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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 Clinical Inquiries

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Clinical Data Science Market

Hi, i am a research analyst working with a global market research and consulting firm based in the u.S. And our asian intelligence center is situated in india. We publish strategically analyzed market research reports and serve as a business intelligence partner to fortune 500 companies across the world. Right now i am studying the “life science & clinical data sciences market - product and vendor landscape analysis”. The following software solutions have been covered in the scope of this research study: “clinical data repository/ warehouse, metadata repository, clinical analytics & reporting platform, clinical decision support portals/analytics dashboards, integrated data sciences platform, and clinical data integration platform” i would like to have a short discussion to understand the dynamics and future prospects of this market. I have already done some research in this market and would be sharing my research findings as well. As a token of appreciation, we would be sharing a copy of executive summary (containing key analysis results) of this research study once the project is done. I would appreciate if anybody can help me with this research study. As we have a stipulated time factor for this project, we look forward for the interview at the earliest possible. Thanks & regards, riya

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    Kuldeepak |Director

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

    1.9 Hours Later
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    Ranjit |Sr Marketing Manager Exports

    Yes I can help you. Presently I am helping few companies from USA and ***** do their Clinical da...

    3.4 Hours Later
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    Barry |Professor

    I was CSO IBM Global Healthcare, Pharmaceutical and Life Sciences, including market analysis and fut...

    3.9 Hours Later
+8 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 Decision Support (cds) Systems

Looking for experts knowledgeable about the clinical decision support systems market in the us. Key topics of discussion are - • overall market ecosystem for cds systems • market size and growth • criteria for selection of cds systems/tools • market trends and regulations • integration with other systems such as electronic health record systems • impact of cds on radiology benefits management systems • leading players who are offering cds systems

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    Joseph |President & CEO

    I do not have strong knowledge of specific vendors but can speak to the topic from a market perspect...

    3.9 Hours Later
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    John |Director of Revenue Cycle Products, Sale

    I work at Epic, the largest EMR and CDS vendor in the US. My role consists of three job functions t...

    4.4 Hours Later
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    Japa |Vice President of Operations

    I have worked to develop CDS systems for our physician speciality group (200 providers). Integrated ...

    4.9 Hours Later
+22 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 Attrition And Turnover Rates

Hello, i would like to understand benchmarking turnover / attrition rates at companies functioning out of service centers in india (specifically mumbai) for the staff profile below: md degree with 2 years of clinical experience; or phd, pharmd, dpm, or dvm degree with 3 or more years in clinical settings, or ms, bs rph, rn hcp or life science degree plus 3 or more years of pharmacovigilance experience and 2 years of clinical experience. • detailed knowledge of drug safety processes • basic knowledge of ich principles of sae/ae reporting along with basic understanding of local and global regulatory roles and regulations. • basic knowledge of safety policies and procedures in the major countries • high sense of responsibility and accountability and special sense for diligence even for routine processes • proactive behavior and being able to keep timelines • good knowledge of ae and drug coding conventions (meddra, who-dd). • interpersonal skills. • good oral and written communication skills are essential, including fluency in english. . • ability to identify problems in case evaluation and to assist in the design workable solutions • basic knowledge of standard office software packages (word, excel).

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    Polina |Oversight & Monitoring Lead, Health Care

    I am highly involved in India's drug safety and product complaints processing. I am knowledgeable in...

    1.9 Hours Later
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    Ranjit |Sr Marketing Manager Exports

    I have good knowledge of Indian Pharma Industry and Pharmacovigilance. But I am not clear about, wh...

    14.3 Hours Later
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    Elizabeth |Zintro Expert

    I have been working with clinical *****ice providers since 2007. I have experience in team...

    3 Days Later
+4 Other Responses
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Clinical Research

Looking for subject matter experts / consultants in clinical research, clinical trial, risk management, audit and inspection, gcp, clinical outsourcing, trial design and management,ethics fraud and misconduct, patient recruitment , documentation and management, clinical laboratories, facility/hospital , hospital clinical compliance, billing and coding for clinical services , patient/third-party coding and billing, sponsors, cros, clinical quality control/cqc for speaking engagements with over 25+ years of experience. Feel free to reach out to me.

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    Gabe |Clinical Trial Consultant

    I have experience in many of these areas www.g2crc.com...

    9 Minutes Later
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    Jeffrey |President and Managing Director

    I am an MD (certified in internal medicine)/PhD (basic pharmacology) with 30 years of pharmaceutical...

    10 Minutes Later
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    Victor |Director

    I have >20 yrs experience. Victorchen22 at *****...

    14 Minutes Later
+20 Other Responses
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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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Clinical Quality Assurance

We're looking for a clinical quality assurance auditor: must have: 1. Gcp or gxp auditing experience in a cro, pharma, or biotech setting. 2. The ability to travel 3. General knowledge of regulations: 21 crf part 11, gcp guidelines & standards. -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 a clinical quality assurance auditor you will: -assure that processes, quality systems, and inter-location synchronization within are aligned to promote an efficient working environment that follows compliance to regulations, standards, and good gcp guidance and provides clear pathways for inquiry, reporting, and resolution through audit, the capa process, and quality metrics. -serve as liaison for quality compliance to all locations providing oversight from a corporate level. -write and issue audit reports and communicate audit findings to relevant project team members and/or functional area management. Administrate the controlled documentation program by reviewing, revising, and writing sops. -identify inefficient or outdated working procedures, develop revision plans, and conduct future review to determine the success of the procedure modifications. -travel to multiple locations to conduct internal audits. Travel to suppliers to conduct vendor qualification and assessment audits. And more! education -bachelors degree in a science or related field. Experience -at least 3 years of cro or pharma related experience. -at least 2 years of relevant gcp auditing experience in a pharma, medical device, cro, or similar environment. -general knowledge of relevant regulations including 21 crf part 11 and gcp guidelines and standards. -asq-cqa or similar certification desired.

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    Vanessa |QA/RA Professional

    Good morning, I believe that I can fit the profile you are looking for. ...

    54 Minutes Later
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    Ravi |Director / Manager , Solution Architect,

    Hello, This requirement is right in my ally of expertise, having assisted Dow30 Pharma/Biotech/Med ...

    1.2 Hours Later
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    Victor |Zintro Expert

    Afraid I can not help here. V...

    1.3 Hours Later
+33 Other Responses
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Sas Programmer Life Sciences

Full time individual minimum 5 years sas programming experience in pharmaceutical industry/cro in the us or eu. • 7 years experience strongly preferred. • strong knowledge and solid understanding of clinical trials. • able to critically review protocol, statistical analysis plan for statistical/programming needs. Experience in programming of statistical outputs a must. • experience with regulatory submissions and integrated summaries. Extensive experience with validating outputs of others. • proficient in sas macro, cdisc, sdtm, and adam. • strong programming, analytical, project management, verbal, written communication skills. • track record of successful management of technical projects like e.G . Leading programming for assigned clinical studies. • able to work with minimal supervision. • effective under pressure: can meet timelines and provide high quality deliverables.

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    Elizabeth |Research Scientist

    I am a SAS programmer. I have used SAS in my research work for many years. I have taken courses in c...

    41 Minutes Later
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    Eunpa |Statistical and Research consultant

    I have five years of experience in programming with SAS in *****arch work and return-o...

    53 Minutes Later
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    Pushap |CEO, MD

    I can work on this project as i have all the variables required by you. • 6 years experience. • St...

    4.1 Hours Later
+13 Other Responses
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Clinical Laundry Service In Uk

I looking for information pertaining to clinical laundry service cost across uk specific to norfolk and norwich area.

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    Antonio |Director Laboratory Medical Microbiology

    Sorry, I am not an expert in clinical laundry....

    5.9 Hours Later
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    Michael |CMSO , Chief Medical Strategies Officer

    We currently produce clinical garb that would be laundered differently and is anti microbial. Maybe ...

    6 Hours Later
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    Patrick |Executive Director, Heart and Vascular S

    Not a candidate...

    15 Hours Later
+6 Other Responses
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Clinical Nurse Leaders

Looking for clinical nurse leaders (cnl) or nurse hiring managers who can speak to the cnl position. I'm looking for a phone consultation to better understand who is hiring cnls, perceptions of the position, and expectations for job demand in the future.

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    Cindy |Director of Risk Management and Corporat

    I have been a Registered Nurse for over 30 years. I have ***** Director of Risk Managemen...

    39 Minutes Later
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    Michelle |Clinical Educator, Medical Writer, Legal

    I have been an RN for over 18 years with cross-training in perioperative, rehab and education. I hol...

    46 Minutes Later
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    Julia |healthcare

    I have run 100 million dollar corps, I understand *****liance and nursing roles, being a l...

    1.3 Hours Later
+24 Other Responses
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Clinical Laboratory Improvement Amendments

Looking for a consultant knowledgeable in clinical laboratory improvement amendments (clia). Expert should be able to guide laboratory in all aspects of clia compliance. Preferably located in the mid-west united states but open to the possibility of a consultant elsewhere within the us.

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    Ahmer |Founder and Principal Consultant

    I have worked in CLIA registered labs and have developed test kits for CLIA Labs. I am available to ...

    2.4 Hours Later
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    Michael |

    I am not knowledgable in this area....

    4.4 Hours Later
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    Robert |Owner, & Principal

    I own a consulting company that specializes in CLIA lab compliance. I am a Medical Technologist and ...

    6.3 Hours Later
+12 Other Responses
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