Clinical Research Associate

Insight Global; United States; Remote; USD 55,000 - 65,000; Full time

Job summary

A leading company is seeking a Clinical Research Associate to support clinical studies for a Fortune-500 Medical Device client. This remote role involves significant travel, overseeing site operations, and ensuring regulatory compliance during clinical studies, requiring 3-10 years of experience and a relevant Bachelor's degree.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• 3-10 years of experience as a field-based Clinical Research Associate.
• Strong site management and data monitoring experience required.

Responsibilities

• Author study-specific Monitoring Plan aligned with clinical investigational plan.
• Train and manage clinical study sites ensuring compliance with regulatory requirements.

Skills

Site management

Data monitoring

Technical proficiency in Veeva eTMF

Ability to operate independently

Willingness to travel

Education

Bachelor's Degree in healthcare or science related field

Job description

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This range is provided by Insight Global. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$46.00/hr - $61.00/hr

Direct message the job poster from Insight Global

Insight Global is looking for a Clinical Research Associate to support one of our Fortune-500 Medical Device clients. The purpose of this position is to provide study monitoring for clinical studies conducted by the Urology Critical Care (UCC) business unit. The studies range from simulated use studies to complex studies that may include devices or drug/device combinations. The Clinical Research Associate serves as a study monitor for moderate to complex studies in compliance with Good Clinical Practices. A key focus of this role is overseeing site operations and proactively resolving any issues that arise during the course of the study. The Clinical Research Associate role encompasses responsibilities across both data management and on-site study oversight. This remote role includes regular travel—up to 50%—for site visits, check-ins, and related responsibilities. When not traveling, the position will be performed from a home-based office.

Responsibilities:

• Author study-specific Monitoring Plan aligned with clinical investigational plan

• Prepare, Contribute, Review and/or maintain study specific documentation and training materials

• Possess a working knowledge of the disease state and product(s) under investigation

• Effectively train and manage clinical study sites ensuring compliance with regulatory requirements and standards

Required Skills & Experience

3-10 years of experience as a field-based Clinical Research Associate in the medical device/pharmaceutical industry

Strong site management and data monitoring experience

Technical proficiency in Veeva eTMF (Data Management System)

Ability to work and operate independently

Willingness and ability to travel up to 50% of the time for business-related site visits and responsibilities

Bachelor's Degree in healthcare or science related field

Nice to Have Skills & Experience

Previous experience or familiarity with the Urology and Critical Care therapeutic area

Job Description

Insight Global is looking for a Clinical Research Associate to support one of our Fortune-500 Medical Device clients. The purpose of this position is to provide study monitoring for clinical studies conducted by the Urology Critical Care (UCC) business unit. The studies range from simulated use studies to complex studies that may include devices or drug/device combinations. The Clinical Research Associate serves as a study monitor for moderate to complex studies in compliance with Good Clinical Practices. A key focus of this role is overseeing site operations and proactively resolving any issues that arise during the course of the study. The Clinical Research Associate role encompasses responsibilities across both data management and on-site study oversight. This remote role includes regular travel—up to 50%—for site visits, check-ins, and related responsibilities. When not traveling, the position will be performed from a home-based office.

Responsibilities:

• Author study-specific Monitoring Plan aligned with clinical investigational plan

• Prepare, Contribute, Review and/or maintain study specific documentation and training materials

• Possess a working knowledge of the disease state and product(s) under investigation

• Effectively train and manage clinical study sites ensuring compliance with regulatory requirements and standards

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Administrative

• Industries

  Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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