drjobs Senior Clinical Research Associate I (SCRA1), FSP model

Senior Clinical Research Associate I (SCRA1), FSP model

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1 Vacancy
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Job Location drjobs

Kuala Lumpur - Malaysia

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Overview:

The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as leader for projects of limited scope as assigned. Assume line management responsibilities as assigned. Act in the project role of a Local Project Coordinator or Lead CRA as assigned.

    Summary of Responsibilities:

    • Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned.

    • Responsible for all aspects of site management as prescribed in the project plans.

    Qualifications (Minimum Required):

    • University or college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution nursing certification medical or laboratory technology.

    • In lieu of the above education requirement candidates with a minimum of 3 years relevant clinical research experience in pharmaceutical or CRO industries will be considered.

    • Thorough knowledge of regulatory requirements including a basic understanding of regulatory requirements in other countries.

    • Thorough understanding of the drug development process.

    • Fluent in local office language and in English both written and verbal.

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

    Experience (Minimum Required):

    • Typically Three (3) years of clinical onsite monitoring experience.

    • Have a full understanding of Serious Adverse Event (SAE) reporting process production on reports narratives and follow up of SAEs.

    • Advanced site monitoring skills.

    • Advanced study site management skills.

    • Advanced registry administration skills.

    • Ability to work with minimal supervision.

    • Valid Drivers License.

    Physical Demands/Work Environment:

    • Travel requirements: 60-80%

    Learn more about our EEO & Accommodations request here.


    Required Experience:

    Senior IC

    Employment Type

    Full-Time

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