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Recent Adverse Effect Inquiries

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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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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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Animal Health Pharmacovigilance Call Centre

Animal health pharmacovigilance call centre services - market , trends , insourcing vs outsourcing benefits , constraints and cost model, , supplier cost model

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    Alan |Consultant

    Interested by no vet PV exp...

    38 Minutes Later
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    Alex |Zintro Expert

    I am very much interested in this field and with 35 years of experriene in the veterinary field of w...

    47 Minutes Later
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    AMT |Drs., MSC DVM

    All about pharmacovigilance animal health? See my profile with special interst in pharmacovigilance ...

    52 Minutes Later
+14 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 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?

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    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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Pharmacovigilance

We are currently helping one of our clients - international cro with headquarters in germany - to build a team of freelance medical writers, clinical research associates, regulatory affairs and pharmacovigilance specialists for drugs and medical devices. They have indeed a large number of projects in the pipeline and need to strengthen the capacity of the in-house teams with extra support for the years coming.

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    German |Regional Research Director

    In ***** your recent post in Zintro, I'm pleased to introduce myself as an MD with close to 15...

    2.7 Hours Later
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    Steve |CEO

    Steve Jolley is a subject *****rt in all areas of global safety compliance and signal detectio...

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

    Hi Zi8b930f83! I will be glad to support your client. I am the MD & CEO of a global Pharmacovigilan...

    3.1 Hours Later
+42 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 seeking to hire for a pharmacovigilance (pv or phv) qppv position in the czech republic. Senior level, 10+ years of drug safety, pharmacological science experience. Collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. Here’s the basics for a qppv: contact responsible for ensuring company (the product's marketing authorization holder or mah) meets its legal obligations for the monitoring of the safety of a medicinal product on the market. The qppv must reside in the eu, and should be permanently and continuously at the disposal of the mah. Detailed information on the role and responsibilities of the qppv are specified in volume 9 of "the rules governing medicinal products in the european union."[2] at a minimum the qppv should be appropriately qualified, with documented experience in all aspects of pharmacovigilance in order to fulfil the responsibilities and tasks of the post. If the qppv is not medically qualified, access to a medically qualified person should be available.

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    Vivek |Associate Professor in Pharmacology & Cl

    Are you open to consider ***** this position?...

    1 Hour Later
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    Alan |Consultant

    I am based in USA. So I am not geographically qualified for this role....

    2.9 Hours Later
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    Graeme |Director of Pharmacovigilance. PharSafer

    Dear Sirs, I have served as an EU QP PV since 1995. However I am based in the UK. The role you descr...

    3 Hours Later
+12 Other Responses
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Cis Pharmacovigilance

Local pharmacovigilance contact person in cis countries and russia

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    Graeme |CEO, Business Development Director

    Dear *****, As a CRO - PharSafer - specialising in Global Pharmacovigilance we can certainly he...

    5 Minutes Later
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    Venkat |Owner

    sorry, I don't have any contacts in these countries....

    3.4 Hours Later
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    Vikram |Consultant

    Medical Doctor with 10years Experience in various pharma & Clinical research domains : clinical Oper...

    1.5 Days Later
+3 Other Responses
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Pharmacovigilance

We are looking for a suitable company/ freelancer with relevant pharmacovigilance. Expertise who would be able to take up local qppv responsibilities for italy. If interested, pls message me for further information.

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    Kristine |Zintro Expert

    Is this a remote opportunity? If so I would be interested in receiving additional information....

    2.8 Hours Later
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    Graeme |Director of Pharmacovigilance. PharSafer

    Dear Sirs, We are a global specialist Pharmacovigilance Company with many years EU experience and ca...

    2.8 Hours Later
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    AMT |Drs., MSC DVM

    Dear mr, mrs, please look at my profile on Linkedin, for human pharmacuetical companies I do have a ...

    2.9 Hours Later
+8 Other Responses
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Pharmacovigilance

Looking for an expert in pharmacovigilance italy

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    Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

    We have Pharmacovigilance experts in Italy. Please contact us....

    7 Minutes Later
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    santhoshkumar |QPPV

    Hi, Happy to share the Local PV ***** Italy ...

    8 Minutes Later
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    Babu |Pharmacovigilance & Regulatory Expert

    Hi, Please look in to my linkedin profile . in.linkedin.com/in/babuselvam/.. and get in touch me vi...

    8 Minutes Later
+4 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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