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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.
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Recent Clinical Trials Inquiries

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Clinical Trial Investigation

I'm looking to talk to clinical trial principal investigators, medical researchers who have run or are running clinical trials, about their experiences.

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    Christopher |Zintro Expert

    I have extensive experience with clinical trial design and execution as well as is endpoint design, ...

    1.7 Hours Later
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    David |CEO/Medical Director

    I have 10 years of principal *****rience and would be happy to assist. ...

    1.9 Hours Later
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    Humberto |VP Clinical Research / Pharmacovigilance

    I have over 25 yers of experience in practically every phase of clinical research, although mostly l...

    2.1 Hours Later
+54 Other Responses
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Standard Operating Procedures For Clinical Trials

• aim is to create an sop for clinical trial diversity - human trials; procedures to follow, develop a program which becomes standard for future trials and diversity elements are incorporated in each trial • potentially rates for this kind of consulting work

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    Steven |Principal

    My previous role was as a clinical research director in a region of the country where we needed to f...

    1.9 Hours Later
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    Swamy |Medical Writer

    Define the scope, elements to cover and page length. ...

    1.9 Hours Later
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    Tasha |Project Director

    I have a lot of recent experience in the last 18 months promoting trial diversity by selecting and s...

    2 Hours Later
+21 Other Responses
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Oncology Clinical Trial

We would like to understand the % difference of per patient cost for oncology clinical trial and a rollover oncology trials.

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    Veeramani |Marketing Head

    I can help you...

    18.7 Hours Later
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    Andrea |Clinical Research Consultant

    Having set up many oncology clinical trials I can give feedback from a UK perspective...

    21.9 Hours Later
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    Athanasios |Planning Officer at Department of Pharma

    I am an expert in oncology with a scientific background in clinical trials. My master degree at the ...

    21.9 Hours Later
+17 Other Responses
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Clinical Trial Compliance

Looking for consultants on areas like clinical trial compliance with 20+ years experience. To know more feel free to contact me.

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    Adam |VP Clinical Operations and Strategy

    I have 21 years of experience in this area. Let me know what I can help you with. Regards, Adam Rusk...

    2.1 Hours Later
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    Bonnie |Medical doctor self employed Infectious

    I have over 35 years Clinicsl trial experience as infectious diseases MD Thank you very much Bonn...

    2.2 Hours Later
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    Jorge |Clinical Research Expert

    To tell the truth, I have 16 years of experience. Please see my CV at LinkedIn (Jorge Timoteo) ...

    2.5 Hours Later
+16 Other Responses
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Clinical Trials Ai Platform

We are looking for experts who can provide their insights and feedback to a startup seeking equity investment. Startup description: design & conduct better clinical trials. Making clinical trials seamless by bringing together the best and most important functionality of study design & protocol optimization, trial administration, data collection & task management all in one intelligent system. Experts that have interest, knowledge or background in: industry: healthcare, clinical trials, pharmaceutical, life sciences, health and wellness technology: healthcare it, deep learning, ai, end-to-end platforms who we are: we are an online investment platform working to provide a fair and transparent process for startup evaluations and that selects the companies that will outperform other startups in the next three to ten years. Who you are: you do not need to be an experienced angel investor to be a valuable member of the evaluation team. We seek a diverse group with expertise that may cover the market, business model, technology and customers of the startup company. However, if you are an accredited investor, you have the option (but not an obligation) to invest as little as $1000 fee- and carry-free in the startup company if the resulting evaluation leads to an investment. What you will do: as a participating evaluation team member, you will answer a set of questions and rate the comments and feedback of other evaluators. (this is an all volunteer community of industry experts and investors that evaluate startups, requiring about 2 hours total of your time over about 2 weeks.) what’s in it for you: - an inside look at cutting-edge technology or go-to-market approaches - introductions to company management, upon request - collaboration with like-minded experts who are on your evaluation team - contributing to creating a fairer, more-informative process for startups seeking investment

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    Steven |Principal

    I have experience in the healthcare and clinical research fields and would like to take part in this...

    2.3 Hours Later
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    Vijay |Clinical Project Manager

    Hi I have more than 14 years of experience in clinical trial ***** have helped designing i...

    2.4 Hours Later
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    Gabe |Clinical Trial Consultant

    I have extensive experience, and happy to help....

    2.5 Hours Later
+29 Other Responses
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Clinical Trial Outsourcing

Would like to understand the clinical trial activity list phase wise and activities that could be worked in advance by the sponsors to speed up the trials, while outsourcing to cro's ?

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    Andrew |Clinical Research Manager

    Interested. I'm familiar with all aspects of clinical trials outsourcing....

    10.9 Hours Later
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    Debashis |Oncology-Clin Sciences & Ops -Director

    Yes. For last 20 yrs, I have been doing it. Plz ask them to call me to schedule an appointment ...

    10.9 Hours Later
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    Iyore |Global Trial Manager

    Interested I have worked on all aspects of clinical trials outsourcing in all phases of clinical tri...

    11 Hours Later
+19 Other Responses
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Clinical Trial Operations

Our client would like to speak with industry experts who have experience in managing clinical trial operations including decentralized clinical trials. They are looking to identify opportunity areas for connected injectors, especially in decentralized clinical trials (phase ii and phase iii). Target geo: north america and europe if open to participating, kindly answer the below questions. In your role, are you involved in managing decentralized (virtual/hybrid) clinical trial operations? Do you have experience in managing clinical trials for sub-cutaneous injectable drugs? On a scale of 1-10, please share your level of knowledge about syringe/auto-injector / pen injector / patch injector use in clinical trials on a scale of 1-10, how involved are you in the implementation of digital solutions such as connected devices, wearables in clinical trials? Are you involved in the clinical trial operation of any of the following list of therapy areas ( oncology, diabetes, auto-immune, central nervous system, respiratory,) please note: our client is only interested in your personal point of view and is not seeking confidential information.

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    Laura |Sr. Clinical Trial Manager

    In your role, are you involved in managing decentralized (Virtual/Hybrid) clinical trial *****?...

    3.3 Hours Later
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    Betro |Hospitalist / Informatician / Steering C

    Not my area of expertise ...

    4.6 Hours Later
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    Dr Chalres |Founder and Principal Advisor

    I have 12 years experience in global clinical trial ***** can speak to this. In your rol...

    7.5 Hours Later
+11 Other Responses
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Pricing Models For Phase Iii Clinical Trials

We are conducting a study on the various pricing models prevailing in the industry for phase iii clinical trials and also how is the milestone pricing model being adopted and received currently. Would be glad to understand on the various milestones/ goals that are setup for the periodic payments in the milestone model and also what are the various payment/ pricing models prevalent in the industry?

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    Andrea |Clinical Research Consultant

    happy to feedback. Extensive experience of Uk pricing for several different PHIII trials...

    2.5 Hours Later
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    Athanasios |Planning Officer at Department of Pharma

    I am open to work on this project. I have vast experience in the Pricing and reimbursement of innova...

    2.6 Hours Later
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    Mathini |Principal Consultant

    Hi there, I have over 10 years of procurement and supply chain consulting experience, and work with ...

    2.8 Hours Later
+8 Other Responses
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Clinical Trial

This is a full-time employment opportunity for a clinical trial manager (ctm) in the san francisco area. -responsible for coordinating and monitoring the day-to-day logistics of our clinical trials. Functions: -manage clinical trial operations including vendor performance, internal/external metrics, and communication of project status within the project team -manage and track completion of study start-up, conduct, and closeout activities to industry and corporate standards -ensure the progress and completion of projects according to timelines -prepare and present project specific updates -lead or assist in the writing of clinical documents such as protocols, study reports, study manuals, and annual reports -monitor safety surveillance and reporting activities -oversee data management processes including collection and cleaning of clinical database, reconciliation of clinical and safety databases, and data interpretation and evaluation -coordinate dsmb/safety reviews inline with charter and overall study parameters -assist in the construction of clinical development processes including development and writing of sops, creation and organization of study trial master files, and clarification of organization and workflow structures -plan, generate, and track study timelines and trial budgets -site management activities including: review monitoring reports, interact with study monitors, track site errors or other indicators of site difficulties, identification of potential problem sites and development of corrective action plans as required, acting as our contact, as needed, for clinical sites experience: -ba/bs degree in biological science or nursing required (equivalent experience may be accepted) -5+ years of clinical research in the biotechnology/pharmaceutical industry -3+ years of multi-center clinical trial management experience, specifically experience in phase 2, phase 3 us & international clinical trials -experience managing cros, central laboratories, and other clinical study vendors -experience preparing clinical trial budgets and contracts -knowledge of ich-gcps and 21 cfr is required -experience in metabolic/hepatic drug development is desirable -experience with ivrs and/or edc is desirable

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    Arthur |Director

    To whom it may concern, I am currently Director of drug development at a small biotech firm, Bellus...

    1 Day Later
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    Dr Saurabh |Head of Hospital Operations

    I have been involved with *****ures including research on ***** a drug. Please c...

    1.5 Days Later
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    Mike |Clinical Research Coordinator

    Dear Sirs: I feel that I would be an outstanding ***** this position based on my work histor...

    2.1 Days Later
+24 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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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

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    Matthew |Division Medical Officer

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

    1.7 Hours Later
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    Terry |President

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

    2.1 Hours Later
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    Bonnie |Medical doctor self employed Infectious

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

    4.8 Hours Later
+19 Other Responses
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Board Medical Chair

This is an opportunity for a dedicated medical professional to join our mission of protecting human research subjects as a board chair in our puyallup, washington location. Please note: we are seeking to hire a full-time employee and are not interested in responses from those only interested in consulting. Must be authorized to work in usa without visa sponsorship **position summary**:  - provide the highest possible support to our ethical review and research safety programs in areas and issues requiring medical training and judgment. This most commonly involves the institutional review board, and may also include providing medical advice to biosafety committees. **essential duties & responsibilities**: - chair board meetings to ensure compliance with federal and state laws as well as our policies and procedures, and facilitate discussion from board members. Provide scientific, ethical and regulatory support and advice to board members - analyze and present protocols and other agenda items at board meetings to facilitate informed decision making. Set standards and role model effective presentation and discussion for all board members. - analyze research submissions, identify problems and issues, collect additional information or request corrections, and draft memoranda. - research, draft, and present reports to the board on a wide range of topics, including but not limited to, investigator misconduct, site visits, fda and sponsor audits of investigators and others, issues involving human subjects, sponsors, and institutions. - advise clients of applicable scientific information and regulations pertaining to human subject research, both orally and in writing. - analyze requests for exemption determinations and provide formal written opinions that proposed projects are exempt from the requirements for irb review or do not require irb review. - provide guidance to clients to help resolve scientific, ethical and regulatory issues and difficulties. - review literature and other materials to keep abreast of developments in the regulatory, legal, and ethical arenas. **educational qualifications**:  - md or do - list the medical licenses you currently hold or have held in the u.S **qualifications/experience requirements**: - experience in submitting and/or reviewing clinical trial protocols is strongly preferred. This experience is normally gained while working in the clinical trial industry or as an irb board member. - experience as a member of an medical ethics review board would be relevant. - able to chair board meeting and effectively present information to a diverse group of professionals - six or more years of related clinical experience and/or training, preferred - ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. - knowledge of ms word, ms excel, ms outlook and ms windows. Please note: we are seeking to hire a full-time employee and are not interested in responses from those only interested in consulting. Must be authorized to work in usa. Kindly respond providing a brief summary of your relevant experience and attach your latest resume on zintro.

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    Hong |Expert Physician

    Hi I am interested in this position, I have over 20 years experience in clinical, medical, et al. I...

    27 Minutes Later
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    Lola |Vice Presidentt and Strategic Developmen

    Dear Sir/Madam, I'd like to be considered for this position. Solid academic background (MD/PhD in Cl...

    1.3 Days Later
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    Joseph |Pharmaceutical Consultant

    I am a cardiologist with extensive clinical trial experience in both academia and the pharmaceutical...

    1.6 Days Later
+45 Other Responses
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