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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 Pharmaceutical Inquiries

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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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Drugs With Current/expired Patents

Looking for c-level responses from manufacturers of drugs with current and/or expired patents to take to china via established distribution network that handles sfda, regulatory/government relationships as well national, regional and local distribution channels.

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    Clifford |President

    Am interested in this opportity and have experience wiht *****ucts and those manufactured in...

    35 Minutes Later
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    Piet |owner / director

    Dear Sir, Sorry. You will have to find somebody else. I am not qualified for the project. Regards, P...

    1.7 Hours Later
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    LALIT |Freelancer Recruiter

    Dear Sir, I am Pharmacy and Clinical Research consultant. Please share your business model. Regard...

    3.8 Hours Later
+12 Other Responses
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Pharmaceutical Manufacturer

We are looking for experts at, or recently at, pharmaceutical manufacturers (major manufacturers preferred i.E., gsk, lilly, pfizer, etc.) for a <1 hour paid phone consultation. The questions i am trying to answer are: what is the specific value of increased prescription drug adherence to pharmaceutical manufacturers? How has biopharma been involved, or would they like to be involved, in the promotion or sale of devices that improve patient adherence? How does biopharma view the value of patient adherence data, what is that quantified value, and what is the current availability of that data? We would also be interested in experts from pharmacy benefit managers who can speak to the same issues of importance of adherence, involvement in increased adherence systems or devices, and importance/value of adherence data. We are looking to conduct at least 5 paid phone consultation this week for experts who are able to answer our research questions above. Please respond with your relevance to this request and a few availability windows for a call this week.

    +undefined 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 Distribution & Wholesale

    We are a new wholesale/distributor of non-controlled pharmaceuticals. We are in need of a policy and procedures manual for kentucky state inspection.

      +undefined Other Responses
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      Pharmacovigilance Business Development

      Job title: business development manager job location: open (us and uk) job type: full-time please note: this position is only open to u.S. And u.K residents seeking full-time employment. No consultants please. Position summary: will work collaboratively with other colleagues to increase sales within the life sciences industry. Responsibilities will include full cycle sales including; researching, identifying, cold/warm calling, getting client meetings, listening and understanding client needs, addressing client concerns/objections, proposing solutions, negotiating, obtaining sows and closing the deal. Are expected to quickly develop credibility with customers/prospects and build trust through professionalism and knowledge of our services and products. **essential duties and responsibilities**: - prospect accounts focusing on safety related to our products and services - identify and develop new accounts and following up on existing leads - develop and maintain positive and productive relationships with key target accounts - manage assigned accounts to generate both incremental and repeatable annual business - initiate and manage rfi and rfp process and negotiate terms for all account programs and projects - work collaboratively with the services organization to ensure a complete and professional delivery of our software and service solutions - collaborate with our executives and smes to maximize account coverage - maintain knowledgeable understanding of changing regulatory guidelines and mandates affecting the industry community **job experience and qualifications**: - must demonstrate a sustained (7+ years) and successful track record selling professional services to pharmaceutical, biotech, medical device, and/or clinical research organizations. - selling drug safety consulting services and products is desired. - candidates should exhibit an understanding of the regulatory pharmacovigilance process for both pre-marketed and post-marketed stages of a product. - experience working with regulatory affairs departments, product safety related departments, or regulatory submissions is highly desired. - experience with data-mining or statistical signal detection products is desirable. - demonstrated track record of success working with senior level management in a fast paced growth environment is essential. - full sales cycle experience is required (prospect, identify opportunities, propose solutions, negotiate, close). - strong, quality-oriented proposal writing and proposal management experience. - ambitious, driven and self-motivated personality is required. - college degree or equivalent experience required. - willing to travel throughout the us, estimated up to 80%. - background in software as a service (saas) market is preferred. **we offer**: - competitive base salary + commission. - benefits: 100% medical/dental for employee and his/her family. Interested applicants should reply with a brief summary of their relevant experience and attach their latest cv on zintro. Please note: this position is only open to u.S. And u.K residents seeking full-time employment. No consultants please.

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        Terry |Regional Sales Manager

        Please accept my resume for the Business Development Manager position. Thank you, Terry Brown...

        2.5 Hours Later
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        Alan |Consultant

        Thanks for reaching out. But altho' I have drug safety and reg submission experience , I have not w...

        4.2 Days Later
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        Ajay |

        yes, I can do this job....

        6 Days Later
      +49 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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      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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      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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      Pharma Research Interviewees

      We are seeking highest specialized experts with experience in the life sciences industry - must meet below specifications location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston. Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research. Testing availability: late june - early july study 1: qualitative study - focus group interviews with 3 groups (6-8 respondents per group) **respondent profile**: group 1: 6-8 pharmaceutical executives from top 20 biotech companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/clinical research organizations (cros). Group 2: 6-8 pharmaceutical executives from top 10 clinical research organizations (cros) companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations. Group 3: 6-8 pharmaceutical executives from small / mid-sized pharmaceutical companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations. **expert must have** a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others): a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management. E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc. F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.

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        Jukka |President, Director

        My experience covers all areas over 30 years. Have a look at my profile. I have recently consulted o...

        27 Minutes Later
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        Scott |Sr. Technical Services Project Engineer

        I am involved in most of the areas you need help with. I oversee all of our 3rd parties. Let me kno...

        45 Minutes Later
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        Kuldeepak |Director

        Thanks for your message. As a pharmaceutical consultant & Ph.D. in pharmaceutics, I have extensive h...

        53 Minutes Later
      +15 Other Responses
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      Pharma Qualitative Study

      We are seeking highly specialized experts with experience in the life sciences industry - must meet below specifications location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston. Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research. Testing availability: late june - early july study 2: qualitative study - one on one either telephonic or in-person interviews **respondent profile**: cost estimates for both tdi (telephonic interviews) and idi (in person interviews) with 8 respondents, 2 each from clinical trial supply managers/coordinators/directors, procurement contacts / outsourcing managers / directors, clinical / pre-clinical teams, senior executives (pharma/biotech/cro) **expert's job titles**: 1) clinical trial supply managers / coordinators / directors 2) procurement contacts / outsourcing managers / directors 3) clinical / pre-clinical teams 4) senior executives **experts must have a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others)**: a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management. E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc. F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.

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        Jukka |President, Director

        Can cover almost every area in detail. Been involved and leading development for 30 years. Would be ...

        29 Minutes Later
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        Scott |Sr. Technical Services Project Engineer

        I am involved in most of the areas you need help with. I oversee all of our 3rd parties. Let me kn...

        36 Minutes Later
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        Mohamed |Zintro Expert

        I am ***** Organe county area and happy to help with the project. Being global team lead for d...

        42 Minutes Later
      +18 Other Responses
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      Pharmaceutical Market Research

      We are looking for an expert who has strong knowledge in pharmaceutical real-time market research geography: global with much focus on us project overview: we would like to understand pharmaceutical real-time market research industry and partnerships that are working between suppliers. Deliverables that we are looking for: - suppliers who can provide real-time pharmaceutical market research - partnerships between traditional and real-time market research providers with advantages and disadvantages for buyers - sourcing models for real-time market research(through traditional research firms or boutique suppliers) with advantages and disadvantages thanks, balaji

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        Shyam |VP of Finance

        Hi Balaji, Have deep expertise and knowledgeable in Pharma real-time Market research and procurement...

        2.5 Hours Later
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        Ariovaldo |Finance Specialist, CFO and Controller

        Hi. I am based in Brazil. For any issue feel free to contact....

        2.5 Hours Later
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        Polina |Zintro Expert

        Hi Balaji, I support pharma MR with US focus, so I can respond to each of your questions. Email me ...

        3.2 Hours Later
      +9 Other Responses
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