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Clinical Trial Coordinator Jobs in Mumbai - PPD

CW
Clinical Trial Coordinator
PPD
PPD
Last Date 15 Jan 2021
This Job is Expired

PPD - Job Details

Date of posting: 15 Nov 20
  • According to the specific role (Central or Local),coordinates, oversees and
    completes functions on assigned trials activities detailed on the task matrix.
    • Performs department, Internal, Country and Investigator file reviews as assigned
    and documents findings in appropriate system.
    • Ensures allocated tasks are performed on time, within budget and to a high quality
    standard. Proactively communicates any risks to project leads.
    • Supports the maintenance of study specific documentation and systems including
    but not limited to: study team lists, tracking of project specific training requirements,

    system access management, and tracking of project level activity plans in appropriate

    system.
    • Provides system support (i.e. GoBalto & eTMF).
    • Supports RBM activities.
    • Performs administrative tasks on assigned trials including but not limited to: timely
    processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews,

    performing mass mailings and communications as needed, providing documents and

    reports to internal team members.
    • Supports scheduling of client and/or internal meetings.
    • Reviews and tracks local regulatory documents.
    • Transmits documents to client and centralized IRB/IEC.
    • Analyzes and reconciles study metrics and findings reports. Assists with
    clarification and resolution of findings related to site documentation.
    • Maintains vendor trackers.
    • Assists with coordination, compilation and distribution of Investigator Site File
    (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
    • Assists with study-specific translation materials and translation QC upon request.
    High / Secondary school diploma or equivalent and relevant formal academic / vocational

    qualification.

    Bachelor's degree preferred.

    Previous experience that provides the knowledge, skills, and abilities to perform the job

    (comparable to 0 to 1 year).

    In some cases an equivalency, consisting of a combination of appropriate education,

    training and/or directly related experience, will be considered sufficient for an

    individual to meet the requirements of the role.

    Knowledge, Skills And Abilities
    • Ability to work in a team or independently as required
    • Good organizational skills and strong attention to detail, with proven ability to handle
    multiple tasks efficiently and effectively
    • Demonstrated ability to effectively analyze project-specific data/systems to ensure
    accuracy and efficiency
    • Strong customer focus
    • Flexibility to reprioritize workload to meet changing project timelines
    • Demonstrated ability to attain and maintain a good working knowledge of applicable
    Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for

    all non-clinical/clinical aspects of project implementation, execution and closeout
    • Good English language and grammar skills and proficient local language skills as
    needed
    • Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and
    ability to obtain knowledge and master all clinical trial database systems
    • Ability to successfully complete PPD clinical training program
    • Self-motivated, positive attitude and good interpersonal skills
    Job: *Clinical Monitoring

    Organization: *IN BU

    Title: Clinical Trial Coordinator - L (12 month Contract)

    Location: IN-IN-Mumbai-Mumbai IN Fulcrum
  • Job Summary

    Job Type : Full Time
    Job Role : HR / Admin
    Job Category : Diploma,Recruitment
    Hiring Process : Face to Face Interview
    Who can apply : Freshers and Experienced (0 to 3 yrs )

    About PPD

    PPD
    This Job is Expired
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