DNAjobs.com is proud to feature the following jobs posted Jan 17 - 24 (listed in chronological order). For each position, I have listed a short description and a link for more information.
This week's newsletter also features a career coaching lesson from Cindy Kraft, titled "What Kind of Car Are You?"
As always, I wish you tremendous success in your searching!
Jason
Contract Recruiter
(US-Mississippi) Our well respected client is seeking (2) Contract recruiters . This opportunity can last from 4 months and longer ... The last contract recruiter was there 18 months. RESPONSIBILITY: The experienced recruiter will source and manage the full cycle recruitment process for a targeted region. The contract will last approximately four months. JOB REQUIREMENTS: Two years of progressive recruiting experience, preferably in pharmaceutical sales. Must be strong in: developing relationships with managemet, partnering with HR Generalists, sourcing (AIRS certification is a plus), working with an ATS system and proven experience with diversity recruitment strategies. Bachelor's degree or a Five years of related experience. Excellent Pharmaceutical Company. Only qualified candidates will be contacted.
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Pharmaceutical Sales Rep
(US) Contemporary Careers, Inc., is a leading staffing organization and Career Coaching provider. www.contemporarycareers.com. We are experiencing MAJOR expansions with our clients !!!! OPENINGS IN MOST STATES Albany NY, Boston MASS, Bulter PA, Lancaster PA,Columbus OH, Huntsville AL, Portland OR, Salem, Utica/Rome NY, Wilmington NC .. and more.. Boston North-- Boston, Cambridge, Salem, Waymuth and Butler, PA JOB DESCRIPTION: RESPONSIBILITY: Effectively sells 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.
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Tech Applications Support
(US) Great long-term contract positions! A large well known consulting company is looking for experts in applications support. You will support the WIF (Workflow, Imaging, Fax) application, a customized off-the-shelf Integic product used to manage images for drug studies. You’ll provide systems monitoring, maintenance, and administration. Looking for a self-starter with the ability to communicate effectively and perform as part of a dynamic team environment. You need to be able to problem-solve issues in the NT server (Windows 2000 server) environment. And also in the Citrix environment. Must be able to understand reported client issues, translate those client reports into application issues, and correct the application issues quickly and efficiently. Must also be able to work effectively in both remote and on-site application support environments. Skills Needed: Windows NT Server Windows 2002 Server Citrix Visual Basic Integic (a must for one position, a plus for another) Oracle Must have a green card or be a US citizen. Must be willing to travel 70-90% of the time. Locations include traveling to Chicago, Kalamazoo, or New London.
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Medical Device Sales Representative
(US-Massachusetts-Boston) This position will require a 24/7 commitment , the sales rep will be expected to be in surgery to answer any technical questions for the surgeon, nurses and patients before , during and after surgery. Developing relationships with orthopaedic surgeons, OR administrators as well as Procurement Directors. Lots of relationship building , ie: golf outings, fishing trips, sporting events. Supply technical assistance and advice to the surgeons.
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Director of Clinical Affairs
(US-Minnesota-Minneapolis) Join a global leader in the orthopedic medical device industry as the new Director of Clinical Affairs. This position will report to the Corporate Director and be responsible for clinical study design, implementation, monitoring, data collection and the FDA regulations that govern these functions. The Director will interact with physicians/clinical investigators, trial coordinators and regulatory agency personnel as the internal clinical affairs representative and will direct the preparation of clinical results for pre-market approval applications. REQUIREMENTS: Scientific or technical Bachelor's Degree; Master's preferred; 8+ years experience in Regulatory/ Clinical Affairs/Quality Assurance as it relates to medical devices; Prefer a background in orthopedic/ neurological implants; 4+ years supervisory/management experience; Extensive experience with regulatory and compliance issues; Working knowledge of 501k, IDE, and PMA documents; Good PC, oral/written communication and problem solving skills Competitive salary based on experience, bonus, benefits and relocation assistance.
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Bio-Assay (Mammalian Cell)
(India-Andra Pradesh-Hyderabad) We are one of the of the leading manpower pharmaceutical consultants based in India working for top pharma companies like Dr. Reddy Laboratories, Dabur Research Foundation, Wockhardt Research Centre, Torrent Research Centre, Reliance Life Science, Vitalife Labs (Part of Apollo Tyres), Jubliant Organosys, Cipla, Matrix Laboratories, Winmedicare, Panacea Biotech, Zenotech, Nagarjuna Fertilizers and Chemicals Limited, etc., to name a few. At the present outset we are looking for people who has 1 to 3 years of experience in doing bioassays in mammalian cell lines for one of clients. The company operates both from India and USA. The minimum qualification is a Masters degree. Please apply within one month from the date of this advertisement.
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Clinical Medical Services Specialist - B
(US-Illinois) 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. REQUIRES 3-5 YEARS EXPERIENCE - Provides medical support with emphasis on the intake of medical product experiences and processing standard communication requests. Acts as a liaison with Quality Assurance for product quality problems where an adverse event is involved. Works with Customer Service to provide standard information and product replacement as necessary. Provides assistance to the medical and lay community with standard information that is from the package insert or information from the standard letter database that deals with labeled and specific off-label information/indications. BS Preferred. BSN Highly Desired.
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Chemist Collaborator
(Work from Anywhere) An Organic Chemist is needed for a collaboration effort to synthesize research amounts of a subsituted amino acid. All equipment and most chemicals can be provided but the chemist must have his or her own lab space. The goal is to get FDA "orphan" status for this remarkable compound. The formula has already been acquired and I will agree to sharing a percentage of any revenues in exchange for the work that will be involved. This has been a long term effort and I'm interested in hearing from any organic chemist who might be interested.
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Up Stream - Process Scientist
(US-Massachusetts) SciGenium is looking for an Up Stream - Process Scientist in the Boston Area. Responsibilities: Process scale-up of a Mammalian cell facility for a recombinant Protein - product. Emphasis is on upstream process development work i.e. BioReactors- perfusion, aspiration. Previous experience growing the cells cleanly and efficiently up to 500 liters as well as downstream purification. Work in a Scale-up manufacturing environment operating under cGMP as well as experience from process transfer to Manufacturing. Utilize your knowledge of purification development principles for polysaccharides as well as ability to perform routine in-process and release assays. Work with Bioreactor to created biologics, purified proteins and ability to assist in cell / tissue culture as well as associated knowledge/technology transfer issues. Will perform protein characterization via spectroscopy (FT-IR, CD, fluorescence, or Raman). Requirements: Phd and 5+ years commercial exp in accordance with cGMP and FDA guidelines Good working knowledge of SOPs, GLPs, and SSPs.
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Regional Account Manager - Instrumentation Consumables
(US-Massachusetts) SciGenium is currently searching for a Regional Account Manager –Instrumentation Consumables , New England Region. The ideal candidate should have: 1-2 years experience in selling scientific instrumentation or consumables; Experience selling into the life science market both academic institutions & pharmaceutical firms; Ideally a strong background in hands on Analytical Bench Chemistry, with HPLCs and various columns; Trained/skilled in organizational and account based selling strategy Qualifications: BS in Chemistry, or biochemistry; Ability to generate leads and travel 70% of the time. Start-up style selling experience & an established book of business is ideal.
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Clinical Trials Manager
(US-Massachusetts) Clinical Trails Project Manager who will work as company representative on phase 2 and 3 clinical trials. Will manage and work with CROs (Clinical Research Organizations) and CRAs (Clinical Research Associates). Must have previous experience in running clinical trials and posses strong analytical and statistical aptitude, with attention to detail and regulatory documentation. Must be able to work independently. Prefer mid level candidate.
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Medical Information Manager
(US-Massachusetts) Manages Medical Information Requests for company's marketed products. Train the Sales Representatives on Medical Information. Train company internal personnel on Medical Information. Provide Sales Force with copies of Medical Information responses. Receive and respond to medical information requests for marketed products that are received by client's 1-800 number, forwarded by outsourced contract research organization service groups, clients' Website, received by mail, or requested by the Medical Liaisons, the Sales Force or internal personnel. Audit the medical information database for tracking receipt and responses to medical information requests. Also, works with the administrative assistant to audit files. Receive and forward product or device issues to the Quality Assurance Department for follow-up. Perform literature searches for company's marketed products. Collate, summarize and disseminate pertinent literature to company internal personnel and field sales force.
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Senior Medical Writer
(US-Massachusetts) In this challenging and interesting position you will coordinate the execution of the strategic production plan that provides medical support to the post-marketing commercialization efforts of company's products. You will oversee day-to-day activities to insure that the publication plan is fully integrated with the commercialization plan. Working with the Development and Commercialization teams, the manager will be responsible for coordinating review of key publications and other public presentation materials relevant to the successful marketing of company's products and that they are in accord with the Publication Plan and key messages agreed to by the commercialization team to include abstracts, posters, manuscripts, reviews and slide kits. Using your exceptional medical writing skills you will prepare first drafts of abstracts and other support materials as needed for scientific meetings, create slide sets for each publication; ensure that appropriate SOPs are followed as well as track scientific meeting abstract submission deadlines.
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Group Director, Regulatory Affairs
(US-Massachusetts) Direct and manage the activities of RA Directors responsible for worldwide development projects. Develop corporate regulatory strategies and specific regulatory development plans for new product development. Implement strategies for rapid critical path development and approval of marketing application, including planning and strategy for IND development Ph 1-3, preparation and submission of new INDs, management of regulatory support activities for nonclinical development, support of clinical development , e.g. protocol reviews, development of product description template, draft product labeling, review of study reports, technical sections of NDA/CTD etc. Management of development and preparation of marketing applications (NDA and CTD electronic formats). Provide guidance and advice to senior management to achieve goals for regulatory timelines, strategy, nonclinical and clinical testing, development of product marketing promotional platforms and materials.
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Clinical Medical Services Information Analyst - B
(US-Illinois) Our client, a major pharmaceutical company in Waukegan, IL is looking for a Clinical Medical Services Information Analyst - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Provides lower level technical support to all Medical Services personnel with imaging and indexing documents, queries, and simple database construction. Provides all of the graphs, tables, and figures that allow for analysis and reporting of adverse experiences and quality issues. Coordinate internal department data for productivity reports. AS/BS Preferred. Job Title: Archive Data Manager Essential Functions and Responsibilities The Archive Data Manager is responsible for archiving clients' clinical study databases using the CDAS archiving software application. Specific responsibilities include 1) Identify studies ready to be archived from the archive catalog; 2) Generate archives using the CDAS application; 3) Review processing status of CDAS archive runs and verify that tasks run through to completion; 4) Review archive reports to identify any problems or issues.
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Career Coaching by Cindy: "What Kind of Car Are You?"
Go ahead, answer the question. If you were a car, what kind of car are you? Now, here’s the second part of that question. What does the car (that represents you) say about you to others? Classic? Macho outdoors type? A risk–taker? Or maybe, ho hum, average Joe? Next ask a friend what kind of car they believe you are? Go ahead. I’ll get to the point in just a moment. Finally, ask a business associate, your boss, or customer (or all three) the same question. Do the people with whom you interface see you as you see yourself? Chances are good they do not.
Click here for Cindy's complete article.
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