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Recent Clinical Toxicology Inquiries

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Liquid Chromatography Mass Spectrometry Brooklyn

Job title: lcms technologist growing clinical toxicology laboratory with an emphasis on drug testing that is seeking a ny licensed lc/ms technologist to join their team. Prior experience with toxicology drug testing required. Experience with lc/ms (liquid chromatography mass spectrometry) is a must. This full-time job post has been authorized by zintro. This position is not eligible for visa sponsorship.

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    Terry |Zintro Expert

    Thank you for you inquiry. Not a good fit. I am not licensed in New York or anywhere else, for tha...

    1 Hour Later
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    Dr. Paul |independent systems engineering/instrume

    I am fully qualified & expertly knowledgeable in the disciplines indicated. I would like very much t...

    2.9 Hours Later
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    Sabine |Zintro Expert

    I am not licensed....

    53.3 Days Later
+3 Other Responses
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Clinical Pharmaceutical Distribution And Logistics

We are looking for experts with strong understanding in clinical pharmaceutical distribution and logistics network. We want to understand competitive landscape (key service providers), cost drivers, pricing and sourcing models for clinical trials logistics with a focus on european region.

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    Vishal |Clinical Study/Project Manager

    Hi Piyush, have 8 years worth experience in various aspects of clinical trial conduct including oper...

    16 Minutes Later
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    Clare |Clinical Operations Consultant

    Hi Piyush, As you mentioned clinical trials in Europe I wonder if I might be able to help you? Pleas...

    14.2 Days Later
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    GARY |President

    please view ***** ***** consulting group (TBCG) online and contact me if you would like tor onto bi...

    39.2 Days Later
+3 Other Responses
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Pre-clinical Cro Market – Comparative Medicine

We are a global market research firm and are seeking experts who can assist us in understanding the ‘global pre-clinical cro market – comparative medicine’ key questions: 1. Kindly brief us on the key market trends related to comparative medicine (xenograft studies, lab animals and animal feed etc.) and toxicology studies 2. Which are the key innovations/advanced technologies offered by different vendors in the space of pre-clinical studies? A. What is the impact of digitization on the management of animal breeds? B. How the market is expected to evolve through 2025? 3. Which are the best practices adopted by leading pharmaceutical companies to build a category strategy in the space of comparative medicine and toxicology studies? 4. Kindly provide information around the current market scenario of pre-clinical studies including animal testing, in-vivo testing, pharmacokinetics and toxicology etc. 5. Which are the leading vendors in the global pre-clinical services market? A. Which is the preferred vendor segment for ease of animal sourcing? B. Kindly name top 10 vendors. What % market share do they occupy from the global pre-clinical services market? Which are their key capabilities? 6. Which are the different types of pricing models in the industry? A. Rate card vs module based pricing b. Most adopted pricing model currently 7. Information around animal supply chain (key focus on monkey supply) for pre-clinical studies. A. Are there any chances of animal supply shortage in the future? B. Which are the most preferred regions for animal sourcing and why? I. Is asia getting more preferred for animal (monkey) supply? C. Information on the animal supply market dynamics and how the global market place is evolving through 2025? 8. Case studies explaining best practices adopted by leading pharmaceutical companies to build a category strategy- a. How leading pharma companies are managing the category - comparative medicine and toxicology studies (in terms of supplier identification, and contracting)? B. Most adopted engagement models c. Most adopted pricing models d. How do the pharma companies streamline the process of managing the category and stakeholders? E. Cost reduction strategies we are looking for a phone consult for a period of 1 hour to discuss all points mentioned above.

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    Benita Saklani |Head Of Business Development

    Please suggest when you would like to schedule this discussion. Thank you Best regards, Benita Sakl...

    3.9 Hours Later
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    Karel |Chief Scientific Officer

    After having spent some 30+ years in *****linical results into human therapies I believe ...

    4.6 Hours Later
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    Panduranga |Senior Principal Scientist

    Glad to help...

    15.8 Hours Later
+24 Other Responses
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Clinical Development

Our client has an immediate need to conduct phone consults with multiple experts knowledgeable about best and worst practices for all capabilities of clinical development organization within pharma companies. More specifically, our client would like to better understand best practices revolving around structural organization and roles in these settings, as well as mechanisms for project collaboration, processes for clinical trials, forecasting, capacity management, governance and common pain points. Please note, this ask is specific to experience in the united states. Ideal candidates should have a deep knowledge of this space, and recent former experience at a large pharmaceutical company. Preferred expert will have recent (within the last 2-4 years) experience in a clinical development role at a large pharma company, speficially pfizer or merck. (client cannot speak to anyone currently employed by a pharmaceutical company). This project has a budget.

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    Jukka |President, Director

    I am very interested. I have my own consulting company (Pharma Consulting Services). Jukka ...

    35 Minutes Later
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    Larry |Presdient

    I have over 35 years experience in such areas and would be happy to speak with you. You can find us...

    36 Minutes Later
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    Scott |Sr. Technical Services Project Engineer

    I am a consultant in the pharmaceutical industry and have over 19 years experience in R&D, clinical ...

    39 Minutes Later
+35 Other Responses
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Workplace Exposure Limits Methodology Development

We are looking to work with consultants (preferably uk-based, but eu-based would also be considered) with experience covering both areas / subjects: - consultant with significant experience and a detailed track record of relevant work in relevant area (i.E. Work related to the methodology for developing workplace exposure limits). - senior toxicology specialist with academic qualifications, experience, professional reputation and detailed track record of their work in relevant area (i.E. Work related to studying the safety and effects of hazardous substances (in the air) on living organisms, as well as the general development of methods to determine harmful dosages, effects, and safe exposure limits). Project timeline: - project duration is 8 weeks, contract to commence 10th may 2021. Project deliverables: - research report; the format of the report is to be agreed. - provision of the service will include: a. Addressing the requirements and delivery of the outputs described. B. Meeting with client to finalize the scope of the work. C. Regular meetings with client to update on the progress of research report. If interested, please respond with: - brief summary of your relevant knowledge and experience in the space - proposed hourly rate - latest copy of your cv

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    Mohamad |Senior Researcher

    - (Jan 2021 - Present) Senior Research Scientist at the department of Infectious Diseases in San Pao...

    16.6 Hours Later
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    Lawrence |Director, Toxicology, Technical RA

    I have over 35 years professional experience in *****cology and health risk assessment in ...

    1.5 Days Later
+5 Other Responses
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Histopathology

Hello, histopathology services (animal and human analysis) we are looking for expertise in the market segments of histopathology services (animal and human analysis) specifically • sample preparation (e.G. Embedding/trimming/sectioning, staining and other technologies) • image analysis • pathology (including digital pathology) regards, harsh

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    Paula |President

    Hello, we have over 35 years experience in human and animal ***** also have digital ima...

    14 Minutes Later
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    Alix |Associate Director

    Hi, Have been ***** head. what is the purpose of the job? best. A...

    25 Minutes Later
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    Arkady |CEO

    Hello Harsh, I am working with Yale ***** to offer diagnostic services via digital *****...

    2.2 Hours Later
+14 Other Responses
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Toxicology Tests For Clinical And Forensic

We would like to speak with law enforcement officers who are knowledgeable and responsible for toxicology tests for law enforcement purposes and volume estimation in the us. They would like to better understand esoteric toxicology testing focusing on clinical and forensic testing used in driving under the influence of drugs (duid) and death investigation. This is a 60-min paid video interview for $200. If you are open to participating, please provide a brief answer to the questions below: 1. Do you order/select/conduct toxicology tests? Yes no 2. Are you involved in the selection of labs for outsourcing of toxicology tests? Yes no please note that we are only interested in your personal point of view and are not seeking confidential information. For every successful referral (client interviews referral) on this project, a $150 bonus is paid to the referrer.

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    Thomas |Program Director-Police Graduate Studies

    While I was responsible for drug testing at my agency, I am not that knowledgeable about the tests t...

    18.7 Hours Later
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    VICTOR |Zintro Expert

    Thanks for the solicitation. I am a medical doctor and ***** forensic ***** workp...

    8.8 Days Later
+2 Other Responses
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Director Of Clinical Operations

Director of clinical operations: (full-time, onsite position) as a key member of the management team, the director of clinical operations will oversee studies on our novel bioelectronic medicine platform, providing comprehensive clinical evidence to support marketing application submissions. Reporting to the chief medical officer, the individual will be expected to:  work closely with the medical, regulatory, quality, and r&d teams on the design of our clinical development program, and the plan for program execution  develop and manage operational plans for individual studies within the clinical development plan  author documents including clinical study protocols, investigator’s brochures and clinical study reports, and collaborate in the preparation of manuscripts and external presentations  manage clinical trials service providers and suppliers and interact closely with investigative sites,  develop sops and guidelines, and ensure compliance with regulatory agency requirements  recruit, hire, and manage additional clinical team members  lead, collaborate with, and mentor employees in other functional areas  qualifications:  the ideal director of clinical operations candidate will have:  10 years of experience in a fast-paced, demanding technical organization.  experience in clinical development of a class iii medical device is strongly preferred. Experience in the inflammation therapeutic area or closely related areas is a plus.  experience working with fda and other global regulatory agencies is preferred.  a bs or equivalent degree is required and a masters or doctoral level degree is preferred. Please attach your cv here to apply.

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    Tom |Chairman Emeritus

    Of course I would need more details, but I am interested in hearing more....

    1.4 Hours Later
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    Insynergy |Executive Director, Clinical Trials.

    I'm qualified by ***** experience for this position. I'm interested but need more informatio...

    6 Hours Later
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    Andrew |Director Business Development & Operatio

    January 28, 2016 Re: Director of Clinical ***** Dear Human Resources Director: Please allow...

    7.3 Hours Later
+13 Other Responses
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Clia Laboratory Operations

Need help to set up a toxicology lab in missouri. Need help in getting clia license also

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    Kenneth |Director

    Yes, I can undertake this project...

    1.3 Hours Later
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    Chris |Cheminformatics Consultant

    My company can help select, purchase, and set up ********** software for such a labor...

    1.4 Hours Later
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    Bob |Zintro Expert

    I am able to assist from equipment selection through CLIA ***** compliance. I have set up...

    3.1 Hours Later
+9 Other Responses
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Diabetes Research

Need someone to summarize the expected developments in diabetes in the next five years. Expected deliverable no more than a page or two. Most importantly on clinics, and clinic operators.

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    Kenneth |Senior Director

    I have been working in diabetic medicine for over 30 years and am familiar with drug and device dev...

    2.6 Hours Later
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    Srinivasan |Research Faculty

    Hi, I am a life science researcher. I can prepare this report. What is your time line and budget for...

    2.9 Hours Later
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    jennifer |Director of Marketing

    I have many years experience as a marketing professional in the diabetes *****....

    3.3 Hours Later
+33 Other Responses
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Ind Toxicology

Early phase nonclinical ind toxicology and clinical pharmacology small molecule drug regulatory pre-ind package

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    Kaela |Principal/Owner

    I have extensive experience (20+ years) in this area. Details can be found on my website: http://por...

    11 Minutes Later
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    Mark |President/Principal Consultant

    Folks, I am a board-certified toxicologist with much experience in IND toxicology studies/submissi...

    24 Minutes Later
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    Vijay |Consultant

    Yes, I have experience in pharmacology and toxicology and have submitted a number of INDs. How can I...

    1.4 Hours Later
+17 Other Responses
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Clinical Research

Looking for subject matter experts / consultants in clinical research, clinical trial, risk management, audit and inspection, gcp, clinical outsourcing, trial design and management,ethics fraud and misconduct, patient recruitment , documentation and management, clinical laboratories, facility/hospital , hospital clinical compliance, billing and coding for clinical services , patient/third-party coding and billing, sponsors, cros, clinical quality control/cqc for speaking engagements with over 25+ years of experience. Feel free to reach out to me.

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    Gabe |Clinical Trial Consultant

    I have experience in many of these areas www.g2crc.com...

    9 Minutes Later
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    Jeffrey |President and Managing Director

    I am an MD (certified in internal medicine)/PhD (basic pharmacology) with 30 years of pharmaceutical...

    10 Minutes Later
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    Victor |Director

    I have >20 yrs experience. Victorchen22 at *****...

    14 Minutes Later
+20 Other Responses
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