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  1. 1. Provide a clear description of your needs and your expectations of an expert, consultant or job candidate and Zintro will match it with the most relevant professionals in our platform.
  2. 2. Within a day or two typically 6 - 12 Experts, who have opted-in, will contact you with a brief explanation of their qualifications and how they can help.
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Recent Biotech Pharmaceuticals Medical Devices & Ivd Inquiries

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Online Medical Training

Hi all, i am looking for speakers/experts for online training in the below areas: medical device fda compliance pharmaceuticals biotech lab if you are interested, please leave your contact details and convenient time to connect. Best regards, rahul

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    Nicholas |Director R&D

    I have been in the medical device and pharmaceutical industries for over 40 years. Included many e...

    41 Minutes Later
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    Diane |Zintro Expert

    Dr. Diane Sudduth ***** (best time to contact after 4pm EST) Fluent in medical device quality...

    41 Minutes Later
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    David |Industrial support and development

    Hi, I have an extensive experience in medical devices (orthopedic and neurostimulation), both in va...

    42 Minutes Later
+30 Other Responses
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Pharmaceutical Development

I work at a human capital sourcing firm and am trying to find an expert or a consultant that can help me answer some questions about a potential investment. I am looking for someone who can help me better understand single-source providers of medical information, pharmacovigilance, and regulatory compliance concerning pharmaceutical development. If a candidate has international experience, experience in both pv and mi, experience in asia would be a huge plus, but not mandatory.

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    Aloysius |President

    BREEJ Technologies Consulting Group offers Consulting Services to the Pharmaceutical and Biotech Ind...

    2.7 Hours Later
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    Graeme |CEO, Business Development Director

    Dear Sirs, We are a specialist Global CRO focussing on Pharmacovigilance (Clinical & Post Marketing)...

    2.8 Hours Later
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    Jukka |President, Director

    I am able to help but need more details of the consultation....

    2.9 Hours Later
+27 Other Responses
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Pharmaceutical Engineering In China

Pharmaceutical doctor engineering. Nature of activity requested for experts (issues to solve, assignments, etc.) to resolve the technical problems like polymorph screening, crystallization process development, medical process r&d and engineering design and other fields in pharmaceutical manufacturing. Expert qualification (profession, degree, language, experience, etc.) time to start work, duration and working location 1, doctor in pharmaceutical engineering or related background; fluent in english more than 8 years working experience in multi-national enterprises acting as senior research scientist; and specialize in pharmaceutical process development, polymorph screening, process r&d and optimization or engineering. 2, time to start work: tbd 3. Duration: more 3 years with 9 consecutive months per year or short-term guidance tbd 4. Working location: zhejiang province; working conditions for experts (accommodation, allowance and other fringe benefits) preferential treatment and benefits; adequate research funding and professional team; salary tbd; number of experts required 4-6 proposed position executive pharmaceutical director

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    Timothy |Principal

    I am a former FDA Review Chemist, with > 30 years of career experience in pharmaceutical R&D, Qualit...

    1.7 Hours Later
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    Umberto |Previously: COO, VP & Director Regulator

    Dear inquirer, I have extensive experience in the pharmaceutical development and commercialization ...

    2.8 Hours Later
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    Terry |President

    I have more than 30 years of experience in both the pharmaceutical and diagnostic clinical trial ind...

    4.1 Hours Later
+7 Other Responses
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Life Sciences Online Training

We are a leading provider of educational webinars for the international life sciences community and we are looking for independent u.S.-based consultants/subject matter experts with a minimum of 10 years hands-on industry experience to provide interactive, online training for the pharmaceutical, biotech and/or medical device industry. Must have proven experience in instructional design and content development and be well versed in adult learning principles. This position may lead to a long-term contract.

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    Jukka |President, Director

    I may already be one of your experts - which company are you from?...

    1.6 Hours Later
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    Ali |DFSS MBB

    Let me know what you need. I train, coach, and mentor medical device functions in product developme...

    1.6 Hours Later
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    Evan |Independent Regional Sales Manager

    Contact me today because I can offer 25yrs of sales, sales training, sales leadership experience wit...

    1.7 Hours Later
+24 Other Responses
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Pharmaceutical And Medical Device Compliance

Our us firm is requesting individuals knowledgeable of either the fda or us dept. Of justice who are familiar with pharma industry and/or medical device industry compliance, including familiarity with the affordable care act (aca's) the physician payments sunshine act (ppsa) regarding disclosures of payments made to key opinion leaders by pharmaceutical and medical device companies. An ideal expert may be both (1) an attorney and (2) has experience defending or representing pharma or medical device companies on compliance issues? Secondly- i'm looking for someone from the usa who is a compliance specialist in either of the industries mentioned above (medical device and/or pharma) who is familiar with the "sunshine act" and has deep experience in helping these companies meet their disclosure requirements to the government. Referrals are also welcomed, thank you.

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    Pharma & Biotech Regulation And Compliance

    We are a small private equity fund looking for corporate attorneys from "white shoe" firms who have experience engaging with clients in the pharmaceutical and/or medical device industries regarding kol compliance (as regulated by the fda, oig, and/or us doj or similar entities in other countries). Have questions about trends concerning regulation of kol engagement, particularly with regard to "anti-kickback" legislation and the need for companies to monitor and track their kol engagements and payments in particular.

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      Clinical And Regulatory Medical Writing

      This is a full-time employment opportunity onsite in southborough, ma. **as a manager, clinical and regulatory medical writing you will: - implement project-specific strategies and assist with the development and implementation of department strategies to increase productivity and quality. - assist with the oversight of medical writing personnel. This includes hiring personnel, managing personnel matters, conducting performance evaluations, and training medical writing staff regarding applicable regulatory guidelines and medical writing practices. - assist with resource allocation and the development of business proposals related to the medical writing functions. - be responsible for the smooth functioning of all medical writing projects for clients and project teams through management of internal staff and the medical writing process. - serve as the lead medical writer on projects when appropriate. As the lead medical writer, you will draft and finalize documents necessary for all phases of clinical drug and device development, work with project managers to develop timelines and resource plans for the production of clinical documents, review statistical analysis plans and crfs, and perform peer and qc review of clinical study reports and clinical sections of regulatory submissions written by other medical writers. - and more! **required education and experience**: - bachelor’s degree or advanced degree, with some applied training relevant to the clinical trials or health research environment. - at least 5 years of medical writing experience in a cro, pharmaceutical, or biotechnology setting. Management experience preferred. - thorough knowledge of ich gcp guidelines and other applicable regulatory rules and guidelines and of medical terminology, clinical trials, and clinical research. - working knowledge of the relationship and regulatory obligation of the cro industry with pharmaceutical/biotech companies. - familiarity with moderately complex statistical methods that apply to phase i-iv clinical trials. **about our client** join a team that works on groundbreaking compounds and profoundly impacts patients’ lives! our client is a distinct, full-service contract research organization with offices in california, massachusetts, and quebec. They are serious about scientific integrity and has a dynamic company culture, including a focus on work-life balance. **value proposition for you** - flexible work schedule. - proven potential for professional growth. - a community of brilliant minds at your disposal. - the stability of working for a robust, financially sound cro that is growing at a sustainable pace. - exposure to more than 20 therapeutic areas, including cutting edge therapies such as immuno-oncology, biosimilars, gene therapy, and new molecular entities. Note: please attach your latest cv along with your response on zintro.

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        Ivan |Zintro Expert

        November 9, 2015 Dear Sir / Madam I am very interested in the position of Manager, Clinical and Re...

        6.1 Days Later
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        Gayatri |Zintro Expert

        I am interested...

        14.6 Days Later
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        New |

        Dear Hiring Manager, I am submitting my resume for ***** the position of clinical and ...

        21 Days Later
      +18 Other Responses
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      Vice President, Biometrics

      Join a team that works on groundbreaking compounds and profoundly impacts patients’ lives! our client is a distinct, full-service contract research organization with offices in california, massachusetts, and quebec. Due to their growth and investment they have recently relocated our headquarters to southborough, ma. They are serious about scientific integrity and have a dynamic company culture, including a focus on work-life balance. Value proposition for you: * flexible work schedule. * proven potential for professional growth. * a community of brilliant minds at your disposal. * the stability of working for a robust, financially sound cro that is growing at a sustainable pace. * exposure to more than 20 therapeutic areas, including cutting edge therapies such as immuno-oncology, biosimilars, gene therapy, and new molecular entities. As the vice president, biometrics you will… * be a critical part of the global core leadership team by being responsible for the guidance and strategic direction of the global biostatistic and data management teams. * advance the overall success and future growth of our client by having executive contact with current clients, providing key client oversight and strategic project contribution, and contributing to new business development. * develop and implement department strategies to increase productivity and quality, while decreasing cycle times and costs. Oversee the data management and statistical aspects of client projects and project teams. * participate in presentations of capabilities and research proposals to prospective clients. Represent data management and biostatistics in marketing efforts by developing project bid proposals, participating at bid defense meetings, or performing client presentations. * provide oversight of the hiring and management of personnel. Ensure that adequate training occurs and that performance evaluations are completed. * and much more! education: degree in statistics, biostatistics, math, or a related field. Phd or master’s degree preferred. Experience: * at least 15 years of relevant work experience and at least 5 years of supervisory experience. * experience in a leadership position within biostatistics or data management for a cro. * have previously contributed to the overall strategic direction of a company or business unit. * thorough knowledge of ich gcp guidelines and other applicable regulatory rules and guidelines and of medical terminology, clinical trials, and clinical research. * working knowledge of the relationship and regulatory obligation of the cro industry with pharmaceutical/biotech companies.

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        Guillermo |Software Developer

        Let me know if you need an expert in Scientific Computing and Scientific *****times we...

        59 Minutes Later
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        Serge |President

        I am the former Manager, *****tegy at Bio-Rad *****, where I was responsible for t...

        1 Hour Later
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        Jean |President-Consultant

        Hello, I have been involved as manager of clinical *****gement and biometrics for 25 years, mai...

        22.4 Hours Later
      +27 Other Responses
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      Active Pharmaceutical Ingredients

      I am looking for experts who can help me in understanding advances / trends in api manufacturing technologies. Please find below the list of questions for which i am looking for your support. 1. What are the various api manufacturing methods and what are the new technologies in each manufacturing method and what are the adoption rates? 2. Please provide the technology evolution of api manufacturing process 3. What are the upcoming technologies in manufacturing that can be applied to all types of apis 4. What are the technology trends or upcoming technologies with respect to the manufacturing following types of apis and what are their adoption rates? Please provide the examples of few companies that have adopted those new technologies: • synthetic apis • biotech apis that includes monoclonal antibodies and recombinant proteins • hpapis – (highly potent active pharmaceutical ingredients) 5. Please provide technology trends, their adoption rates with respect to and their applicability to all types of apis: for example, if there is a new technology in solvent recovery, will it be applicable for all types of apis such as small molecule apis, synthetic apis and all other types. • small molecule manufacturing, • microbial and mammalian protein expression, • monoclonal antibody production, • advanced process controls, • solvent recovery, • effluent treatment, • continuous processing, • particle engineering, • downstream product recovery processing (filtration, sedimentation, centrifugation, extraction, precipitation, adsorption, membrane separation, chromatography, crystallization, and drying), • process analytical methodology,

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        Larry |Presdient

        Happy to help you with this. I have over 35 years experience in this area. You can find me at nexgen...

        7 Hours Later
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        Richard |Consultant

        Dear Inquirer: I am a professional with more than 10 years of experience in Life Science product de...

        9.1 Hours Later
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        Lajos |PhD

        To Whom itmay concern The list of questions and *****ghts are too general to repond, however ...

        15.2 Hours Later
      +12 Other Responses
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      Pharmaceutical Industry

      Hi zintro expert,the zintro blog needs you! we are looking for expert opinions on the news mentioned below and would like to include your point of view.  we realize your time is valuable, so here is a brief summary of what we are looking for: *a brief answer to the prompt about 1-2 paragraphs including your full name*participation is voluntary no payment will be involved*if chosen, you will be named in the post and we'll include a link to your zintro profile which will generate more visitors for you topic and prompt teva pharmaceutical industries ltd. And active biotech ab said monday they were ending the higher-dose portions of two multiple-sclerosis studies with the drug laquinimod after eight patients suffered nonfatal cardiovascular events.The companies said the incidents occurred in the higher-dose components of a phase 3 and a phase 2 clinical trial. The lower-dose and placebo components of the tests will continue.Phase 3 clinical trials are typically the last phase before a drug gets approval from the u.S. Food and drug administration.Teva shares fell 1.3% in early trading in new york, and active biotech shares fell by about one-third in stockholm.Laquinimod is a once-daily oral drug being developed for treating multiple sclerosis and huntington disease. What are your thoughts? Getting your name and expert opinion published on our blog is a great marketing opportunity. if interested, please send a response to the prompt via znotes within 1-2 days.Don't forget to include your full name.If you have any questions, please let us know.Thank you! the zintro blog team wondering what the post would look like? Here is a sample: http://blog.Zintro.Com/2014/08/14/rosetta-completes-10-year-trip-deep-space/>

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        Balkrishna |Zintro Expert

        My linkedin profile can be viewed to get details about my background in industry.You can contact me ...

        6.2 Hours Later
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        Polina |Zintro Expert

        I am interested in contributing. Please let me know what it involves....

        7.2 Hours Later
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        Jacob |President/CEO

        The incidents described are typical when testing a drug in the advanced stages of phase 2 and 3. at ...

        17.6 Hours Later
      +7 Other Responses
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      Market Access And Reimbursement

      We are looking to connect with directors and sr. Managers within market access/reimbursement from the top 100 pharmaceutical, biotech, and medical devices companies in the us (and potentially canada), to conduct a 20 minute online survey. If a good fit, we will compensate each person $100-175 for the 20 minute web survey. Topic: understanding the process of how companies get new products onto a payer's formulary

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        Biotech, Pharmaceuticals Marketing

        We are a pharmaceutical company in litigation as a co-promotion partner because the brand owner developed financial problems and refused to pay the co-promotion fees. The brand company is now claiming that we, the co-promotion company, did not preform to industry standards as their primary defense. We need an expert witness to verify that we did in fact preform to industry standards as far as calls, sampling and marketing.

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          Joanne |CEO

          I would be happy to help u with this project....

          3 Minutes Later
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          Joan |"On Demand" Consultant

          Please see my profile on LinkedIn to see if my academic and consulting ***** Marketing a...

          9 Minutes Later
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          Rita |Principle

          Dear Biotb8g2aW, I would be very happy to assist you with this project. I have been in several situ...

          3.6 Hours Later
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