Clinical Research Associate I - FSO

Actively Reviewing the Applications

Fortrea

Bengaluru Full-Time 1–2 years

Posted 2 days ago • Apply by June 11, 2026

Job Description

What You Will Do

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

You Will Be Responsible For (but Not Only)

All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
All aspects of site management as prescribed in the project plans
General On-Site Monitoring

Requirements

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
1-3 years of Clinical Monitoring experience

Experience (Minimum Required)

Six (6) months experience in a related role (e.g., site management, in-house CRA, study coordinator, research nurse, etc.).
Basic understanding of Regulatory Guidelines.
Ability to work within a project team.
Good planning, organization, and problem-solving skills.
Good computer skills with good working knowledge of a range of computer packages.
Works efficiently and effectively in a matrix environment.
Valid Driver's License.

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