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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 Pediatric Pulmonary Medicine Inquiries

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Copd Drugs

I am working together with an institutional investor who is looking into the copd (chronic obstructive pulmonary disease) drug space. He would like to speak with people at pharma companies who could can speak to the current sales trends.

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    Md. Sadique |CEO and President

    Hi, Thank you for your query. To answer this, I will say yes. We bring diversified expertise in Hea...

    1.6 Hours Later
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    Nikolina |Regulatory Affairs Manager

    I am offering You consultancy help in establishing medicinal clinical presence on Macedonian market...

    8.8 Hours Later
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    marco |European Sales and Marketing Director

    Hello, I am a sales and marketing consultant and I am working with several pharma companies as a con...

    8.9 Hours Later
+7 Other Responses
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Sports Medicine Center

I would like to start a sports medicine center along with physical rehablitation center in pakistan . Aim is to treat all sportsmen within the country and provide rehab + fitness services to all general patients as well . This center will provide education and treatment .  

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    Claude |Owner/Consultant

    Have vast experience in Sports medicine & *****line, individual center or branches, medica...

    3.3 Hours Later
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    Fulvio |Managing Director

    My company is ficused on Human motion. We have a wide experience about ***** run sports medicin...

    3.6 Hours Later
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    Khurram |Director

    I am from Pakistan, have been practicing physical medicine and sports medicine for past > 10 years....

    4.3 Hours Later
+12 Other Responses
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Regenerative Medicine Risk Assessment

Dear experts, i am writing on behalf of a consulting firm that conducts expert interviews in support of industry-wide studies for many of the world's fortune 1000 companies. We are an authorized zintro partner. For a current intriguing study on global stakeholder reactions and risk assessment in regenerative medicine, we are seeking to speak with experts from various groups who could help us understand their perspective on regenerative medicine from an ethical, religious, legislative or social standpoint. We are interested in their opinion around associated challenges in r&d and commercialization of regenerative medicine and future trend and perception of such technology. We are targeting to speak with experts from one or more of the following groups related to regenerative medicine: 1. Large media groups (e.G. Bbc) 2. Patient groups (e.G. London regenerative medicine network) 3. Payor associations / financial support groups / ngos (e.G. Cancer financial assistance coalition, chronic disease fund, patient access network foundation, etc.) 4. Religious groups & associations (e.G. Muslim jewish forum, religious education group, st. John neumann roman catholic church, etc.) 5. Government organizations (e.G. National health service in the uk, departments of health) please note that we are only seeking to speak with experts from either the us or the eu5 markets (france, germany, uk, italy and spain), at this stage. We are only interested in personal opinions and are not interested in any confidential information. Our practice is to keep your identity anonymous, as well as that of our client. We are scheduling 45-60 minute discussions with experts ideally this week (before june 14th), or early next, and are happy to provide a flexible usd 250 compensation for each interview. Please note that we are handling the standard zintro fee separately, hence the expert is not involved in paying this. If you kindly let me know your contact details (email, phone/skype), i could provide more specifics on the study and standard process. We would welcome any referrals to other relevant experts as well. Best regards, lou senior specialist, delivery & expert community

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    Austin |MD/CEO

    I am a clinician expert....

    47 Minutes Later
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    Nikolaos |Associate Professor of Biological Chemi

    Hi, I am highly interested in providing the requested consultancy. My (USA) phone is ***** Sin...

    3.8 Hours Later
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    Abdulraheem |Researcher

    Dear Lou I am a PhD in Molecular Biology and I am knowledgeable of Islamic laws as a Muslim my self....

    12.7 Hours Later
+17 Other Responses
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Sleep Technologies & Medicine

I am conducting research to better understand emerging trends and technologies related to sleep. If you qualify for any of the below descriptions, please contact me to discuss scheduling an interview. 1. Payors- experience in sleep medicine 2. Industry consultant- specialty in future technologies and emerging trends in sleep 3. Physician- specialty in sleep medicine 4. Professional association board member- specialty in sleep trends and technologies

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    Lev |Chief Medical Officer

    I am board certified in sleep medicine. what's the honorarium amount and length of call?...

    31 Minutes Later
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    Steve |Senior Vice President

    ***** 8:38AM Good morning, I am a Bedding & Sleep Industry consultant with manufacturing, retai...

    41 Minutes Later
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    Ron |CEO, Americas

    Board member of Sleep Safe Drivers and California Sleep Disorder Centers Have managed and operated o...

    44 Minutes Later
+43 Other Responses
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Clinical Trials Management

This is a 12 month contract opportunity in california: clinical trial manager/sr ctm - asthma overview: responsible for managing the full scope of proper study conduct including, but not limited too, protocol development to final report, regulatory filing and/or publications, coordinating cross functional efforts in the administration and progress of phase 1 to 4 clinical trials. Additional responsibilities include trial start-up, conduct, and close-out activities in order to achieve program objectives and goals. The incumbent will use professional concepts in accordance with company objectives to solve complex problems in creative and effective ways. May determine methods and procedures on new assignments. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Responsibilities: -lead clinical trial project execution for asthma programs to ensure that trial timelines, costs, and quality metrics are met. -serves as primary contact for functional area representatives in managing protocol execution. -manage the financial aspect of clinical trials to ensure accuracy and timeliness of service provider and site payments. -forecast and oversee clinical supplies, e.G. Study drug. -manage study milestones to ensure accurate tracking and reporting of study metrics. -oversee ongoing service provider management (e.G., cros, ivrs, central labs), including independent negotiation of scope of work, budgets, performance management, and issue resolution. -create and manage clinical trial budgets in collaboration with manager and the vice president of clinical operations. -may provide study-specific direction and mentoring to cras and ctas. -collaborate with clinical quality assurance to maintain quality standards in compliance with regulatory requirements/guidance’s and adherence to sops and ich/gcps; participate in ongoing process improvement initiatives. -manage adherence to ich/gcp/local regulations. -participate in clinical operations initiatives and programs. Qualifications: -bachelor’s degree with at least 5 to 8 years of cra experience for the manager level with at least 1 year of staff management experience. The senior manager level requires 10+ years of combined cra and ctm experience and 3 years direct staff management experience is required. -experience in inflammatory diseases, specifically asthma and/or chronic obstructive pulmonary disease (copd) is required. -experience developing trial plans including developing creative strategies for site monitoring, risk mitigation, trial budgets, site selection, and clinical supplies management. -extensive clinical research knowledge and cross-functional understanding of clinical trial methodology. -team oriented and collaborates effectively with the clinical operations study team, cross-functional team members, and external partners. -working knowledge of ms project for development and update of clinical study timelines. Contact us here on zintro for further details.

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    ALIYA |CTM, PM

    Is this in-house role? Could the ***** Russia be considered?...

    1.7 Hours Later
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    Terry |President

    I have extensive knowledge of the clinical trial process having held the position of Global Director...

    4.8 Hours Later
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    Nate |Research Manager

    Dear Sir: By training I am a *****iologist who has been a senior Medical Affairs/clinical...

    9.1 Hours Later
+17 Other Responses
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Alternative Medicine

Holistic alternative medicine for assisting someone with stage iv cancers in the lymph glands, colon (colostomy has been performed, bag in place), liver, pelvic wall

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    Norval |Chi Practitioner

    I am a non-local practitioner. All my sessions are done by serving as a proxy for you. No phone call...

    26 Minutes Later
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    Michael |Strategic Consultant

    Hello I saw your recent posting for an engagement regarding *****cine in the *****...

    50 Minutes Later
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    Jared |CEO

    I'd be interested to learn more about what you are looking for. If I can't help, I can refer you to ...

    52 Minutes Later
+5 Other Responses
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Personalized Medicine

I'm writing an article on this topic and am looking for more sources with expertise in personalized medicine, stakeholders and marketplace dynamics (e.G., cost-shifting to consumers, the recession, health reform, etc.). Is there a personalized medicine business model now? Is it working? If not, why not? What might a new business model look like?

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    Towia |Director of Genomics and Proteomics Cent

    I am the director of the Beth Israel Deaconess Medical Center Genomics and Proteomics Center and of ...

    19 Minutes Later
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    Michael |Consultant

    What is the scope of your article? Are you looking for experts outside the US?...

    35 Minutes Later
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    Paul |Physician, CEO, and Health Technology Co

    I'm a physicoan in *****tice in San Francisco with a business model that supports personalize...

    1 Hour Later
+27 Other Responses
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Personalized Medicine

Hello, we are interested in understanding better how sales force for leading pharma is changing in the face of personalised medicine revolution. Are reps co-promoting diagnostic testing? Who is training them in pm? How are they targeting docs? Interested in any large/mid size pharma with pm therapies with clear diagnostic strategy on market or in the pipeline. Thanks and have a good day.

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    Michael |CMSO , Chief Medical Strategies Officer

    Hi We presently have contracts that are both global and domestic (USA). We are also working with var...

    6.8 Hours Later
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    Kuldeepak |Director

    Thanks for your message. As a pharmaceutical medical device consultant & Ph.D. in pharmaceutics medi...

    7.5 Hours Later
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    Terry |President

    I have first hand experience with developing companion diagnostics for large Pharma in my previous p...

    9.3 Hours Later
+6 Other Responses
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Ayurvedic Medicine Formulations

I am in need of following ayurvedic drug formulations and herbal cosmetic formulations for ayurvedic factory unit in kolhapur, maharashtra. The details are as ayurvedic drug formulations sr. No. Name of disease form of medicine remark 1 heart tablet 2 kidney tablet 3 blood pressure tablet 4 diabetes tablet 5 anti stress tablet 6 detox tablet 7 lever tablet 8 lever liquid 9 cough and cold syrup 10 fever tablet 11 antiaging tablet 12 antiaging tonic herbal formulations sr. No. Type of product form 1 beauty cream paste 2 face wash paste 3 shampoo 4 soap our requirements for ayurvedic medicine formulations are 1. Formulations are proprietary in nature 2. Can be used for curative and preventive purpose 3. Contain minimum required ingredients only ( minimum ingredients formulations) 4. Bhasma, metals, poisonous materials, mercury and alcohol or self generating alcohol shall not be used in formulations 5. Specify binding agent and colour coating for tablet 6. Clearly specify ingredients percentage or quantity. 7. Expiry period is maximum three years. 8. Write in detail manufacturing procedure, therapeutic index, indication, contra indications and dosages. Kindly email me about time required for formulations and approximate estimate with clinical trial and without clinical trial thanks

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    Dr Vijayanand |Zintro Expert

    Hello I am Dr Vijayanand Pujari experienced in supplement formulation. Please see my profile Than...

    13.2 Hours Later
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    Ghale |Head

    Hi, I am a pharma project freelancer, please check my profile ...

    13.4 Hours Later
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    Vallal |Consultant

    first you got pay my fee on the portal to further ***** sought details. i shall make this ...

    13.7 Hours Later
+13 Other Responses
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Veterinary Medicine

I am in need of a doctor in veterinary medicine to serve as an expert witness in a veterinary malpractice case in miami, fl.

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    Jill |Consultant

    I am avaiIable, but I am near Athens, GA. I have 19.5 years of experience in small animal medicine....

    2.6 Hours Later
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    David |Veterinarian

    I have 36 years post-grad veterinary experience and have served as an expert witness in two trials i...

    2.8 Hours Later
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    Harold |CEO Glencroft Veterinary Hospital, Visit

    I am a veterinarian with over forty years of practice experience and also university professor...wha...

    18.7 Hours Later
+4 Other Responses
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Precision Medicine

We are looking for experts in "artificial intelligence driven precision medicine" to provide commentary and insights towards a startup that developed an open cloud platform that hosts ai driven precision medicine tools known as clinical classifiers. We are an angel investing platform dedicated to connecting deep-tech startups with angel investors. By deep-tech we mean startups founded on scientific breakthroughs and technological innovations that create lasting impact on mankind. As a participating expert* in this process, your involvement is limited to answering anywhere between 8-12 investor-submitted questions. This takes about 1 hour (+/-) . Once you are vetted, we send those questions via a web form for your responses. If your contribution is published, it will be view-able by potential investors in this startup, giving you an opportunity to make connections, socialize virtually, and gain bragging rights in a vibrant entrepreneurial and angel investing community. *at this point, we cannot guarantee any monetary reimbursement. You do get insights to new upcoming technologies in your field and a tremendous networking opportunity!

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    Victor |Professor of Computer Science

    Hello, I worked many years in bio-medical data analysis applying AI and Machine learning methods an...

    38 Minutes Later
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    Jaime |Full time Researcher Principal Investiga

    I'm interested please send the questions. Warm greetings!...

    3.8 Hours Later
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    Yury O. |Research Scientist

    Experienced in biomarker discovery and ***** machine learning algorithms for development...

    12.2 Hours Later
+14 Other Responses
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Nuclear Medicine

Need an expert witness on nuclear medicine shielding for a case in litigation cant afford a lot

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    Joe |Director Sales and Operations

    Hi, I received your inquiry into Nuclear Medicine, let me know what you have in mind!...

    2 Hours Later
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    AHAMAD |consultant

    i will help you...

    7.8 Days Later
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    Marie |Mid Central Region Ultrasound Sales Mana

    i thank you for the opportunity but do not feel this is the best fit for me.... Ultrasound and Echoc...

    9.8 Days Later
+6 Other Responses
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