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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 Pharma R&d Inquiries

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Pharma R&d

Focus of the project: sourcing for the r&d wing of the big pharma which deals with the development of the methods to analyse, manufacture and test the drugs (process r&d). The project is an industry study to understand the sourcing mechanisms of the pharma industry for its process r&d wing. We intend to understand the sourcing models, process r&d organization structure, sourcing team structure and the performance management of these teams within the big pharma. The purpose of this study is not to solicit confidential information regarding companies but to gain insight into how large companies are structured and how they will change based on the future needs. The experts will be required to share their contact details to facilitate sharing of documents.

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    James |Managing Director

    I have worked on the supply side of th epharma industry for over 30 years responislbe for developing...

    7 Minutes Later
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    John |Chief Scientific Officer/VP-R&D, Technic

    I am interested in ***** this project. This is my area of expertise and experience and al...

    51 Minutes Later
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    Warren |Consultant

    Nidhyana, I would be interested in discussing this project with you....

    1.4 Hours Later
+29 Other Responses
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Bio Research Quality & Compliance (brqc)

Bio research quality & compliance (brqc) - pharmaceutical r&d services need expert with quantitative knowledge on supply market, market, pricing model, engagement model for quality assurance, quality analytics, quality management, quality management system oversight and quality planning & strategy of pharma r&d environment. Key deliverables: 1. Supply capability analysis - supplier’s functional capability/ competency, client base information 2. Sourcing best practices - outsourced vs. In-house trend, cost drivers/components, costing/pricing models, resourcing/ engagement models, quality kpis for supplier selection 3. Market trends - macro level knowledge on how suppliers tackle local regulations and its impact on brqc, macro level trends on technology, innovation - modeling, predictive analytics and its impact on risk management, technologies that can support training, audits etc.Quality vs. Cost perspective - low cost sourcing. Get in touch if you can help with all of above.

    +undefined 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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    Pharma R&d Strategy Project Opportunity

    Dear, i'm a management consultant with **** in india, a strategy consulting firm founded at stanford university. One of our core areas of expertise is pharmaceuticals and we have advised more than 80% of the top 20 global majors, and leading indian players on a host of strategic issues. We're currently in discussions with a mnc which is interested in scaling up their small r&d centre in india to develop products for emerging markets, which are currently being made in other locations in europe/ us. This would involve an assessment of the company's current development, manufacturing, regulatory, qc capabilities in india, assess what capabilities are needed to make the targeted products for the targeted markets, identify the gap, and where feasible help them scale-up the india centre to meet the requirements. In this context, i wanted to reach out to you to discuss if we could possibly work together. If this opportunity interests you, please reach me at the number below, or at this mail id at the earliest. Thanks, sidharth

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      D K |Consultant

      Hi! Mr. Sidharth, This sounds interesting and I think I might be able to help. Let me know how can...

      17 Minutes Later
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      Ronald |President Dadino Consulting, LLC

      I'm extremely interested in assisting you. I've done this type of project many times for many diffe...

      21 Minutes Later
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      George |Managing Member

      I have managed several companies for both research and development/manufacturing/clinical studies gr...

      27 Minutes 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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    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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    Eauctions And Strategic Sourcing

    Research background: the client wants to understand feasibility of sourcing via eauction of sub-services under preclinical (e.G. Drug metabolism and pharmacokinetics,pathology, toxicology, screening services,discovery chemistry etc. ) and clinical research (patient recruitment, clinical monitoring, site management, data management, biostatistics, drug safety) of pharmaceutical r&d. I am also looking for case studies illustrating how other top pharmaceutical companies are doing it and what are the intricacies and factors involved in arriving at the decision of sourcing via eauction. Qualification: looking for experts with prior experience in deploying eauction in preclinical and clinical research under pharma r&d

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      Jim |Principal

      Hello again, I have over 20 years experience with a ***** medical device and biotech/pharma...

      7.1 Hours Later
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      Vishal |Director

      I am interested to work on above proposal. Please free to ***** me any time....

      2 Days Later
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      Shaun |Senior Lecturer

      I have extensive experience in conducting clinical trials both in academia as well as in the industr...

      2.3 Days Later
    +5 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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