(US-California) Our client is the world's most comprehensive, broadly based manufacturer of health care products. Their products include services for the consumer, pharmaceutical and medical device markets. They provide scientifically sound, high quality products and services to help heal, cure disease and improve the quality of life. Our client, a major biopharmaceutical company in Fremont, CA is looking for a Clinical Research Associate with the following qualifications: Job Description: 100% review of FUSION I, PROACTION and VMAC Investigator (SF) files: Review Investigator files on a per site basis for CFR/GCP/ICH compliance (not to include data collection documents such as CRFs, but will include some source docs such as drug accountability logs/packing slips/drug requests/acknowledgements, etc). Further review to establish compliance with Scios SOPs and project specific guidelines, monitoring plans, including all versions from study start to finish. The files as reviewed will also be check to ensure chronological order by date and reconciling mis-filings. Spreadsheets will be compiled for each site in Excel identifying issues and a recommended corrective resolution. Major issues will be earmarked for priority reconciliation. Hard copies should be utilized and I would suggest saving an electronic copy if needed, to a CD and not on a shared drive.. Requirements: CRA with at least 2 years monitoring experience and knowledge of GCP regulations to work 40 hours per week until audits complete, but no later than 31 Dec 03. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-California-Los Angeles) General Surgeon. BE/BC. Expertise in Laparoscopic Morbid Obesity a must. Excellent opportunity. Well established surgical practice.
(US-New Jersey-Central) Method development and validation with experience writing validation reports, thorough knowledge and recent hands-on experience using HPLC instruments (HP and/or Waters) with Turbochrome and/or ChemStation data acquisition systems knowledge and hands-on experience performing analysis by FTIR and water determinations by Generation of study protocols and executions Ability to monitor and input data into a specific inventory database for reference standards Handling of controlled drug substances and related compounds. Knowledge of GC, GC/MS, NMR and LC/MS Recent experience using computer programs to include Microsoft Word and Excel Ability to produce quality work with minimal supervision in a Laboratory environment and the ability to multi-task. MINIMUM REQUIREMENTS: BS or MS in chemistry or related discipline. 4-6 yrs. Pharmaceutical experience preferred.
(US-New Jersey-Northern) You’ll use your scientific expertise and leadership capabilities to: · Build, manage and develop a computational chemistry group. · Deliver high quality computational chemistry contributions in the ongoing drug discovery projects from hit identification to delivery of development candidates. · Ensure implementation of a state of the art computational chemistry platform and infrastructure. · Contribute to the strategic planning and development of the Chemistry Department as a member of the Management Team. · Participate in the development of the hit identification platform in a close collaboration between USA and European Collegaues counterparts in Denmark. What We Look For: · PhD in organic chemistry, preferably with focus on theoretical or physical chemistry, PostDoc within relevant research area. · 5 – 10 years industrial computational chemistry experience in drug discovery, preferably within the field of GPCRs and CNS medicinal chemistry. · Experience with hit identification using focused screening approaches. · Track record of significant scientific contributions with publications in peer-reviewed journals and patents. · Experience with effectively managing, supervising or leading other professionals. · Strong interpersonal and influencing skills, and comfort working in a changing environment . Join our multi-disciplinary team of scientists in a stimulating research environment, which offers distinct opportunities to leverage your expertise and work with world-class leaders in this field. We offer a competitive compensation and benefits package consistent with being a part of a global organization.
(US-New Jersey-Northern) You will use your medicinal and organic chemistry expertise and leadership capabilities to: · Build, manage and develop a medicinal chemistry group towards the delivery of high quality drug development candidates · Contribute to the strategic planning and development of the Chemistry Department as a member of the Chemistry Management Team · Participate in the development of the synthetic and analytical chemistry technology platforms. What We Look For: · PhD and PostDoc in synthetic organic chemistry. · 5 – 10 years medicinal chemistry and drug discovery industrial experience, preferably within the CNS and GPCR area. · Experience with all phases of drug discovery from hit identification to delivery of development candidates, using state of the art parallel synthesis technologies. · Track record of significant scientific contributions with publications in peer-reviewed journals and patents. · Experience effectively managing, supervising or leading other professionals. · Strong interpersonal and influencing skills, and comfort working in a changing environment. Join our multi-disciplinary team of scientists in a stimulating research environment, which offers distinct opportunities to leverage your expertise and work with world-class leaders in this field. We offer a competitive compensation and benefits package consistent with being a part of a global organization.
(US-New Jersey) You’ll use scientific expertise and leadership capabilities: · Build, manage and develop a group in the delivery of efficient analytical support of medicinal chemistry activities in the ongoing drug discovery projects. · Ensure the delivery of high quality LC/MS analysis, NMR analysis, mass directed purification of compound series and libraries, HPLC purification of complex mixtures and enantiomers, and physicochemical characterization of new chemical entities. · Implement an efficient and high quality analytical chemistry platform and infrastructure. What We Look For: · PhD and PostDoc in organic chemistry with a strong focus on LC/MS. · 3 - 5 years analytical chemistry experience in an industrial or corporate setting. · Experience in providing analytical chemistry support to a synthetic or medicinal chemistry area. · Track record of significant scientific contributions with publications in peer-reviewed journals and patents. · Experience effectively managing, supervising or leading other professionals. · Strong interpersonal and influencing skills, and comfort working in a changing environment. Join our multi-disciplinary team of scientists in a stimulating research environment, which offers distinct opportunities to leverage your expertise and work with world-class leaders in this field. We offer a competitive compensation and benefits package consistent with being a part of a global organization.
(US) Cutting edge client company is looking for a rare and talented individual to add value to their organization through the superior application of modeling and simulation for optimization of decision-making in drug development. This person will be required to interact with national and international Pharmaceutical and Biotech company project teams in developing optimal clinical development programs and trial designs using pharmacodynamic modeling and simulation. Whoever lands the job will be responsible for all aspects of the projects, including defining key issues in clinical development and trial design, analysis, PK/PD modeling, simulation, interpretation and presentation of results. The Requirements for this position are as follows: You must have a Clinical Pharmacologist/Pharmacokineticist: Ph.D. or have a MD with clinical drug development experience. Solid experience in clinical pharmacology, pharmacokinetics and pharmacodynamics in a project team setting is essential. A strong background and experience in PK/PD modeling with WinNonlin/NONLIN, NONMEM, SAS, or S-PLUS a prerequisite. Strong communication skills are highly desirable. This company is looking for a very specialized and talented individual that meets or beats all of the above requirements.
(US-Connecticut-Danbury/Bridgeport) A enormously growing genetic diagnostics company is in the hunt for an award winning, talented sales star to keep up with the demand for their cutting edge cancer diagnostic screening test. If you are Passionate about changing the world, one person at a time, this could be the chance of a lifetime! Instead of treating people after the develop cancer, our client is helping people avoid developing cancer in the first place. We are looking for people who live in Fairfield, New Haven or Litchfield Counties who have a successful track record of driving new sales. You too could enter the realm of the "Six Figure" earners by joining this team and charting your own course to fulfillment. Not only can you make a great living, but you can be a part of a company that is changing the world by identifying people's predisposition for certain cancers, thus allowing early prevention.
(France-North Pas de Calais) Field: Microarray data and complex genetic disease analysis INSTITUT DE BIOLOGIE DE LILLE CNRS UMR 8090 - Genetics of Multifactorial Diseases Lille - FRANCE A full time POSITION in Biostatistics and Bioinformatics is available for 2 years starting November, 2003 in the Department of Human Genetics - Genetics of Multifactorial Diseases – CNRS UMR 8090 - Director of Unit: Professor Philippe Froguel Project Description: Analysis of Affymetrix microarray data from transcriptome experiments using animal models and genetic data from human polymorphisms typed in both cohort and family studies. This will be carried out in the context of exploration of the molecular mechanisms underlying pancreatic beta-cell dysfunction and associated insulin-resistance. Activities: * Select and set up appropriate statistical methods for analyzing: o Microarray data, including normalization, selection of significant expression variation, clustering, GO annotation o Genetic data, including linkage analysis, association analysis, linkage disequilibrium mapping and haplotype construction * Manage data (acquisition, validation, quality control, organization) * Analyze data, interpret and present results * Adapt or develop new statistical tools when necessary * Optimize usage of such tools and set up standard analysis procedures * Data acquisition from public databases and other online resources Skills: * Knowledge of statistical methods * Experience of statistical software such as SPSS, S+ or R * Strong experience in microarray data analysis * Knowledge of public databases and other online biological resources Experience: Masters Degree (DESS) or PhD, and, ideally, practical experience of microarray experiments. Conditions: The Position is for 2 years, from the 1st of November 2003, in Lille, France, in the bioinformatics and biostatistics team (6 people) of the Genetics of Multifactorial Diseases Laboratory. Training in population genetics can be provided by the lab Application Deadline: Applications will be reviewed in October 2003 until a suitable candidate is identified.
