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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 Cro Inquiries

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Clinical Research Organization

Hello, we are a prominent nyc-based expert network and an authorized zintro partner our client has an immediate need to conduct phone consults with multiple experts knowledgeable about contract / clinical research organization (cro) industry. More specifically, they are hoping to better understand the overall market growth, trends & outlook, as well as key segments. Here's more information on the type of people they are looking to speak with: • a cross-section of pharma and biotech players of different sizes o expert must have ownership of development pipeline o have expertise related to key large/growing tas (therapeutic areas) and regions – initial hypothesis is focused on oncology, infectious diseases/vaccines, immunology o we would probably like to speak to mostly us players, some european and a couple in asia • sponsor members who own (or influence) outsourcing decisions (e.G., operations, clinical research) • cro members responsible for strategy/planning and pricing decisions • potentially across other segments of the value chain thanks, tj

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    Hong |Expert Physician

    Over 20 years extensive *****ical and pre-clinical experience, strong global clinical t...

    52 Minutes Later
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    Laura |MD -Clinical Research Professional - Fre

    Hi, I would be glad to help. I am a senior clinical research consultant, based in Argentina, providi...

    53 Minutes Later
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    Kuldeepak |Director

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

    1.5 Hours Later
+19 Other Responses
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Business Development For Contract/clinical Research Organisation

Looking for an expert to help in business development strategies and tactics for a niche cro (contract/clinical research organisation), specifically as it relates to exploiting scientific expertise and connecting to scientific decision makers in pharma and biotech

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    Vijay |Clinical Project Manager

    Hi there, I would be able to help. Please send further details. Kind regards, Vijay Zala...

    13 Minutes Later
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    Pieter |Owner of ClinTrimag

    I might be able to help, especially with Imaging CRO BD work. Expertise in MSK, Neuroscience and Onc...

    27 Minutes Later
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    Theresa |Industry Consultant for Clinical and Bio

    Hi. I have held Director of BD positions in 2 CROs. It is a tough market to enter but still possi...

    38 Minutes Later
+18 Other Responses
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Pharma Qualitative Study

We are seeking highly specialized experts with experience in the life sciences industry - must meet below specifications location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston. Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research. Testing availability: late june - early july study 2: qualitative study - one on one either telephonic or in-person interviews **respondent profile**: cost estimates for both tdi (telephonic interviews) and idi (in person interviews) with 8 respondents, 2 each from clinical trial supply managers/coordinators/directors, procurement contacts / outsourcing managers / directors, clinical / pre-clinical teams, senior executives (pharma/biotech/cro) **expert's job titles**: 1) clinical trial supply managers / coordinators / directors 2) procurement contacts / outsourcing managers / directors 3) clinical / pre-clinical teams 4) senior executives **experts must have a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others)**: a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management. E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc. F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.

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    Jukka |President, Director

    Can cover almost every area in detail. Been involved and leading development for 30 years. Would be ...

    29 Minutes Later
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    Scott |Sr. Technical Services Project Engineer

    I am involved in most of the areas you need help with. I oversee all of our 3rd parties. Let me kn...

    36 Minutes Later
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    Mohamed |Zintro Expert

    I am ***** Organe county area and happy to help with the project. Being global team lead for d...

    42 Minutes Later
+18 Other Responses
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Fte In Pharmaceutical Industry

I would like to know pharmaceutical industry average number of ftes/resources in-house who conduct 15-20 clinical studies annually, outsources clinical trials to cros(contract research organizations) and has an internal team who can validate the data generated by cros. Thank you

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    Liqiang |Associate Director

    I am the head of biometrics in an oncology drug company. I can provide the ***** need....

    5.9 Hours Later
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    Matthew |CSO and Chairman

    Depends on: Protocol Indication SOW (scope of work) Need of ***** sponsor Projections bas...

    6 Hours Later
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    Szabolcs |Clinical Research Director

    Ia...

    6.1 Hours Later
+35 Other Responses
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Clinical Research Organization (cro)

**please respond to the following request with a proposal if: 1) you currently, or within the last year, work at a pharmaceutical or biotech firm. 2) you are familiar with phase 1 clinical trials. Familiarity with and understanding of how biopharma and pharmaceutical companies decide which cros to use for early stage phase 1 clinical research. Will be able to speak to growth trends related to spending on r&d in industry and spending on cro services. To the extent possible, will be able to speak to how this may differ for innovator versus generic drugs. Will be able to speak to the reputations of different cro service providers for early stage phase 1. 1) how has your spending on cro early stage services trended in the past few years? What is your outlook for demand for cro services? Why? To the extent you can speak to this, how has this differed for generic vs. Innovator drugs? 2) what is the decision process for determining which early stage phase 1 cro to use? 3) what factors are considered when determining which early stage phase 1 cro to use? 4) what are the early stage phase 1 cros that come to mind? Which cros have you considered? How do cro reputations differ across the different stages of clinical research (early vs. Late)? For different clinical services? 5) what are the trends for early stage phase 1 cro services moving overseas? Areas of expertise: seeking experts with knowledge of clinical trials, phase 1-4; clinical trials; early clinical research; cro; early stage clinical research; cros; clinical research organization; clinical research

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    Insynergy |Executive Director, Clinical Trials.

    Hi, I'm expert in Phase I clinical research, I received this request many times. I'm so sorry that I...

    3.5 Hours Later
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    Rishit |Executive

    How can I help you? Dr. Rishit...

    16.8 Days Later
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    Jill |Director Project Management, Director Bu

    I sent your question to an ***** may be able to help you. Best regards, Jill...

    19.8 Days Later
+7 Other Responses
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Vice President, Biometrics

Join a team that works on groundbreaking compounds and profoundly impacts patients’ lives! our client is a distinct, full-service contract research organization with offices in california, massachusetts, and quebec. Due to their growth and investment they have recently relocated our headquarters to southborough, ma. They are serious about scientific integrity and have a dynamic company culture, including a focus on work-life balance. Value proposition for you: * flexible work schedule. * proven potential for professional growth. * a community of brilliant minds at your disposal. * the stability of working for a robust, financially sound cro that is growing at a sustainable pace. * exposure to more than 20 therapeutic areas, including cutting edge therapies such as immuno-oncology, biosimilars, gene therapy, and new molecular entities. As the vice president, biometrics you will… * be a critical part of the global core leadership team by being responsible for the guidance and strategic direction of the global biostatistic and data management teams. * advance the overall success and future growth of our client by having executive contact with current clients, providing key client oversight and strategic project contribution, and contributing to new business development. * develop and implement department strategies to increase productivity and quality, while decreasing cycle times and costs. Oversee the data management and statistical aspects of client projects and project teams. * participate in presentations of capabilities and research proposals to prospective clients. Represent data management and biostatistics in marketing efforts by developing project bid proposals, participating at bid defense meetings, or performing client presentations. * provide oversight of the hiring and management of personnel. Ensure that adequate training occurs and that performance evaluations are completed. * and much more! education: degree in statistics, biostatistics, math, or a related field. Phd or master’s degree preferred. Experience: * at least 15 years of relevant work experience and at least 5 years of supervisory experience. * experience in a leadership position within biostatistics or data management for a cro. * have previously contributed to the overall strategic direction of a company or business unit. * thorough knowledge of ich gcp guidelines and other applicable regulatory rules and guidelines and of medical terminology, clinical trials, and clinical research. * working knowledge of the relationship and regulatory obligation of the cro industry with pharmaceutical/biotech companies.

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    Guillermo |Software Developer

    Let me know if you need an expert in Scientific Computing and Scientific *****times we...

    59 Minutes Later
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    Serge |President

    I am the former Manager, *****tegy at Bio-Rad *****, where I was responsible for t...

    1 Hour Later
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    Jean |President-Consultant

    Hello, I have been involved as manager of clinical *****gement and biometrics for 25 years, mai...

    22.4 Hours Later
+27 Other Responses
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Contract Research Organization Market

We are an established, us-based firm researching the cro (contract research organization) market, specifically providers focused on data management and biostatistical services. We are interested in speaking with business development professionals from the cro industry as well as c-level executives from the biopharmaceutical industry. Note: we seeking professionals from boutique to mid-size organizations (e.G. Generic pharmaceuticals, boutique cros and biopharmaceutical companies with less than $100m in revenue) rather than those with "big pharma" or top-tier cro experience. Please include your relevant experience in this space, and where you fit within the above specifications.

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    Spencer |General Manager

    Looks like a good fit with our skills and experience. Need more details: Length of interviews. N...

    35 Minutes Later
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    David M. |Director

    Bio-Medical Consultants & ***** a small contract research ***** have been in busi...

    1.8 Hours Later
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    Vadim |Senior Director, Clincal Research

    As a Program Director I am in charge of identifying clinical research program needs, suitable vendor...

    2.2 Hours Later
+33 Other Responses
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Pharma Research Interviewees

We are seeking highest specialized experts with experience in the life sciences industry - must meet below specifications location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston. Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research. Testing availability: late june - early july study 1: qualitative study - focus group interviews with 3 groups (6-8 respondents per group) **respondent profile**: group 1: 6-8 pharmaceutical executives from top 20 biotech companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/clinical research organizations (cros). Group 2: 6-8 pharmaceutical executives from top 10 clinical research organizations (cros) companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations. Group 3: 6-8 pharmaceutical executives from small / mid-sized pharmaceutical companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations. **expert must have** a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others): a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management. E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc. F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.

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    Jukka |President, Director

    My experience covers all areas over 30 years. Have a look at my profile. I have recently consulted o...

    27 Minutes Later
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    Scott |Sr. Technical Services Project Engineer

    I am involved in most of the areas you need help with. I oversee all of our 3rd parties. Let me kno...

    45 Minutes Later
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    Kuldeepak |Director

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

    53 Minutes Later
+15 Other Responses
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Cro Outsourcing In Clinical Trial

We are a market research company looking for the following information pertaining to cros on behalf of our client: unique cro outsourcing trends in the clinical trial (cro) industry where cros have been innovative in how they offer services to pharmaceutical companies; real life examples between cros and pharmaceutical companies preferred or approved supplier for major pharmaceutical companies how other pharmaceutical companies validate cro rates without going out to bid? Supplier analysis and market analysis

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    Vijay |Clinical Project Manager

    Hi I have more than 10 years of experience working with pharmaceutical/biotech and medical device ...

    4.5 Hours Later
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    Antonio |Director Laboratory Medical Microbiology

    My experience is limited to Swiss companies CROs....

    5.7 Hours Later
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    Jukka |President, Director

    Hello - I have more than 30 years of experience working with CRO and been on the CRO side as well. M...

    5.7 Hours Later
+24 Other Responses
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Contract Research Organizations

We would like to speak with an expert who can help us in gathering the information on cros direct cost data for specific cro services. We would like to cover cost per site and cost per patient estimates based on the following parameters: geographical focus: north america and western eu services required: • site feasibility • site identification • site qualification • site initiation • essential document collection • site management • site monitoring • project management

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    Joan |Principal and Founder

    Hello, I believe I am qualified to assist you with your inquiry. I have worked 10+years in the CRO ...

    6.7 Hours Later
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    A D |Clinical Research & Medical Affairs Prof

    I am giving below the contact of an expert in this realm: Dr Arun Bhatt Email: *****....

    6.7 Hours Later
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    Shyam |CFO Advisor

    Hi Rithika Just made a CRO selection for Axiomed (at KICVentures). I can assist with this Shyam...

    7.1 Hours Later
+15 Other Responses
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Contract Research Org (cro) Price Benchmarking

We are a global market research firm, currently looking for experts who can assist us in price benchmarking of various types of tests conducted by cros (contract research organizations) the types of tests in which we are interested are given below: clinical routine labs (e.G., chemistries, lipids, hormone levels, viral serologies/pcr, vitamins, heavy metals) genomics whole-genome sequencing genomics rna sequencing genomics metagenomics genomics methylation assays immunology cytof immunology flow cytometry immunology tcr/bcr sequencing proteomics targeted affinity-based proteomics proteomics untargeted mass spectrometry proteomics targeted (mrm) mass spectrometry metabolomics untargeted mass spectrometry metabolomics targeted (mrm) mass spectrometry we are looking for an expert to discuss the points mentioned above. Ideal candidates should have deep knowledge of prices offered by different cros kindly drop in a note with your cv/relevant experience in the pharmaceutical industry, if you are interested to proceed. Best regards, thomas

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    Terry |President

    I am the former Global Director of Biomarker R&D and Scientific Affairs for Quest Diagnostics, one o...

    2.4 Hours Later
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    Eugene |Scientific Director

    Dear Thomas, hello. I'm Director of CRO. We can help you....

    2.5 Hours Later
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    Katerina |Scientific Team Leader, Account Manager

    I can provide you with some pricing points for pre-clinical CRO, based on my experience as Business ...

    2.5 Hours Later
+40 Other Responses
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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.

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    Shridhar |Honorary Adjunct Faculty

    I have significant experience in early clinical development and could provide insights on Indian and...

    2 Hours Later
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    B |

    I am a Clinical Pharmacologist and Entrepreneur with over 15 years of experience in drug & biotech d...

    2.3 Hours Later
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    Nikolina |Regulatory Affairs Manager

    Please note my inerest for Your project. Nikolina Angelova...

    2.5 Hours Later
+23 Other Responses
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