CRA II - Device Trials | 25% Travel

Abbott

United States

On-site

USD 82,000 - 141,000

Full time

4 days ago

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Job summary

Abbott is a global healthcare leader seeking a Clinical Research Associate II to support the execution and management of clinical studies across medical device and diagnostic programs. You will conduct site visits, assist in study startup, and ensure regulatory and quality standards are met.

The role requires 5+ years in clinical research and 2+ years in site monitoring, with 30–50% travel. Join Abbott and contribute to groundbreaking healthcare initiatives while benefiting from global exposure,

Qualifications

B.S. degree in life sciences or equivalent with minimum 5 years of clinical research experience.
Must have 2+ years of relevant experience in site monitoring.
Experience in conducting medical device and/or in-vitro diagnostics studies preferred; pharmaceutical background may also be considered.
Must be able to travel 30-50%.

Responsibilities

The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies, from concept to clinical study report per timelines and quality standards.
Conduct single or multi-center medical device clinical studies and perform study site visits (SQV, SIV, IMV, COV).
Participate in study start up activities and manage device shipping and accountability.
Maintain and audit Trial Master File to ensure inspection readiness.
Communicate study status to management and ensure delivery within budgets and timelines.