DNAjobs.com is proud to feature the following jobs posted February 1 - 7 (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
Pharmaceutical Sales Rep
(US - OPENINGS IN MOST STATES) Effectively sell this international company's products to selected targeted customers within their territory according to Marketing and Sales strategies. Is responsible for achieving sales goals for company promoted product sales within the assigned territory by effectively delivering sales presentations to key physicians, pharmacists, nurses and other paramedical customers that are involved in purchasing/prescribing decisions. This position reports to the District Business Manager of the specific sales territory being covered. External relationships to be maintained are with physicians, pharmacists, nurses and other paramedical customers and current co-promotion partners. JOB REQUIREMENTS: Bachelors Degree required or advanced degree. At least 1 year of pharmaceutical/healthcare sales experience required. Proven track record of results Diabetes product experience preferred. Solid computer skills required (Windows, Word, Excel). Prior computer experience using sales data reporting software required. Ability to travel (25%) required.
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Post Doctoral (ORISE) Position
(US-Maryland) The Laboratory of Method Development and the Standards and Testing Section at the Center for Biologics Evaluation and Research, Food and Drug Administration have Post Doctoral (ORISE) position available to participate in collaborative project aiming a development of microarray- based assays for analyzing bacterial and viral contamination in biological products (sterility test). This study will include analysis and selection of target genes suitable for speciation, design of unique species-specific microarray oligoprobes appropriate for identification of bacterial and viral contamination, fabrication of microchips, PCR amplification of target genes, and assessment of sensitivity and specificity of developed microarrays. The initial appointment is for two years and may be extended to a third year. Salary will be commensurate with qualification and experience of applicant.
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Clinical Data Manager
(US-Massachusetts) The primary responsibilities of the Clinical Data Manager are to ensure the validity of clinical trial data and to format and organize them for medical review and statistical analysis. The Clinical Data Manager also designs data collection instruments, sets up clinical databases, and manages the flow of data to and from the investigative sites. Performs initial manual review of the CRFs in a timely manner. Ensures that the CRFs are transmitted to data entry staff. Monitors timely data entry. Reviews automated validation system output and determines appropriate course of action to resolve data discrepancies according to established SOPs. Codes adverse experience data. Reviews data discrepancies resolutions provided by the investigative sites and enters corrections in the database, as appropriate. Requirements Bachelor degree, preferably in a scientific field. A minimum of 1-2 years of experience in Clinical Data Management in the Pharmaceutical, Biotechnology, or CRO industry. Should be familiar with the major data management functions and the requirements of Good Clinical Practice. Experience with use of personal computers, database management package(s), and a range of software packages necessary. Some programming experience (e.g., SAS) helpful. Should have demonstrated excellent organizational, verbal, and interpersonal skills.
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Manager of Regulatory Affairs
(US-Massachusetts) The Regulatory Affairs Manager is responsible for the support of consumer and hospital business with annual sales over $500 million, with a customer base of approximately 2.5 million people. The site, currently at 500 employees, produces a minimum of 1.6 million meters annually. In addition to manufacturing, the site has research and development (design control) activities, customer support, servicing and complaint investigation activities, all of which involve QARA. Some of the primary goals of this position include ensuring that policies, procedures and processes are in place so that all site activities meet applicable regulations; registration of new products and current product changes with the appropriate country regulatory bodies, and providing regulatory strategy guidance to R &D. Skills/Experience Requirements Knowledge of regulations and standards affecting In Vitro Diagnostics and Biologics/Medical Devices (EN 46000, ISO 13485, FDA Quality System Regulations), including familiarity with other country regulatory requirements.
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Pharmaceutical Project Coordinator
(US-California-San Diego) Strong chemistry background required (1-4 years of college coursework in the sciences or equivalent work experience). Good documentation and record keeping skills are essential. Experience within a class 100 hood and a class 10,000 laboratory are also required. Good organizational and communication skills are necessary. The Project Coordinator is responsible for coordinating and running all processes associated with the manufacture of the customer’s product. This includes communication with the customer, ensuring inventory is available, coordinating the scheduling of the job with management (including the needs of personnel, equipment and space, set-up, formulation, and cleanup). The Project Coordinator is responsible for all associated documentation and that it is completed in a timely manner for the duration of the process. They are to ensure GMP’s, SOP’s, and the manufacturing documentation are followed by all personnel. The Project Coordinator should be able to perform while receiving minimal direction and be able to give some direction to technicians.
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Analytical Chemist
(US) Aerotek Scientific is looking for an Analytical Chemist with a strong background in instrument use and SOP's.
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Regulatory Scientist
(US-New Jersey) Join the team of a well established medical device company that is in search of a Regulatory Scientist. This position is responsible for the development and preparation of regulatory documents for Class II and Class III medical devices. This includes writing pre-clinical tests and reviewing required documentation for submission to domestic and international regulatory affairs. The Regulatory Scientist will work closely with product development, pre-clinical, and CRO teams. QUALIFICATIONS: *Masters degree in Science or Engineering; PhD preferred *Knowledge of federal, state and local requirements applicable to the performance of regulatory affairs for pre-market submissions highly desirable. *Strong product management skills *Experience preparing budgets, supervisory, analytical development, and PC skills *Required knowledge of IDE and 510K forms Competitive salary + bonus.
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PhD Level Organist Chemists
(US-North Carolina-Greensboro) Join a drug discovery facility who utilizes innovative technology to rapidly translate the functional modulation of human proteins into effective and safe small molecules as therapeutics for the treatment of human diseases. Some include: diabetes, cancer, inflammation, Alzheimer's disease to name a few. Ph.D. Chemists candidate will be responsible for synthetic methods development and process optimization for the lead discovery of clinical drug candidates. Candidate will have a thorough understanding of synthetic organic chemistry and traditional medicinal chemistry with 2-5 yrs research experience in medicinal chemistry. Demonstrated ability to plan researdch activities to achieve pronect goals and objectives is essential. Good organizational and communication skills and ability to work in a multidisciplinary team environment are essential.
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Organic/Synthetic Chemist
(US-North Carolina-Greensboro) Candidate will participate in the company's programs within a highly team oriented environment. This position requires BS or MS degree in chemistry or medicinal chemistry, plus 1-5 yrs productive lab experience. Working knowledge of modern organic chemistry techniques including chromatography, HPLC, NMR and MS required.
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Animal Care Taker I,II &III
(US-Maryland-Montgomery County) The Animal Caretaker will be responsible for assisting and maintenance of accurate and detailed experimental animal records. Assist with receipt, stocking and maintenance of all supply inventories. Perform daily animal health surveillance checks and report any abnormal conditions. Understand and follow Standard operating procedures, safety procedures, and quality assurance guidelines for animal care at all levels of biohazard containment.Sanitize and decontaminate all areas of the facility. Assist in the preparation and Perform technical procedures requiring various levels of biohazard containment. Act as team leader for animal caretakers. Maintain and repair animal caging and support equipment. The animal caretaker must assist with the restraing and manipulation of various animal species.
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Clinical Statistician II - A
For more than a century, our client has been working to advance health care for people around the world. They have evolved into a diversified health care company that discovers, develops, manufactures and markets innovative products and services that span the continuum of care from prevention and diagnosis to treatment and cure. They provide total integrated solutions across the health care spectrum for some of the worlds most prevalent medical conditions, including AIDS, cancer and diabetes. Our client, a major pharmaceutical company in Abbott Park, IL is looking for a Clinical Statistician II - A with the following qualifications: REQUIRES 0-3 YEARS EXPERIENCE Provide in-depth statistical expertise in the areas of; experiment, protocol, case report form design, data base structure, and analysis plan; collaborate with the medical groups to complete joint scientific reports and FDA overviews, including review of such reports to ensure accuracy and clarity. May also contribute to the decision for optimal study design and contribute to the proper use of statistical methodologies for a study. Must have clinical research experience and extensive SAS programming skills. MS Statics Preferred (PHD).
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