical Leader, NJ Summary: We are working closely with a Global Pharmaceutical Leader on a key search within their Regulatory Affairs group. They are currently looking for an established regulatory affairs professional to lead the Regulatory Affairs function across life cycle management teams. This position requires a hi | Cornerstone Sear... | | | map | | | action |
11/24 | As part of the Immunochemistry team, this scientist contributes to the development, validation and implementation of immunoassays for analysis of clinical and nonclinical pharmacokinetic or toxicokinetic samples in a regulated environment (GLP and clinical). Primary responsibility will be the analysis of study samples using validated immunoassay methods. Contributes to preparation of validation an | Bristol-Myers Sq... | | | map | | | action |
11/24 | As a member of the Immunochemistry Biomarker team, this scientist will contribute to the implementation of immunoassays for analysis of biomarker concentrations in clinical samples in a regulated environment (GLP and clinical). Primary responsibility will be the development and validation of biomarker immunoassays and subsequent sample analysis of clinical study samples. Contributes to the prepara | Bristol-Myers Sq... | | | map | | | action |
11/24 | As part of the Immunogenicity team, this scientist contributes to the development, validation and implementation of immunoassays for analysis of immunogenicity in clinical samples in a regulated environment. Primary responsibility will be the analysis of study samples using validated immunoassay methods. Contributes to preparation of validation and other analytical reports, BAS sections to the cli | Bristol-Myers Sq... | | | map | | | action |
11/24 | As a member of the Immunogenicity team, this scientist will lead a group of 1-2 scientists that are responsible for the development, validation and implementation of immunoassays for analysis of immunogenicity clinical samples in a regulated environment. Responsibility will include interfacing with teams in the development of assays for new biologic drugs. Will be responsible for reporting study s | Bristol-Myers Sq... | | | map | | | action |
11/24 | As a member of the Immunochemistry team, this scientist will lead a group of 1-2 scientists that are responsible for the development, validation and implementation of immunoassays for analysis of drug concentrations in non-clinical and clinical samples in a regulated environment. Responsibility will include interfacing with teams in the development of assays for new biologic drugs. Will be respons | Bristol-Myers Sq... | | | map | | | action |
11/24 | Develops, validates and implements complex LC-MS/MS assays for analysis of clinical and non-clinical pharmacokinetic or toxicokinetic samples in a GLP-like or GLP environment with self-initiated consultation with supervisor. Represents Bioanalytical Sciences on project teams (IDT, ECRT, PCO Development teams, etc.) and develops strong working relationships with DMCP, DSE and other groups. Prepares | Bristol-Myers Sq... | | | map | | | action |
11/24 | Paramus, NJ currently has an opening for a Senior/Principal Scientist with PK/PD expertise to be part of the multidisciplinary small molecule drug discovery program in psychiatry and neurological disorders. The position ensures PK and PK/PD input for project teams from target validation to development candidate nomination. The candidate is also expected to lead the in vivo PK group and the positio | Lundbeck | | | map | | | action |
11/24 | Integra LifeSciences Corporation is a world leader in developing and marketing high quality surgical instruments, as well as innovative devices and products for use in neurosurgery, reconstructive surgery, general surgery and soft tissue repair. Integra has increased revenues over 40% annually over the last 10 years. We anticipate our significant growth to continue as we celebrate 20 years of clin | Integra LifeScie... | | | map | | | action |
11/24 | Integra LifeSciences Corporation is a world leader in developing and marketing high quality surgical instruments, as well as innovative devices and products for use in neurosurgery, reconstructive surgery, general surgery and soft tissue repair. Integra has increased revenues over 40% annually over the last 10 years. We anticipate our significant growth to continue as we celebrate 20 years of clin | Integra LifeScie... | | | map | | | action |
11/24 | Integra LifeSciences Corporation is a world leader in developing and marketing high quality surgical instruments, as well as innovative devices and products for use in neurosurgery, reconstructive surgery, general surgery and soft tissue repair. Integra has increased revenues over 40% annually over the last 10 years. We anticipate our significant growth to continue. In 2005, 2006, and 2008 Integra | Integra LifeScie... | | | map | | | action |
11/24 | Contract Clinical Study Designer (Data Management) North NJ, Major Pharmaceutical firm 1 year contract, pay rate per hour up to $85.00 phr depending on experience. Description: Development and support of Global Clinical Data Management Systems. Plan and coordinate database design, development, implementation, maintenance, and user support of clinical study database in EDC or paper based trials. Pr | Clark Davis Asso... | Job location not... | | | | salary | action |