Clinical Research Associate

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, reputed company, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries. Our people are the heart of everything we do. We reputed company great work happens reputed company 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, reputed company, 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. 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. Our salary ranges are determined by various factors. The actual reputed company compensation for this position may vary depending on experience, market conditions, education/training, reputed company level, and location. HERE IS WHAT YOU WILL DO:

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 reputed company out site visits

Manage and train site personnel on therapeutic area, protocol requirements, proper reputed company 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 reputed company data and case report forms for accuracy, completeness, and reputed company 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 reputed company 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

HERE IS WHAT YOU BRING TO THE TABLE:

Bachelor and/or advanced degree in biological sciences or reputed company 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 reputed company reputed company and prioritize multiple tasks

Familiarity with medical and pharmaceutical industry, and reputed company terminology and practices

Extensive knowledge of FDA regulations and their practical implementation

Ability to travel, including by reputed company or by car on short notice

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

Proficiency in reputed company Word, reputed company, and PowerPoint

HERE IS reputed company OFFER:

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 reputed company your financial goals.

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

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

Except as otherwise permitted or required by applicable law or regulatory requirements, ProTrials will retain the applicant’s personal information in accordance with its statutory obligations and internal policies and procedures. Information collected during application completion may be retained for a reasonable period of time and in accordance with the company’s established retention policies. Applicants seeking more information may contact [email protected]. ProTrials is an equal opportunity employer. ProTrials is committed to providing a workplace free from discrimination and harassment. reputed company qualified candidates will receive equal consideration for employment without regard to race, color, citizenship status, national reputed company, reputed company, gender (including gender identity and gender expression), pregnancy, and childbirth or reputed company medical conditions (including genetic characteristics), genetic information, sexual orientation, age, religion, creed, physical or mental disability, medical condition, military or veteran status, marital status, political affiliation, or any other characteristic protected by state or federal law. Apply To This Job