Source Cro 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 a Demo

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 Cro Inquiries

Area Icon

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

  1. Profile Picture

    Hong |Executive director

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

    52 Minutes Later
  2. Profile Picture

    Laura |Experienced Clinical Research Consultant

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

    53 Minutes Later
  3. Profile Picture

    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
Area Icon

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

  1. Profile Picture

    Vijay |Clinical Project Management Consultant

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

    13 Minutes Later
  2. Profile Picture

    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
  3. Profile Picture

    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
Area Icon

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.

  1. Profile Picture

    Jukka |President, Director

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

    29 Minutes Later
  2. Profile Picture

    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
  3. Profile Picture

    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
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

    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

    1. Profile Picture

      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
    2. Profile Picture

      Rishit |Executive

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

      16.8 Days Later
    3. Profile Picture

      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
    Area Icon

    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.

    1. Profile Picture

      Guillermo |Software Developer

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

      59 Minutes Later
    2. Profile Picture

      Serge |President

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

      1 Hour Later
    3. Profile Picture

      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
    Area Icon

    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

    1. Profile Picture

      Terry |President

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

      2.4 Hours Later
    2. Profile Picture

      Eugene |Scientific Director

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

      2.5 Hours Later
    3. Profile Picture

      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
    +39 Other Responses
    Area Icon

    Clinical And Regulatory Medical Writing

    This is a full-time employment opportunity onsite in southborough, ma. **as a manager, clinical and regulatory medical writing you will: - implement project-specific strategies and assist with the development and implementation of department strategies to increase productivity and quality. - assist with the oversight of medical writing personnel. This includes hiring personnel, managing personnel matters, conducting performance evaluations, and training medical writing staff regarding applicable regulatory guidelines and medical writing practices. - assist with resource allocation and the development of business proposals related to the medical writing functions. - be responsible for the smooth functioning of all medical writing projects for clients and project teams through management of internal staff and the medical writing process. - serve as the lead medical writer on projects when appropriate. As the lead medical writer, you will draft and finalize documents necessary for all phases of clinical drug and device development, work with project managers to develop timelines and resource plans for the production of clinical documents, review statistical analysis plans and crfs, and perform peer and qc review of clinical study reports and clinical sections of regulatory submissions written by other medical writers. - and more! **required education and experience**: - bachelor’s degree or advanced degree, with some applied training relevant to the clinical trials or health research environment. - at least 5 years of medical writing experience in a cro, pharmaceutical, or biotechnology setting. Management experience preferred. - 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. - familiarity with moderately complex statistical methods that apply to phase i-iv clinical trials. **about our client** 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. They are serious about scientific integrity and has 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. Note: please attach your latest cv along with your response on zintro.

    1. Profile Picture

      Ivan |Zintro Expert

      November 9, 2015 Dear Sir / Madam I am very interested in the position of Manager, Clinical and Re...

      6.1 Days Later
    2. Profile Picture

      Gayatri |Zintro Expert

      I am interested...

      14.6 Days Later
    3. Profile Picture

      New |

      Dear Hiring Manager, I am submitting my resume for ***** the position of clinical and ...

      21 Days Later
    +18 Other Responses
    Area Icon

    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

    1. Profile Picture

      Vijay |Clinical Project Management Consultant

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

      4.5 Hours Later
    2. Profile Picture

      Antonio |Director Laboratory Medical Microbiology

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

      5.7 Hours Later
    3. Profile Picture

      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
    Area Icon

    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

    1. Profile Picture

      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
    2. Profile Picture

      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
    3. Profile Picture

      Shyam |VP of Finance

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

      7.1 Hours Later
    +15 Other Responses
    Area Icon

    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.

    1. Profile Picture

      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
    2. Profile Picture

      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
    3. Profile Picture

      Kuldeepak |Director

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

      53 Minutes Later
    +15 Other Responses
    Area Icon

    Therapeutics Clinical Operations

    Director, clinical operations. This is a full time employment opportunity in california,usa. Provide key clinical support for the operation and execution of clinical trials for clinical programs. Ensure compliance and completion of the following clinical drug development activities: -requires minimal supervision to manage various activities associated with multiple clinical studies -working knowledge of fda regulations and ich guidelines to ensure compliance with both during clinical trial conduct -has had experience as clinical operations lead on significant phase i or phase ii programs -participates in evaluation and selection of cro’s, contractors and other outside vendors, and the development of budgets. Manages cros and vendors, as appropriate -manages efforts in study start-up, including study feasibility, site selection, preparation and follow-up of site regulatory packages in partnership with the director of oncology clinical development -independently designs or assists in the development of study related documents including but not limited to: case report forms, case report form completion guidelines, study manuals and project tools, monitoring plans, tracking tools, informed consent forms, and study reports -may prepare study-specific training materials or slides for investigator meetings -contributes as part of the clinical protocol development team requirements: -ba/bs in science-related field with 10 + years’ experience in clinical operations /trial management or a combination of relevant related work experience -demonstrated thorough understanding of fda regulations and gcp and proven success record in managing trials

    1. Profile Picture

      Matthew |Division Medical Officer

      Very interested, qualified, and experienced. Resume available....

      42 Minutes Later
    2. Profile Picture

      Terry |President

      I am interested in this position. I previously held the position of Director of Biomarker R&D and S...

      1 Hour Later
    3. Profile Picture

      Bonnie |Medical doctor self employed Infectious

      Very experienced MD with many years in research and clinical practice . Looking forward to communi...

      3.8 Hours Later
    +19 Other Responses
    See More Inquiries

    Top Cro Experts

    See More Experts
    Share
    LinkedInTwitterFacebookGoogle+