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  2. Clinical research associate - Wikipedia

    en.wikipedia.org/wiki/Clinical_research_associate

    A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.

  3. Medical science liaison - Wikipedia

    en.wikipedia.org/wiki/Medical_science_liaison

    A medical science liaison (MSL) is a healthcare consulting professional who is employed by pharmaceutical, biotechnology, medical device, and managed care companies.Other job titles for medical science liaisons may include medical liaisons, clinical science liaisons, medical science managers, regional medical scientists, and regional medical directors.

  4. Syneos Health - Wikipedia

    en.wikipedia.org/wiki/Syneos_Health

    [20] [1] As of the end of 2022, the company's clinical services business contributed to 75% of its revenue and the commercial services contributed to the remaining 25%. [1] The company generated $4.42 billion in revenue in 2020, $5.21 billion in 2021, [19] and reported $5.39 billion in 2022. [1] Syneos Health employs about 28,000 people in 110 ...

  5. Contract research organization - Wikipedia

    en.wikipedia.org/wiki/Contract_research_organization

    The International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, a 2015 Swiss NGO of pharmaceutical companies and others, defined a contract research organization (CRO), specifically pertaining to clinical trials services as: [8]: 10 "A person or an organization (commercial, academic, or other) contracted by the sponsor to perform one or ...

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  7. Clinical data management - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management

    The clinical data manager plays a key role in the setup and conduct of a clinical trial. The data collected during a clinical trial form the basis of subsequent safety and efficacy analysis which in turn drive decision making on product development in the pharmaceutical industry.

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