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    FO

    Fortrea

    Clinical Research

    Associate Validator II

    Bangalore, IndiaRemoteFull-time2–4 yrs experiencePosted 2w ago
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    Job description

    Job Overview:

    Serve as a member of the project team with primary responsibility for all documentation requirements in support of Global EDC Solutions tasks to include receiving and logging-in and scanning contractual and validation documentation. Assist project teams with validation tasks as requested, i.e., with the creation, production, printing and tracking of study documentation and controlled documents.

    Summary of Responsibilities:

    • Serves as a member of the project team with primary responsibilities for all documentation, requirements to support global EDC solutions tasks.
    • Assist project teams with validation tasks as requested.
    • Assist with creation, production, printing and tracking of study documents and other controlled documents as needed.
    • Create and Execute validation test scripts as requested and document the test results.
    • Ensure quality of work.
    • Prioritize workload to meet specified completion dates.
    • Assist with the maintenance of validation metrics.
    • Carry out all activities according to Fortrea Standard Operation Procedures (SOPs) and project specific conventions within the framework of Quality Management and Good Clinical Practice (GCP)/ICH guidelines.
    • Maintain accurate records of all work performed.
    • Perform other duties as assigned by management.
    • Assist with special projects as designated.
    • And all other duties as needed or assigned.

    Qualifications (Minimum Required):

    • University / college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution.
    • Fluent in English, both written and verbal.

    Experience (Minimum Required):

    • 2–4 years of experience in CDM and EDC testing, with hands-on expertise in Rave and Veeva.
    • A neat, methodical, and thorough approach to the work with an emphasis on attention to detail.
    • Good concentration skills are required to meet the consistently high standards expected.
    • Self-motivation with the ability to work under pressure to meet demanding deadlines.
    • Effective communication skills and the ability to work as part of a team.

    Preferred Qualifications Include:

    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Physical Demands/Work Environment:

    • Remote-Based, as requested by the line manager
    • Work Timings: Should be flexible to accommodate shift-based working hours.

    Learn more about our EEO & Accommodations request here.

    Job details are sourced from the employer's original posting.

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    About the company

    Fortrea

    Fortrea is a company that provides clinical trial and research services.

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    Industry
    Clinical Research
    Open roles
    215

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