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

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Recent Health Informatics Inquiries

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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 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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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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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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Radiology And Cardiology Informatics

Cardiology informatics companies

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    Dr. Sheila |CEO and Founder, Partner & Shareholder

    I am a practicing cardiologist that has a consulting firm. Please see the ***** website a...

    4.1 Hours Later
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    Gregg |CTO

    Can you provide a little more context?...

    6.2 Hours Later
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    Eric |President

    RadictGb2K, My background includes *****ees in Radiologic Technology, and Information ...

    7.4 Hours Later
+4 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 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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Blinded Clinical Trials

I am looking for an expert who can guide me about the un-blinded monitoring process in blinded clinical trials and help me understand how pharma companies approach un-blinded monitoring. Do they source from a single supplier/multiple suppliers or do they appoint an in-house un-blinded monitor. Please get in touch asap. This is a little urgent. Thanks!

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    Xavier |CEO

    I have a long experience of blinded clinical trial, even when blinding is challenging or even impos...

    10 Minutes Later
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    Vijay |Clinical Project Manager

    Hi there, I have experience in managing clinical trial project in different settings, industry & ac...

    2 Hours Later
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    Susanne |Independent Consultant, Director, Vice P

    Hi for your background ***** get up to speed, look into FDA's web site drugs side and check...

    4.7 Hours Later
+11 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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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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Software Engineering

Software engineer with extensive experience reviewing and drafting us patent applications related to radiology health informatics and in health information interoperability. We need an engineer to review existing patent portfololio and assist in drafting the technologic descriptions of spinoff patent applications.

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    Ilya |Patent Attorney

    I am a *****rney registered to practice before the U.S. ***** Trademark Office. I also wo...

    8 Minutes Later
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    Jeff |Head of Installable Apps

    I'm a good software engineer and have an excellent background in *****. I do not have the Radiolo...

    11.2 Hours Later
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    David |Executive Consultant, CSA, CEO

    Have over 8 years in ***** background as a legal expert (and specifically challenges to same)....

    11.7 Hours Later
+12 Other Responses
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Late Phase Clinical Trials

Clinical trials - late phase studies cost benchmarking hello, we are looking for experts in the late phase (phase 4, post marketing) area of clinical trials. We wish to perform cost benchmarking and kpi benchmarking for different aspects of phase 4 studies. We also want to understand the sourcing practices for different scenarios e.G. (tactical vs. Strategic; local vs. Global etc.)the details are mentioned below. Deliverables: • per submission cost benchmarking for cta submissions • per dossier cost benchmarking for dossier publishing • per patient cost benchmarking for interventional trials • per patient cost benchmarking for nis trials • key service level kpis and performance benchmarks • sourcing practices for different scenarios (e.G. (tactical vs. Strategic; local vs. Global etc.)) therapeutic areas: (oncology, respiratory, neuroscience, infectious) geographies: india, china, uk, brazil regards, vimal

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    Stefano |Board Member

    I can support you on almost all items of your list except for the geography. I would propose to work...

    2.8 Hours Later
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    Barbara |CEO, Senior Consultant

    Hello, I have experience in all of the required fields and will be able to suppor your projects. B...

    14.6 Hours Later
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    Yevgen |Scientific Director

    Hello. I'm Director of CRO. Can do this job by e-mail...

    2.8 Days Later
+11 Other Responses
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