Clinical Research Associate

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HealthcareClinical Research AssociateLaboratory & Life SciencesClinical Researcher

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Quick Summary

Overview

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the…

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Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health.

We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence.

ABOUT THE JOB

The Clinical Research Associate plays a vital role in the Clinical Operations team. Through responsibilities like monitoring studies, reviewing data, and engaging with sites, the CRA will ensure the success of clinical trial operations and management.

Monitor clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit including qualification, initiation, interim, and close out site visits

Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion

Manage, prepare, send, track, and return investigational supplies at individual sites

Monitor and document investigational product dispensing, inventory, and reconciliation

Monitor and document laboratory sample storage and shipment

Monitor trial by reviewing and reporting on site enrollment and termination updates, monitoring visits, protocol deviations/exceptions, serious adverse events, and laboratory abnormalities

Review source data and case report forms for accuracy, completeness, and integrity of the data, and identify and resolve ongoing data issues

Review data queries and listings, and work with the study centers to resolve data discrepancies

Review regulatory documentation for accuracy and completeness, and support study centers with regulatory issues

Maintain complete and accurate study files and review files to ensure all appropriate documentation is present

Maintain consistent and timely contact with the study centers, investigators, coordinators, client personnel, and other individuals involved in clinical trials

Follow Good Documentation Practices, complete Visit Reports and site correspondence in accordance with SOPs

Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training

2 years of prior experience as a Clinical Research Associate preferred

Detail oriented

Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills

Flexibility with changing priorities

Ability to efficiently perform and prioritize multiple tasks

Familiarity with medical and pharmaceutical industry, and related terminology and practices

Extensive knowledge of FDA regulations and their practical implementation

Ability to travel, including by air or by car on short notice

A valid driver's license with access to a car with up-to-date car insurance

Proficiency in Microsoft Word, Excel, and PowerPoint

Your wellness matters to us – that’s why we provide full medical, dental, and vision insurance options for you and your family.

We know life doesn’t pause for work – we provide flexible PTO so you can take care of what matters, both personally and professionally.

You invest in your future – and so do we. Our 401(k) plan includes a company match to help you reach your financial goals.

At ProTrials, we are committed to your growth. Whether you’re looking to expand your skills or take the next step in your career, we provide the support and opportunities you need to keep moving forward.

We have the best coworkers, if we do say so ourselves.