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Recent Adverse Effect Inquiries

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Pharmacovigilance And Medical Writing

Is the cost effectiveness and offshore landscape of pharmacovigilance and medical writing changing from india to other low cost countries such as china and philippines or other regions such as eastern europe and latin america? Are there any areas of opportunities in this space?

  1. Profile Picture

    Thomas |Principal-member, Owner

    You only need to research why the activities you mentioned were first identified as being able to be...

    1.6 Hours Later
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    Steve |CEO

    Please contact me if you would like to discuss this further. I have worked with a number of contract...

    13.3 Hours Later
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    Dnyaneshwar |Experienced pharmacovigilance /clinical

    Dear Manish, I am ready to help you....

    17 Hours Later
+6 Other Responses
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Local Pharmacovigilance -italy

Looking for a pharmacovigilance local qppv in italy

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    Graeme |Director of Pharmacovigilance. PharSafer

    Dear Sirs, We can help in this respect having local QPs and knowledge of the EU safety reporting, so...

    5 Minutes Later
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    Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

    Hello! We can support this requirement as we have EU QPPVs and Italy Local QPPVs on our panel. Pleas...

    33 Minutes Later
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    AMT |Drs., MSC DVM

    Hello i am interested and experienced both human and veterinary. Please forward my details for a tel...

    4.2 Hours Later
+4 Other Responses
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Pharmacovigilance

We are international company situated in prague, czech republic, which offers diversity of services, such as pharmacovigilance, regulatory affairs, medical writing and other services to life science companies.We are looking for a company or pharmacovigilance specialist for a literature screening for fiji, new guinea and solomon islands.

    +undefined Other Responses
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    Pharmacovigilance

    Pharmacovigilance department structure in top global pharma companies. Organization structure staff strength job roles and responsibilities

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      Irina |Therapeutist, medical director

      i am pharmacologist and clinical pharmacologist...

      10 Minutes Later
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      Samia |manager

      Hello, I have already developed pharmacovigilance department, please contact me for more details. M...

      24 Minutes Later
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      Raquel |R+D Quality Assurance Auditor

      Dear User, Is it possible to have your e-mail? Your questions require a wide response and I'm not su...

      34 Minutes Later
    +14 Other Responses
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    Pharmacovigilance And Medical Information

    We're looking for someone to consult about pharmacovigilance and medical information. We’re looking for someone with recent experience as chief medical officers, vice presidents of pharmacovigilance, or vice presidents of medical information/communications, and with experience in outsourcing these services. Please send me a message with what you can discuss and i'll answer as soon as i can. Sofía.

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      Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

      Hello! I am the Managing Director & CEO of a Pharmacovigilance consulting & Drug Safety services com...

      43 Minutes Later
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      Vicki |QPPV and Pharmacovigilance Consultant

      Hi Sofia, I have worked at a senior leadership level within Pharmacovigilance, with responsibilities...

      43 Minutes Later
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      AMT |Drs., MSC DVM

      Dear mrs, I was a QPPV for many years within the EU. Now pharmaceutical companies outsource there ex...

      46 Minutes Later
    +15 Other Responses
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    France Pharmacovigilance

    Dear, i would like to ask you, if you are interested to be a local pv person in france. We wish to submit a dcp in march 2015 for ibuprofen and paracetamol combination tablet . In accordance to article 104(4) of directive 2001/83/ec we require a contact person for pharmacovigilance issues at a national level for. This local pharmacovigilance contact will report to the qualified person responsible for pharmacovigilance activities. Can you please provide me with the price estimation for the above-mentioned activities? Thank you in advance. Best regards, maciej

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      Michael |Principal Consultant

      Dear Maciej Our company can offer the services of the local pharmacovigilance person in France under...

      4.3 Hours Later
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      Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

      Dear Maciej, Our ***** Local QPPVs (LRPs) in France and we can offer cost-effective serv...

      4.4 Hours Later
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      AMT |Drs., MSC DVM

      Dear friend, I would like to participate. I have to find out if I do comply with the *****ir...

      4.4 Hours Later
    +10 Other Responses
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    Pharmacovigilance

    Looking for global qppv psur and pv/drug safety consultant for an ongoing project in basel, switzerland. This is a backfill for someone who is leaving in december so immediate availability is necessary. Message me for more details? Thx!

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      Vivek |Associate Professor in Pharmacology & Cl

      Would you be interested in a perfect academic and experienced background? If yes, pleaee contact me....

      30 Minutes Later
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      Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

      If you are interested in outsourcing/contracting this activity to my organization, we would be happy...

      40 Minutes Later
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      Richard |Medical Director

      SUMMARY OF ***** An MD/PhD with over 10 years experience of clinical research and drug saf...

      45 Minutes Later
    +27 Other Responses
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    Animal Health Pharmacovigilance

    Animal health pharmacovigilance - looking for expert who could give details regarding the cost model(cost components),pricing models followed , offshoring/outsourcing strategies, contract models available for animal health pharmacovigilance - global scope with regional focus

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      Goran |Owner

      Generally the cot model of outsourcing expert is to pay him per hourly ***** by quoting him for t...

      1.5 Hours Later
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      Girish |Principal Scientist

      Please contact me if you are interested. Dr. Girish Please have a look in my LinkedIn profile (Dr. B...

      16.4 Hours Later
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      Timothy |Director of Research SCARF

      We have staff with experience in pharmacovigilance management for several pharmaceutical countries. ...

      1.5 Days Later
    +11 Other Responses
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    Pharmacovigilance

    We need a pharmacovigilance (pv) expert for a phone consult who has significant experience designing pv audit programs for internal processes, external facilities, vendors and partners in alignment with good pharmacovigilance practice (gvp)

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      Steve |CEO

      Steve Jolley has worked in the pharmaceutical industry since 1985 in the areas of clinical developme...

      1.7 Hours Later
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      Kuldeepak |Director

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

      1.8 Hours Later
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      Polina |Zintro Expert

      I have PV experience and PV audit program design. Please share with me your agenda at *****...

      1.8 Hours Later
    +16 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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    Pharmacovigilance Auditing

    I am looking for pv auditor located in egypt and lebanon for pv audit that will happen in q4 2016.

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      Steve |CEO

      I have conducted over 100 PV audits and would be happy to help you with this....

      3.6 Hours Later
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      Jose Alberto |Pharmacovigilance consultant

      We are not ***** Egypt and Lebanon, but can do PV audits. PVpharm. Please contact us with more ...

      3.7 Hours Later
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      Christopher |Principal Consultant

      We can assist you with your PV audits....

      3.8 Hours Later
    +11 Other Responses
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    Pharmacovigilance

    Pharmacovigilance drug safety

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      Krishna |Principal

      Can you provide any other details?...

      14 Minutes Later
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      Jose Alberto |Pharmacovigilance consultant

      Do you consider someone working from the EU?...

      46 Minutes Later
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      Raj |Associate Director

      Hi , thanks for the inquiry. Please let me know the ***** India and what kind of help is neede...

      55 Minutes Later
    +33 Other Responses
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