The following career opportunities were posted this week at DNAjobs.com. 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
Pharmacoeconomics Manager
(US-New Jersey) Develops, implements and manages a pharmacoeconomics and reimbursement research strategy and assists company in successfully implementing its Biopharmaceuticals' Business Unit growth strategies. Manages the pharmacoeconomic positioning of product and, in conjunction with company and International Marketing, manages the reimbursement feasibility studies for BioPharmaceuticals' products. PHARMACOECONOMICS STRATEGY: Coordinates with company on reimbursement studies during product development and through product life cycle. 'Develops list-price and discount strategies. 'Incorporates pharmacoeconomic rationale into strategic and tactical brand plans and key account strategies. 'Be able to set up and lead a clinical trial from the planning process to using the end results from a pharmacoeconomic perspective. Present pharmacoeconomic abstracts at conferences to support company product portfolio. 'Develops and implements a data gathering process to capture and report HQ pricing guidelines, relevant affiliate pricing, competitor pricing, consumption data and known discounting strategies.
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Postdoctoral Position: Pancreatic Beta Cell Development
(France) A postdoctoral position for up to three years is available in the INSERM group: Development of Endocrine organs INSERM E363, Faculty Necker Enfants Malades, Paris FRANCE Director Raphael Scharfmann The title of the project is: Dissection of signals controlling pancreatic stem cell development. Approaches of cell biology and functional genomics will be used.
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QC Microbiologist (Senior)
(US-Massachusetts) Responsible for all microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrogenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation) Specific Responsibilities: Development and validation of new or improved microbiological methods. Bioburden, sterility and endotoxin testing of raw materials, in-process samples, bulk and finished products and stability samples. Company’s purified water and DI water bioburden, endotoxin and TOC testing as per USP requirements. Identify environmental contaminants. Writing microbiology department related validation protocols, coordinating and/or performing validation and writing validation reports. Establishing databases for microbiological, environmental and validation data. Verifies work of technicians and assists in training.
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Biostatician, PhD preferred
(US-Pennsylvania-Philadelphia) 4-5 years of relevant work experience in Pharma/CRO company. Minimum of a Masters degree in statistics or related area. Strong experience using SAS. DESIRED: PHD in statistics is a plus. JOB DESCRIPTION: Responsibilities will include but not limited to: consulting with in-house staff and outside experts as necessary on the design of clinical trials; writing the statistical section of the clinical trial protocol and the statistical analysis plan; reviewing case report forms; preparing the randomization procedure to be used; representing Client company, if necessary, concerning statistical methodology questions from the FDA or other organizations; extending existing or development of new statistical methods to solve complex problems. Will also analyze data from clinical trials and evaluate the results toward the goal of establishing claims for new drugs or new indications for marketed drugs by ensuring the accuracy and validity of the primary safety and efficacy database, ensuring the accuracy and validity of the analyzed data and preparing accurate, high-quality oral and written reports for the project team, company management, regulatory agencies and investigators.
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BioAnalytical Scientist
(US-Massachusetts) The position will be responsible for early phase clinical product development, optimization, validation and transfer of complex analytical assays to Quality in order to support therapeutic proteins using a variety of methods including protein and carbohydrate techniques. The successful candidate will be responsible for planning and the prioritization of multiple projects in a cGMP environment along with drafting SOP’s, validation protocols and technical reports. Experience:: A Ph.D in Biochemistry, Chemistry or a related field with 2-5 years industrial experience and solid background in the state-of-the-art mass spectrometric techniques, including IonTrap, MALDI-TOF and other MS/MS techniques used to determine detailed structural characterization including post-translational modifications (carbohydrate analyses) of therapeutic proteins.
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Director of Engineering
(US-Massachusetts) The primary function of this group is to provide safe, functional cost effective buildings and equipment in a timely and professional manner. Responsibilities include facilities design, capital planning, project/construction management, technical studies, master planning, identification and remediation for ongoing facility/process issues. The performance of this group directly affects the ability of the business to meet strategic objectives by planning for and providing facilities in a timely and compliant manner while maximizing shareholder value. RESPONSIBILITIES: - Attract, develop and retain talent. - Develop, recommend, and maintain staffing plans to reflect the needs of the client base. - Foster a professional and highly motivated team environment. - Establish and maintain communications with site directors and managers to insure a clear understanding exists of the site's strategic facilities and capital requirements.
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1) Cellular/ Molecular Pharmacologist; 2) Biological NMR Spectroscopist
(India-Karnataka-Bangalore) 1) Cellular/ Molecular Pharmacologist: Job Description Postdoctoral training and experience in animal pharmacology and physiology or in DMPK would be favored. Desired Profile PhD with strong knowledge base and skills in molecular and cell-based methods for pharmacological assays 2) Biological NMR Spectroscopist: Job Description Hands-on experience in 3D and 4D methods are required. A sound understanding of protein chemistry will be a plus. Desired Profile PhD with expertise in protein structure determinations and characterization of combining sites by high field multidimensional NMR. A minimum of 2 years of postdoctoral research.
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Healthcare Staff Positions
(California, Arizona, Washington) For N. CA. I Need: Clinical Nurse Manager for N. CA. 40/hrs BSN and 2 yrs hemodialysis nursing exp. Current CA license as an RN or be able to obtain one. Current CPR certif. (or within 3 months of hire). CNN credential (within one year of hire). R.N. for N. CA. 36/hrs CA registered nursing license or be able to obtain one. Hemodialysis Critical Care exp. and BSN. L.V.N. for N. CA. 36/hrs CA LVN license or be able to obtain one and Dialysis exp. There are sign-on bonuses and some relocation and benefits for these Dialysis positions. For the LA area of CA I need Immunohistochemistry Technician Must have at least 2 years of progressive experience working in Histology and/or Immunohistochemistry as well as record of achievement working in a clinical laboratory. A bachelor's degree in laboratory medicine and ASCP certification. Relocation and great benefit package.
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