Dear Life Sciences Professional,
DNAjobs.com is proud to feature the following jobs posted May 1 - 8 (listed in chronological order). 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
Senior Clinical Research Associate II
(US-New Jersey) Responsible for coordinating and supervising all aspects of implementing and conducting clinical studies in accordance with FDA regulations and GCP/ICH guidelines; contributing to the development of protocols and CRFs.
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Sr. Scientist
(US-Massachusetts-Boston) The Group Leader for Purification Process Development is responsible for management of all internal and external activities for development of purification processes for early- and late-stage clinical protein therapeutics (mammalian cell culture-based).
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Senior Separations Scientist
(US-California-San Francisco) There is an opening for a Senior Scientist in the Analytical Sciences Department to develop single- and multi-dimensional separations schemes for high resolution of complex protein and peptide mixtures derived from biological samples.
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Associate Director / Director of Separations
(US-California-San Francisco) Our client has an opening for an Associate Director/Director in the Analytical Sciences Department to develop analytical separations methods for proteins and peptides, and to guide those methods through product development.
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Pharmacy Tech II - B
(US-Illinois-Chicago) Our client is looking for a Pharmacy Tech II - B with the following qualifications: Under the direct supervision of a registered pharmacist, compounds and dispenses medical prescriptions. May be expected to perform some clerical duties relating to the department.
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Research Associate - Cancer
(France) With the equivalent of an undergraduate degree in Biology, the successful candidate will hold a French Level 2 certificate in animal experimentation including a few years professional experience in this area.
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Head of Business Development
(France) With a life science background, and a successful experience in business development with pharmaceutical and biotech companies. The Head of business development will develop technical and commercial partnerships in an international environment.
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Bioinformatics Programmers
(India) Our objective is in translating technology advantage into biological research benefits. If you want to be part and source of Helix DNA, your genetic sequences must be thoroughly mixed with hard core C/C++ programming on windows and Linux platforms.
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Research Associates and Student Trainees
(India) We are currently building our Life sciences research factory involving Research scholars, Associates, Student trainees for participating in the R&D projects and to further our research services ambition.
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Research Technician
(US-Ohio) A full-time position for a research technician is available in a developmental neurobiology laboratory at the Medical College of Ohio. This person will join our lab to assist in studies in specification and differentiation of neural crest-derived neurons.
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Scientific Support Specialist
(Canada) As a scientific support specialist your primary responsibilities will include: Daily interaction with customer base. Supporting client specific scientific queries. Creating customized software solutions.
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Senior Quality Assurance Associate
(US-California-San Francisco) The main purpose of this job is to assist in implementing, facilitating the Quality Assurance (QA) controlled system for clinical/commercial products. Assist in vendor qualification activities and vendor auditing for drug and device.
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Senior Clinical Research Associate
(US-California-San Francisco) Ability to handle internal and external aspects (monitoring/administrative) of a multi-center phase trials from study initiation to completion/close-out. Coordinate writing of protocols and protocol amendments.
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Postdoctoral Position in Visual Neuroscience and Biophysics
(Finland) A three year post-doctoral position in neurobiophysics is available at University of Oulu, Dept. of Physical Sciences, starting in August 2004 at earliest (starting date is negotiable).
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Postdoctoral Fellow in Computational Systems Biology
(Singapore) One postdoctoral position is available (three-year contract, renewable) in the Systems biology group, Bioinformatics Institute in the area of computational cell biology.
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Product Manager Structural Biology Systems
(Netherlands) Seeking a dynamic individual to plan, actively pursue and supervise introduction of our instrumentation to the macro-molecular community in Europe and Asia. This person will be responsible for pre and post technical-scientific sales support of these systems.
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Post Doctoral Position - Software Engineering
(Netherlands) For its participation in the Cyttron biological cell microscope project, Bruker Nonius is seeking two people for a three year postdoctoral project.
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Research and Development
(Canada-Quebec-Montreal) Researching and implementing solutions to problems in computational chemistry. Developing and implementing computational methods, 3D graphics, and user interfaces through the full software life cycle of design specification, implementation, and testing.
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Sr. Manager, Business Development
(US-Washington-Seattle) Evaluate scientific and financial feasibility of pharmaceutical licensing oppsortunities. Perform patent interpretation and analysis. Negotiate licensing opportunities.
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Sr. Investigator - Virology
(US-New York-Westchester) Direct group responsible for discovery of novel antiviral agents. Develop biochemical, pseudoviral and whole-viral screens against novel targets. Source and oversee installation of automation equipment and software for data analysis and management.
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Product Manager
(US-Washington-Seattle) Initial responsibilities will be to support the Marketing Director in the launch of this new product. These responsibilities will include development of all tactical plans associated with the launch as well as input into strategic plans for the brand.
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Associate Director, Manufacturing Sciences
(US-New York-Westchester) Develop and implement strategies for development of up-stream manufacturing processes for all biologic products. Design experimental studies to optimize processes for recombinant mammalian cell culture in suspension, fed-batch bioreactors.
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Vice President, Development
(US-Washington-Seattle) 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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Associate Director QA
(US-New York-Westchester) Develop and execute plans to provide QA oversight of in-house and outsourced manufacturing activities to meet project goals. Prepare CMC documentation to meet project goals. Serve as technical expert to direct Company’s programs in biologics and small molecules.
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Sr. Clinical Research Associate
(US-Washington-Seattle) This position works directly with the Clinical Trial Manager and Senior Medical Director to coordinate research and administrative strategies for the management of clinical trial research.
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Sr. Financial Controls Analyst
(US-New York-Westchester) Hands-on responsibility for all preparation, planning, and execution for compliance initiatives; developing, monitoring, auditing and reporting of compliance to executive management, assisting CEO & CFO with their financial statement certification.
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Computer Validation Specialist
(US-Washington-Seattle) This individual will work with department heads and Quality assurance to develop and execute computer system validation plans. Develop validation documentation including: Validation plans, User requirements, Risk analysis, IQ/OQ/PQ protocols, Summary reports, and Standard operating procedures.
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Director / Sr. Director, Clinical Research
(US-New York-Westchester) The Director of 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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Sr. Scientist Subject Matter Expert
(US-Illinois-Chicago) The day-to-day work will be scientific evaluation of new test leads, prototyping of new assays, providing technical review of assay development projects, and communicating with consultants/external experts.
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Director / Sr. Director, Clinical Research
(US-Washington-Seattle) With guidance from senior management, develops the tactical clinical trials programs to achieve the company’s strategic development objectives and the successful registration of new products in a timely and cost-effective manner.
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Associate Director Regulatory Affairs - Biologics
(US-New York-Westchester) Organizes, reviews and prepares/files INDs. Maintains INDs in current state. Organizes pre-IND meetings and FDA communications. Participates in Project Teams. Interfaces with R&D, QA, QC/AD, and Mfg to identify CMC requirements.
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Director, Cardiovascular Research
(US-Maryland-Baltimore) Responsible for developing strategies and solving problems across diverse functional areas of the business, e.g. clinical medicine, clinical operations, biostatistics, data management, regulatory affairs, and marketing.
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Vice President, Regulatory Affairs
(US-New York-Westchester) Supports the Company’s clinical development program by developing regulatory strategies for registration and assuring compliance with FDA and ICH Good Clinical Practice requirements.
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Clinical Research Scientist
(US-Maryland-Baltimore) Independently design and report clinical trials (Phases I, II, and III) within a clinical program. As a team leader you will provide strategic leadership for your team such that the team completes corporate objectives on time and within budget.
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Senior Manager, Drug Disposition
(US-New York-Westchester) Lead the design and implementation of preclinical studies to evaluate drug disposition including absorption, distribution, metabolism, and elimination of the Company’s drugs in development. Manages and analyzes data sets of PK and TK information and for preparing technical reports.
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Clinical Project Manager
(US-Pennsylvania-Philadelphia) Key Responsibilities: Serve as primary contact between sponsors, project team and functional groups to track progress and ensure that all project goals are accomplished. Provide accurate weekly updates on the progress of the project.
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Sr. Director Regulatory Affairs
(US-Massachusetts) Our client, a research based pharmaceutical company in the Boston area, has a need for a Sr. Director of Regulatory Affairs-Marketed Products who has experience with/of the FDA's Division of Drug Marketing, Advertising and Communications.
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Senior Project Manager
(US-Massachusetts-Framingham/Worcester) The senior project manager is responsible for coordinating a multidisciplinary project team to assure the accurate and timely completion of all contracted activities.
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Sr. Clinical Project Manager
(US-Massachusetts-Boston) A leading research-based pharmaceutical company has an opening on their clinical team for a Sr. Project Manager who will provide input for product development planning, produce clinical protocols, and will perform timeline management and tracking of projects.
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Human Resources
(US-Washington-Seattle) This position will partner with senior management to align HR strategy and tactics with growth and change objectives for the organization. A thorough knowledge of transforming an organization both culturally and organizationally is essential.
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Project Management
(US-Massachusetts-Boston) Responsible for oversight and coordination of operations within Clinical Affairs and Project Management for all activities associated with the management of Clinical programs.
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Chief Financial Officer
(US-Florida-Miami) Looking for a CFO for a biotech company that is looking to go public by year's end. Looking for Pharm or biotech industry experience. Looking for someone who has taken a start-up or growing company public.
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Project Manager / Associate Director Project Management
(US-California-San Francisco) We are actively seeking a motivated project manager to assist in the scientific collaboration of 1 to 2 R&D projects.
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Lab Director Virology
(US-Maryland) Direct lab activities, solid scientific knowledge in virology, demonstrated management and supervisory experience, excellent organization and communication skills, working knowledge of regulations.
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Clinical Project Manager
(US-Washington-Seattle) The successful candidate will be responsible for the effective management and execution of clinical trials from protocol development through completion of the final study report.
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Sr. Clinical Trials Manager
(US-California-San Francisco) CRM is responsible for coordinating the monitoring and collection of high quality clinical research data from the sites and ensure its proper transmittal to the data management group.
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Manager, Regulatory Affairs - Small Molecule
(US-New York-Westchester) Support the Director Regulatory Affairs in the preparation, submission and maintenance of the MNTX Inj e- NDA, including the interface with external contacts. As assigned, this individual would also be the Regulatory responsible person for one or more INDs and planned MNTX post approval S/NDAs and other planned NDA submissions.
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Manager, Regulatory Affairs
(US-Washington-Seattle) Provides strategic direction for clinical regulatory issues and supports tactical functions at the project level. Manages the preparation of regulatory submissions (US & ex-US) and provides clear and consistent regulatory recommendations to product teams for responsible projects.
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Clinical Microbiologist
(US-Washington-Seattle) The Senior Manager/Assoc. Director of clinical microbiology is responsible for overseeing the microbiology aspects of the clinical development programs.
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Vice President - R&D (Bulk Drugs)
(India) Candidate should have lead a large team/teams of at least 40-50 persons working on different projects and should have hands on exposure to generic research,process development. Exposure to NCEs work is desirable. Exposure to contract research /custom synthesis would be an added advantage.
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Medicinal Chemists-Research Associates (Multiple Openings)
(US-Massachusetts) A productive synthetic chemist, well-versed in modern synthetic methods and spectroscopy techniques, who will work closely with scientists in medicinal chemistry to plan and execute syntheses of compounds required in lead identification and lead optimization programs.
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Formulation Scientist
(US-Massachusetts) A high performance, self-motivated researcher with a PhD in pharmaceutics or pharmaceutical sciences will be required to develop oral formulations for small molecule therapeutics. Industrial pharmacy experience is preferred.
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Toxicology / Preclinical Scientist
(US-Massachusetts) The candidate who fills this position will be involved in registration-enabeling preclinical studies to support lead candidate development for both biologic and small molecule development programs.
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Formulation Scientist
(US-Massachusetts) Develop and characterize formulations to support small molecule drug discovery and development programs. The position requires hands on laboratory work. Establish a formulation development and testing lab.
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Associate Director Protein Engineering
(US-Massachusetts) Associate Director will be responsible for leading a team of 10-12 Scientists who are responsible for the development of second generation therapeutic proteins using a variety of methods including protein and carbohydrate modification, and conjugation techniques.
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Executive Director Preclinical Development
(US-Massachusetts) Direct a pre-clinical department in the areas of toxicology, pathology, drug disposition and metabolism, bioanalytics, pharmacokinetics, and pharmacogenomics.
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Medical Director-Clinical Development
(US-Massachusetts) Currently we have several companies searching for just the right person to lead their clinical development team. Areas of interest are numerous but could include Oncology, Neurology (drugs or devices), Cardiovascular (drugs or interventional) and Infectious Disease are some of the areas.
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Director of Clinical Affairs
(US-Massachusetts) The Director of Clinical Affairs will be responsible for all aspects of clinical trial management. These responsibilities include the management of contract research organizations (CROs), design and writing of protocols and clinical trial reports, preparation and monitoring of budgets and trial timelines, and recommendation on resource requirements.
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Clinical Program Manager
(US-Massachusetts) The (Sr) Clinical Program Manager works within the Department of Clinical Operations to manage clinical studies that are designed to establish the safety and effectiveness of Company's products. This person initially will focus on early clinical development, but will have the ability to bring one or more of these products to Phase III development, as necessary.
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