Mohamed Salman Faris Clinical research
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Clinical Research professional with over 10 years of experience across Clinical Trial Management, Trial Master File (TMF) operations, and Clinical Research Associate (CRA) roles. Experienced in end-to-end clinical trial processes, including study start-up, site management, TMF quality oversight, document compliance, and regulatory inspections readiness.
Currently working as a TMF Specialist at ICON, with prior hands-on experience as a CRA, managing site monitoring activities, ensuring protocol adherence, data integrity, and GCP compliance. Demonstrated ability to work in global clinical trials, collaborate cross-functionally, and maintain high quality standards under tight timelines.
Known for strong attention to detail, audit readiness mindset, regulatory knowledge, and problem-solving skills. Actively seeking opportunities to further grow in CRA/clinical operations roles, leveraging both monitoring and TMF expertise to support successful trial execution.

Subjects

  • Clinical Research Beginner-Expert

  • Clinical Research regulations Beginner-Expert

Experience

No experience mentioned.

Education

  • Clinical research and Regulatory Affair (Nov, 2014–Nov, 2015) from Sikkim Manipal University Distance Education, Surat

Fee details

    ₹500/hour (US$5.26/hour)

    Vary depend on syllabus and duration

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