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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.
  3. 3. You can communicate back and forth, qualify each other, connect and pay fees to Experts through Zintro.
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Recent Biotech Inquiries

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Biotech Patent Law

I am interested in a valuation of a biopharma patent(s). U.S. Patent application 20050085555. If you know anyone qualified that could tell me how the valuation process works, i would be appreciative. Charles

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    Margaret |Patent Agent

    Hello Charles, I can help you with that - it will depend on stage of the ***** the products (i...

    30 Minutes Later
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    Dale |Chief Scientific Officer

    Hello Charles. I might be able to help you but have a close colleague with many years experience who...

    4.2 Hours Later
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    Michal |Science and Technology Officer

    Dear Charles, I can definitely help you to ***** IP, as I am in the field of tech scouting, v...

    10.5 Hours Later
+5 Other Responses
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Biotech Startup

I am looking for a biomedical engineer/scientist with experience in developing medical technologies especially using nanotechnology. I need advice on various aspects of starting up a medtech/biotech company including financing, product development, technology transfer, business and strategic planning, and navigating the regulatory path.

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    Mark |Chairman & CEO

    I have extensive hands-on experience in pharma/medical *****uding GMP mfg, product develop...

    8 Minutes Later
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    Girish |President

    I think we have the expertise for what you are looking for and would be happy to discuss your projec...

    11 Minutes Later
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    R |CXO

    Regarding the ***** a technology startup, you may wish to take a look at the 'Mechanics ...

    20 Minutes Later
+25 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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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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Biotech Manufacturing Procedure

We need an expert witness in the field of biotech manufacturing procedures and or pharmaceutical manufacturing best practice. To advise court on issues relating to quality assurance and the failure to follow procedure (or not, as the case may be)

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    Klyushnichenko |VP, consultant

    Dear Colleague, I would be interested to help you with your project. Please reach to me to discuss ...

    8 Minutes Later
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    Barry |Principal, Barry Garfinkle & Associates

    I would be interested in your project. I was an executive at Merck for over 35 years. During that ...

    18 Minutes Later
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    daniel |director

    Please get in touch. Thank you....

    34 Minutes Later
+20 Other Responses
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Biotechnology Marketing

I am looking for somebody/consultor with specific knowledge in the pharma and biotech sector. The topic is launching a product for the reproductive female health. I expect that this person can contribute and support launching products, giving support to the marketing/sales department, pricing and competititors anlaysis. It is prefered experience in different countries emea and fluency in at least three european languages. Statistic analysis as well scientifical writing are desired.

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    Mary |President

    Dear Ms. Dreikorn, By way of introduction, my name is Mary Schwab. I am a biopharmaceutical commerc...

    18 Minutes Later
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    mohamed wagih |partner inegma resources

    IS English /ARABIC languages are accepted in this area EMEA...

    33 Minutes Later
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    Margita |CEO

    Dear Ms Dwakorn, I wanted to ask for some more *****rding the project. For when is the...

    1.4 Hours Later
+10 Other Responses
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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
+9 Other Responses
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Pharmaceutical Market Access

Director, market access opportunity onsite in california, usa. Overview: the director market access will be a strategic business leader responsible for developing a comprehensive reimbursement, pricing, contracting, and distribution strategy for heplisav-b in the us to support launch in 2016. In addition, the director market access will provide guidance and insights to support commercial planning for pipeline products. Responsibilities: build out the infrastructure for the pricing, contracting, distribution and payer team. Develop and execute market access strategies focused on reimbursement, pricing, contracting, and commercial distribution related to heplisav-b and future pipeline products across multiple disease states. Apply deep understanding of national and local reimbursement trends and policies, payer coding and billing, and newly forming health care delivery models to develop managed market strategies. Lead development and execution of contracting strategy for heplisav-b and future pipeline products. Lead all aspects of payer coverage to support appropriate reimbursement of heplisav-b. Develop dossier and other materials as needed to support payer acceptance. Responsible for all distributor and gpo accounts, including contract negotiations, ongoing relationship management, and day to day operational activities. Execute retail pharmacy channel distribution strategy in conjunction with product marketing. Manage 3pl activities related to interactions with distribution network. Work with commercial analytics to develop metrics/dashboards to assess performance of pricing and contracting strategy. Qualifications: at least 10 years of experience in the biotech or pharmaceutical industry; at least 5 years’ experience in a market access/reimbursement/key account position with proven success ba/bs with relevant experience; understanding of billing and coding with experience in the implementation of pricing and contracting strategy; comprehensive knowledge of us healthcare reimbursement system in both commercial and government payer; demonstrated experience with specialty pharmacy and wholesalers.

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    RAJNI |Managing Consultant

    Dear Manager 24 Sep 2015 I have vast experience in Infectious Diseases for ove...

    7.1 Hours Later
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    R. |Biotech Research Analyst/Scientist

    I can do this **********te in northern CA as required....

    11.4 Hours Later
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    Glenda |Principal Consultant

    As a pharmacist working on payer side for many years, I understand the issues surrounding market acc...

    17.8 Hours Later
+6 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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Zintro Webinars

We are hosting webinars presented by zintro experts as a way to source new clients for you. We promote the webinar invitation to our 180,000 users through email and other channels, then we post the webinar to our blog and promote the video. You can view some examples here. This initiative would be completely free for you. You would be able to include your zintro profile in the webinar to promote your services and you would only pay us 15% of any engagement generated through the webinar effort. Presentations are normally 40 minutes and focus on subjects that might showcase your expertise and help you source new clients. After your presentation, we will leave an additional 15 minutes of time to answer attendee questions live. To view some examples of past webinars, go to: https://blog.Zintro.Com/webinars/ i'm coordinating the schedule for the next available webinar slots and would like to know if you are available for any of the following dates: july 16th, 2015 1:00 pm edt july 30th, 2015 1:00 pm edt august 13th, 2015 2015 1:00 pm edt august 27th, 2015 2015 1:00 pm edt september 10th, 2015 2015 1:00 pm edt september 24th, 2015 1:00 pm edt october 8th, 2015 1:00 pm edt october 22nd, 2015 1:00 pm edt november 5th, 2015 1:00 pm edt november 19th, 2015 1:00 pm edt december 3rd, 2015 1:00 pm edt we usually hold a practice session on the monday preceding the presentation date. We can do the practice session at whatever time is most convenient for you. In addition to your preferred dates, i would appreciate if you could provide the following information: 1) zintro id or sign up email address 2) complete name and title 3) company you work for 4) topic of your presentation

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    Camille |Co-President, Managing Partner

    I am an industry-recognized expert in biotech and pharma and have spoken on the value of science id...

    31 Minutes Later
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    Larry |Presdient

    Happy to present a webinar for the cold supply chain sector ("The ***** the Last Mile in Cold Sup...

    1.4 Hours Later
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    Serge |President

    I am available for the August 13 or September 10 time slots Subject: Intercompany Design Control i...

    1.5 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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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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