Source Pharmacology Experts for your Project, Phone Consult or Job

Submit an anonymous Inquiry -- Start receiving responses within a few hours

Have a need? Explain it here

Zintro does not display, sell or trade e-mail addresses

An eye iconForgot password?
Submit Inquiry

By clicking Submit Inquiry you agree to our TermsVIEW

or Request Pricing Information

How Zintro Works

  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.
  4. Zintro is free, anonymous and without obligation.

Loved by Thousands

Loved by thousands logos

Need Help?A phone icon1-877-236-7016

Recent Pharmacology Inquiries

Area Icon

Pharmacology

Senior scientist/associate director – pharmacology, this an employment opportunity in california, usa. Responsibilities this new role will interact with senior management and serve as the company-wide resource in the areas of pharmacokinetics and bioanalysis. The successful candidate will: -participate in the design, implementation, analysis and reporting of preclinical studies generating pk or pk/pd data -conduct modeling/simulation of pk and pk/pd data which seek to predict human efficacious dose, optimize dosing regimen, describe exposure-response and model probody activity -provide pk(/pd) guidance in development of nonclinical and clinical study protocols -select and manage outside labs providing contract pk or bioanalytical services -oversee method development/validation and innovate as necessary to meet program needs for probody or pdc bioanalysis -work closely with project scientists, toxicologists, clinical leads and multi-disciplinary teams to develop an integrated approach to probody bioanalysis and pk assessment -contribute to the writing of study reports and organization of pk data in support of regulatory submissions requirements: -phd, or pharm.D. In pharmaceutical sciences or a related field -7+ years relevant industry experience supporting both preclinical activities and clinical trials; experience must include therapeutic antibodies and/or antibody-drug conjugates -proven proficiency in the use of pk and pk/pd data analysis software, compartmental & non-compartmental data analysis as well as modeling and simulation. -state-of-the-art knowledge of large molecule bioanalysis including pk, pd and ada assays for antibodies and adcs -the candidate should have extensive experience in working with multidisciplinary teams, competency in developing strategy and guiding pk-based drug discovery/development decisions

  1. Profile Picture

    Endre |CEO, CSO

    Dear Sir (Madam), I am interested in this position. I have beed the head of pharmacology at Sanofi ...

    18.7 Hours Later
  2. Profile Picture

    Steven |Zintro Expert

    Dear Human Resources, I am quite interested in the available Senior Scientist / *****ctor,...

    5 Days Later
  3. Profile Picture

    Anthony |Zintro Expert

    Yes, I wish to apply for this position of Senior Scientist/Assoc Dir Pharmacology ...

    11.8 Days Later
+9 Other Responses
Area Icon

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

  1. Profile Picture

    Michael |Principal Consultant

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

    4.3 Hours Later
  2. Profile Picture

    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
  3. Profile Picture

    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
Area Icon

Pharmacology

I'm looking for a pharmacologist to interpret a rat pharmacology study report of an anti-inflammatory drug.

  1. Profile Picture

    Bruce |Consultant Pediatrician

    My experience with *****udes being physician for first-in-human studies of PDE in...

    12 Minutes Later
  2. Profile Picture

    SURESH KUMAR |CLINICAL PROJECT MANAGER

    Let me know more details...I can help you....

    33 Minutes Later
  3. Profile Picture

    Chad |Consultant

    Hi - my name is Chad Beyer and I have a PhD in Neuropharmacology. I have worked with pharmacologica...

    3.5 Hours Later
+15 Other Responses
Area Icon

Clinical Pharmacology Sourcing

I am looking for an expert who can help us understand the following: 1. What is industry best in class partnership model for clinical pharmacology (phase 1 through phase 2a)? A. What is they typical mix of suppliers (clinical pharmacology service providers, cros and niche suppliers) involved by the major pharmaceutical companies? B. How do pharmaceutical companies leverage their internal clinical pharmacology units? Do other companies maintain and grow these units, or sell them off and outsource the activity? 2. Which companies are leveraging best their early phase and late phase cro activity. Which suppliers are they using? What benefits are they achieving by leveraging and ep and lp activity with the same cros? 3. As the partnerships with pharmacology suppliers or cros typically goes on for 3 to 5 years, gsk would like to understand how ep clinical pharmacology is expected to grow or change in the next 3 to 5 years. 4. Who are the leading suppliers including cros for clinical pharmacology? 5. What is the benefit of engaging with cros directly versus subcontracting through existing suppliers? Does this bring a significant change in margins charged by the suppliers? Thanks.

    +undefined Other Responses
    Area Icon

    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.

    1. Profile Picture

      Terry |Regional Sales Manager

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

      2.5 Hours Later
    2. Profile Picture

      Alan |Consultant

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

      4.2 Days Later
    3. Profile Picture

      Ajay |

      yes, I can do this job....

      6 Days Later
    +49 Other Responses
    Area Icon

    Pharmacovigilance

    Looking for an expert in pharmacovigilance italy

    1. Profile Picture

      Vijay Venkatraman |Managing Director & CEO, Oviya MedSafe

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

      7 Minutes Later
    2. Profile Picture

      santhoshkumar |QPPV

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

      8 Minutes Later
    3. Profile Picture

      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
    Area Icon

    Clinical Pharmacology

    All mandates )in china) associated with the requirement of in country clinical pharmacology studies and other information related to the same

    1. Profile Picture

      Vijay |Consultant

      Not clear as to what is the issue. I am currently the Director of Clinical Research managing about 2...

      2.5 Hours Later
    2. Profile Picture

      Donald |Director

      Sorry-not familiar with this subject...

      2.8 Hours Later
    3. Profile Picture

      Shakil |Chief Scientific Officer

      Not sure what is needed. I am CSO with a CRO and conduct all PK?TK analysis for in-house and outside...

      3.9 Hours Later
    +10 Other Responses
    Area Icon

    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.

    1. Profile Picture

      Kristine |Zintro Expert

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

      2.8 Hours Later
    2. Profile Picture

      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
    3. Profile Picture

      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
    Area Icon

    Local Pharmacovigilance -italy

    Looking for a pharmacovigilance local qppv in italy

    1. Profile Picture

      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
    2. Profile Picture

      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
    3. Profile Picture

      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
    Area Icon

    Pharmacology

    We are looking for an expert in pharmacology to act as an expert witness, to provide a report, and potentially give testimony at a civil trial. We represent the plaintiff in a civil lawsuit. Defendant's expert has opined that a prescription drug, which exhibits an affinity for dopamine receptors, may have led our client to become "hypersexualized." we are looking for an expert to rebut this particular report, after conducting relevant research. Please respond with your relevance to this request.

      +undefined Other Responses
      Area Icon

      Pharmacology & Toxicology

      My wife is claiming damages against the hospital staff as she was given a lidocaine infusion which the hospital have admitted was not the right does know has ptsd and other disorders we are looking for help as the lawyers say without expert witness in pharmacology we will only get a little amount we have other witnesses who say this is right but we need expert witness who will say it was the lidocaine what did this. Note from lawyers - a pharmacologists who were willing to provide us with an opinion for your selection. As discussed at our meeting with tim hammond on 11 october 2011, happy to pay once court case has been won which we will just on how much they value my wifes life as she cant work anymore 20 years left of her life and they are only offering 300k at the moment we have stated we want over $2 million for the rest of her life please help

      1. Profile Picture

        Esam |President, Adjunct Professor of Medicine

        I will be pleased to consider working on the case. However, I need to be be retained by an attorney...

        11 Minutes Later
      2. Profile Picture

        Michael |Director

        Are you still seeking an expert witness on this case?...

        6.1 Hours Later
      3. Profile Picture

        Avinash |Phameceutical Medicine Expert

        Dear Jonathan, This is the case of the adverse drug reactions to your wife with the lidocaine overdo...

        1.7 Days Later
      +10 Other Responses
      Area Icon

      Pharmacovigilance

      Looking for drug safety and pv folks in the following areas for the us: business development, consulting services, validation and project management. These are full-time and right to hire roles with an awesome and growing company

      1. Profile Picture

        Jukka |President, Director

        Dear Sir, I am MD, PhD, Board certified in Pharmaceutical Medicine, ***** General Medicine,...

        1.2 Hours Later
      2. Profile Picture

        Joseph |Pharmaceutical Consultant

        I am a former head of Drug Safety (Pharmacological) in the pharmaceutical industry and currently per...

        1.5 Hours Later
      3. Profile Picture

        Alan |Consultant

        I have abt several yes large pharma exp in pharmacovigilance : *****rts, Safety Updates an...

        1.7 Hours Later
      +26 Other Responses
      See More Inquiries

      Top Pharmacology Experts

      See More Experts
      Share
      LinkedInTwitterFacebookGoogle+