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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 Medical Trials Inquiries

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Clinical Evaluation

I'm looking for assistance in writing/creating a clinical evaluation for a class i medical device.

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    Susanne |Independent Consultant, Director, Vice P

    I have written many of them for my clients for the CE Mark ***** to renew their certificati...

    4 Minutes Later
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    Trina |Medical Writer

    Hello: I have extensive experience writing Class I and Class II Clinical *****rts. I hav...

    15 Minutes Later
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    Neil |Senior Medical Outcomes Liaison

    Our firm has years of experience *****e documents. ...

    1.7 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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    Saurabh |Founding Advisory Doctor

    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...

    56 Minutes Later
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    Swamy |Medical Writer

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

    56 Minutes 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...

    57 Minutes Later
+21 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...

    1.8 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...

    13.6 Hours Later
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    Yevgen |Scientific Director

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

    2.7 Days Later
+11 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, ...

    44 Minutes Later
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    David |CEO/Medical Director

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

    55 Minutes 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...

    1 Hour Later
+54 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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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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Clinical Trials Project Management

I'm looking for an experienced project manager to assist with a phase i/ii clinical trial in the sf bay area. Must be willing to perform detailed project management tasks while being able to assist with strategic planning as well.

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    Dean |Advisor - Board of Directors

    I am a member of a Project Management group that will be able to support your clinical trials, regar...

    8 Minutes Later
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    Patrick |Consutant Physician

    I am interested to get involved....

    18 Minutes Later
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    Yair |Owner and CEO

    Dear CEO My name is Yair Alegranti and I have an extensive clinical trials experience both pharma...

    24 Minutes Later
+33 Other Responses
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Early-stage Oncology Clinical Trials

Consultant type: oncology clinical trial managers, organizers, site coordinators, trial investigators/consultants; oncology clinical trial regulatory personnel; clinical project manager/consultant at cros and pharmaceuticals priority regions of interest: united states, europe, india few companies involved in this space: cros conducting early-stage oncology clinical trials (e.G., lambda therapeutic research, labcorp, ppd, iqvia, syneos) few clients involved in this space: small-to-mid-sized pharmaceutical companies in oncology field (e.G. Novartis, amgen, astrazeneca, bms, biocon, incyte) the some of the key aspects that we are looking to understand from the experts are (global and india): o market size and segmentation (value and volume) of oncology clinical trials: • historic & future growth rate • market trends/drivers & challenges • impact of covid-19 on the market demand o regulatory overview of the indian clinical trial market: • regulatory submission and approval process • necessary sops– protocols & guidelines: prerequisites to conduct a clinical trial in india for indian and foreign molecules and medical devices • mapping of application and approval process: clinical trial commission, trialist and registrant application, necessary documentation required, phase i / ii data review, feedback and institutional ethical committee approval o assessment of market structure and identification of key cros • evaluating the market structure for the early- stage oncology trials by the cros and sponsors • identification of key cros that conduct the early- stage oncology ct globally and in india • competitive assessment of key cros (lambda research / labcorp / ppd, etc) • business overview and offerings of the key cros in this space • information on technologies used for patient recruitment, risk based monitoring, patient monitoring, etc. • proficiencies in biostatistics and statistical programming, clinical data management • business model and strategic outlook within the oncology space • type of customers and services provided o customer assessment • identification and segmentation of the key customers (mid – small pharma clients) • evaluating current and future customer requirement and challenges faced by them

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    Athanasios |Planning Officer at Department of Pharma

    I am an expert on oncology clinical trials...

    61.2 Days Later
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    Reinhold |Senior Director, Head of Genomic Biomark

    9 years experience in clinical trial (oncology) management ...

    61.2 Days Later
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    Lokesh |Program Director

    I work in clinical oncology space and will be happy to help you. I have 10 years experience in manag...

    61.2 Days Later
+32 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...

    17.7 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...

    20.9 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 ...

    20.9 Hours Later
+17 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 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...

    1.1 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...

    1.2 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) ...

    1.5 Hours Later
+16 Other Responses
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