DNAjobs.com is proud to feature the following jobs posted July 31 - August 7. For each position, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason Skie
Project Manager and Software Developers (3 positions)
(India-Karnataka-Bangalore) Young and dynamic clinical research company is looking for driven IT professionals to work on cutting edge clinical and laboratory information systems development projects. Should be self motivated and be able to handle startup pressures. Knowledge or experience in pharma and biotech is a plus. Job involves developing an integrated clinical and laboratory system, integrating clinical data with molecular biology and genomics results.
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Quality Control Manager
(India) Job Description: Analysis, Characterization & QC Testing of Biological. Bacterial virus Testing. Ensuring Regulatory & Technical Compliance. Education Required: Masters. Type of Position: Full-Time Permanent.
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Postdoctoral Associate - Mouse Genetics
(US-California-San Diego) A Postdoctoral Associate position is available in the GNF Mouse Genetics group. Projects include characterization and identification of novel mutant mice developed in a mutagenesis screen, QTL analyses, haplotype analyses, development of new animal models of disease and translational research between mouse and human genetics.
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Postdoctoral Associate - Genetics
(US-California-San Diego) We are using forward and reverse genetics technologies to understand the molecular basis for new therapeutic strategies. ENU forward mouse genetics, reverse mouse genetics, human genetics, analysis of gene and protein expression, and cell-based gain and loss of function screens are used in programs in immunology, cancer, and metabolic disease.
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Laboratory Coordinator - Laboratory Operations
(US-California-San Diego) Under direction of Head of Laboratory Operations, help to organize, manage, and maintain a space-limited Chemistry and/or Life Science laboratory. Make adjustments to space to accommodate incoming equipment and staff as necessary. Help to keep scientific staff informed of Lab Operations issues.
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Project Manager - Scientific Solutions
(India-Bangalore, Delhi, Mumbai) Educational Qualifications: MBBS, M. Pharm ( preferably Pharmacology) or Masters in Life Sciences (Biochemistry/Microbiology/Physiology) with a Marketing degree from a reputed institution. Experience: 2-4 years of experience in Clinical Research, Medical Services or Marketing related functions preferably in pharmaceutical companies.
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Technology Lead - Informatics
(India-Karnataka-Bangalore) Educational Qualifications: B.E./B.Tech/PhD. Experience: Experience in Database development, Statistical Modeling, Data mining and data integration projects. Skills: Java, PERL, XML, RDBMS. Location: Bangalore Remarks: Project focuses on integration of large-scale disparate biological databases.
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Animal Technician
(US-Washington) Provide general husbandry of laboratory animals to include: Cleaning the facilities, operate laboratory equipment. Provide some technical support to pre-clinical staff. This position will be responsible for working shift work which includes weekends and holidays.
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Analytical Development - Research Associate / Technical Scientist
(US-Washington) The Analytical Development and Validation division of ICOS QC is seeking an energetic and experienced problem-solver to lead the analytical package development and validation efforts for NCE Drug Products.
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Research Associates - Formulation Development
(India-Tamilnadu-Chennai) The selected persons will be part of a team involved in new product development. Department: R & D Location: Chennai Experience: The candidate shall have work experience in developing formulations for hair care and /or skin care products for a minimum period of 3 years. Qualification: Post graduate degree in any branch of chemistry.
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Head Analytical Chemistry
(France) The candidate should be able to quickly understand the needs and problems of a small, dynamic start-up company. He/she will work independently, but in close collaboration with the medicinal chemistry team, develop analytical methods to measure purity of compounds and implement operationally the analytical facilities.
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Project Manager - Software & Technology
(India-Karnataka-Bangalore) Educational Qualifications: B.E./B.Tech. Preferably Computer Science. Experience: Atleast 2+ plus years of total experience in project management and 4 Yrs of software development experience is essential. Skills: VB 6.0, ASP, COM, C++, XML, MTS, RDBMS.
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Scientific Information Specialist
(US-District of Columbia-Washington/Metro) Provide technical support to users of GenBank, the National Institutes of Health (NIH) DNA Sequence Database, and the other molecular biology database services provided by the National Center for Biotechnology Information (NCBI) at NIH.
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Manager - Clinical Performance, Europe
(UK) This is very much an international role, and you could be managing people remotely, based in a number of European countries, so the ability to thrive in a fast paced global environment is essential. In addition to the line management aspect of your role, you might also be asked to take some project responsibility, so the ability to take the clinical lead on a study is essential.
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Clinical Research Associate / Senior Clinical Research Associate
(Czech Republic) You will be primarily tasked to set up and monitor clinical trials conducted in the Czech Republic as part of international projects. With a life sciences degree or nursing qualification and at least one year experience of Phase II to IV trials, you will have in depth knowledge of FDA and ICH GCP requirements.
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Clinical Research Associate
(South Africa) You will be primarily tasked to set up and monitor clinical trials conducted in South Africa as part of international projects. You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service.
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Toxicologist
(US-Washington-Seattle) The Toxicologist will work in the preclinical development program to support preclinical GLP and non-GLP animal studies intended for IND and NDA submissions. The incumbent will work with the project team(s) to coordinate the preclinical studies to support the schedule and goals of the team(s).
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Sr. Scientist - Aerosol Science
(US-Washington-Seattle) This work will focus on the interaction between drug formulations and devices, and involve collaboration with Research and Manufacturing groups as well as external formulation development and testing contractors. Lead the development effort to optimize formulations for the chosen delivery system for respiratory products.
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Clinical Project Director
(Anywhere-Telecommute) Responsibilities include: overall accountability for the timely and cost effective completion of projects; manage Clinical Trial Managers and Senior Clinical Trial Managers assigned to projects; provide support and leadership to direct reports; monitor project profitability; develop and maintain close working relationship with project management team.
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Product Manager
(US-Washington-Seattle) The Product Manager will be a driving force in the launch of a new product scheduled for commercialization in the U.S. sometime in 2006 and will be heavily involved with all aspects of the drug launch. Initial responsibilities will be to support the Marketing Director in the launch of this new product.
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Clinical Data Manager
(US-Washington-Seattle) Define and prioritize resource requirements across projects. Communicate project status and key CDM issues to team and Sr. Manager, CDM. Provide leadership to the CDM group by establishing a collaborative team environment. Supervise and mentor Clinical Data Associates.
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Director - Regulatory Affairs
(US-Washington-Seattle) This position is responsible for the implementation of regulatory strategies for development candidates and products, for providing technical and strategic direction for projects teams, interacting with the FDA, and providing direction to the assigned programs by coordinating all aspects on submissions.
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Clinical Data Manager (2 positions)
(US-Pennsylvania-Philadelphia) Be familiar with and/or have experience and understanding of all tasks and responsibilities related to Clinical Data Management. Be responsible for and determine overall accuracy/completion of CRF abstraction, coding and quality review performed by other Clinical Data Analysts.
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Vice President - Development
(US-Washington-Seattle) The Vice President of Development is responsible for overseeing preclinical and clinical operations; and developing and improving the infrastructure, including quality control, to support drug development from pre IND studies through NDA and Phase IV programs.
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Senior / Principal Scientist
(US-New Jersey) Job responsibilities include conducting and managing in vitro and in vivo experiments, working in a multidisciplinary team, directing junior scientists, and assessing external target technologies for licensing and/or acquisition.
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Director / Sr. Director Clinical Research
(US-New York-Westchester) Reporting to the senior vice president medical affairs, the director medical affairs/clinical research will have primary responsibility for leading, planning, executing and interpreting clinical trials/research and data collection activities for phases I-III primarily in HIV, as well as oncology and supportive care areas.
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Staff Biologist - Merck & Co., Inc
(US-Pennsylvania) The successful candidate will be responsible for developing, validating and performing immunoassays in a GLP compliant environment, aimed at (1) assessing the immunogenicity of vaccine/biologics in in-vivo test models of toxicity and (2) assessing the immunotoxicity of compounds in development.
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Senior Quality Systems Specialist
(US-Massachusetts-Framingham/Worcester) Implements and maintains clinical quality systems policies and procedures within the clinical function. Ensures adherence to corporate quality procedures and Good Clinical Practice. Maintains the relevant quality systems documentation to support the on going clinical trials.
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Senior Clinical QA Manager
(US-Massachusetts) Provides functional oversite to the Clinical QA function in the development, implementation and maintainenance of quality systems, policies and procedures that ensure compliance of the clinical organization to GCP (Good Clinical Practice). Develops, implements and maintains procedures that ensure compliance to all applicable regulatory authorities requirements.
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Sr. Engineer - Cardiovascular Quality
(US-Massachusetts) Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities.
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Regulatory Associate
(US-California-San Diego) Local Candidates Only. We are seeking a competent Regulatory Associate who has experience with obtaining CE Mark status for multiple products in the International market. Review and approve labeling for CE Marked products.
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Regulatory Affairs Specialist
(US-California) Provide regulatory support for market-released products as necessary. Negotiate direct with FDA projects/products at reviewer level, as directed by manager. Assist with maintenance of Regulatory Affairs product flies to support compliance with regulatory requirements.
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Regulatory Affairs Manager
(US-California) The position will focus primarily on the creation, preparation, and approvals of regulatory submissions for products in the US, Europe, Japan, and other markets. Responsibilities: Independent planning, coordination and preparation of document packages for regulatory submissions, including FDA 510(k), IDE, PMA(S), CE Technical Files and Design Dossiers, Shonin and Ichihen, and internal Letters to File.
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Subject matter experts: BREW applications
(India-Chennai, Mumbai, Delhi and Bangalore) Experience in design, development and end-to-end deployment of BREW applications, including location-based services. Good C / C++ development experience on PDAs / handheld devices will also be considered. Candidates should be BE / BTech / MTech (electronics / telecommunications / computer science).
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RF engineers – CDMA 1x/ GSM / GPRS
(India) Experience in one or more of the following areas: wireless network planning, optimisation, benchmarking, drive tests, installation, commissioning and maintenance of BTS / BSC / MSC. Candidates should be BE / BTech / MTech (electronics / telecommunications / computer science).
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Web Technologies
(India) Design and programming experience in Java, J2EE, EJB, JSP, Swing, Servlets, XML, WebSphere and Weblogic.
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