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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 Skincare Inquiries

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Pharmaceutical Products Deformulation

Hi there. I am looking for experts in deformulation in particular skincare products. I would also like to find someone who can analyse and quantify ingredients within the formulation?

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    Eric |Owner

    I have over 45 yrs experience in *****lopment in skin care, antiperspirants, hair care; a...

    1.2 Hours Later
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    Kalidas |Pharmaceutical Product Development Consu

    I can help you. I have 20 years experience in this area. For more *****se visit ExquisS...

    1.7 Hours Later
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    Ronald |Director of Research and Development/Tec

    You need this product reverse engineered. Please contact me @ *****...

    1.8 Hours Later
+7 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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    Clinical Trial Logistics

    Please let me know if you would like to provide consultation for the scope mentioned below we are looking for experts in clinical trial samples logistics (global) who can comment on the below mentioned points 1) market scenario (key vendors, market trends etc.,) in transport and warehousing for clinical trial samples and ancillary materials) 2) industry best practices in sourcing - sourcing best practices in transport and warehousing of clinical trials samples - cost components break-up, cost drivers - negotiation levers please note that this is only a high level scope and we will share a detailed questionnaire after the initial introductory call

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      Vadim |Senior Director, Clincal Research

      Yes, I can provide the ***** are looking for: for the last 15 years I was in charge of ven...

      43 Minutes Later
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      Deborah |Consultant

      I would be very interested in assisting this client....

      47 Minutes Later
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      Eugene |Scientific Director

      Hello. I'm Director of CRO. Can help you....

      1 Hour Later
    +11 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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    Clinical Biochemistry

    I'm looking for a biochemist who is mostly into cosmetics from body lotions to face creams and topical medication

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      Sivakumar |Associate Professor

      Interested....

      27 Minutes Later
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      Natalya |CEO

      Conduct research in this field and will be glad to contribute expertise...

      31 Minutes Later
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      Moses |Vice President

      Hi, I am a biochemist by training and I am an expert in several biochemical techniques. I have a s...

      14.6 Hours Later
    +5 Other Responses
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    Clinical Development Patient Recruitment

    We are looking for a clinical development patient recruitment expert who can help us validate some data about the industry. I have the cost components, cost break down, cost drivers and % budget allocation for patient recruitment & retention. Can this be validated and corrected if not right?

      +undefined 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
      +19 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 |Director of National Accounts

        I am not knowledgable in this area....

        4.4 Hours Later
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        Robert |Owner, Principal Consultant

        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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      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 |Director of Clinical Trials

        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 Trials + Data

      We are looking for experts in "clinical trials + data" to provide commentary and insights towards a startup that developed a data exploration platform that empowers critical insights to improve the accuracy and efficiency of research decisions. 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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        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 Management Consultant

          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 Research Regulatory Service

        • study objective: to assess the clinical research consulting space with special emphasis on independent review board (irb) services. The aim is to understand the dynamics in the service/product offerings (regulatory compliance, medical writing, strategic affairs, electronic consent manager, meeting scheduler etc.). In addition, we would also like to understand the market overview of irb services comprising of market size, recent trends, drivers, barriers, etc. Focus would be to understand the customer needs, competitive landscape, pricing and market landscape for irb consulting services (regulatory compliance, medical writing, strategic affairs etc.). • following are some of the key questions: o what are the different services offered under regulatory consulting in clinical research? O who are the key users / customers of regulatory consulting services? O what are the needs for these services of different customers o what are the factors that influence the customer’s purchase decision of consulting services / products? O who are the top players providing consulting services and what is their market share? O what are the billable rates charged on an hourly basis by the companies? O why, if at all, do the rates differ across various services? O are there different rates for different customer types? What are the reasons? O how is the pricing structured for software products such as electronic consent form, meeting scheduler etc.? o what are the key market trends, growth drivers and barriers to growth etc.? o where are the key opportunities within the regulatory consulting market? Preferred expert should meet the following criteria: o location: us o industry experience of 15+ years in the clinical research industry o worked in coordinating clinical trials, device trails and observational studies, regulatory & irb submission, recruitment, data collection and input, source documentation creation, and overseeing good clinical practices (gcp) and ich guidelines o understanding of clinical studies to ensure compliance with ich/gcp guidelines and federal regulations o knowledge of regulatory consulting services as well as software offerings specific to clinical trial / research o understanding of purchase process and pricing structure of consulting services

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          Larry |Principal Consultant

          I am a former FDA official and an expert on the ***** clinical trials. I also have experien...

          2 Hours Later
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          Juan |Sr and Scientific Director Translational

          I have more than 20 years in drug development and about 10 of them in clinical development. I have b...

          3.4 Hours Later
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          Pamela |Owner/Consultant

          I have over 30 years in Clinical Research experience, as a Director of Research and *****gement,...

          16.8 Hours Later
        +12 Other Responses
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