
Senior Clinical Research Associate - Oncology/Rare Disease - Texas (Remote)
Job Overview
Location
Austin, Texas
Job Type
Full-time
Category
Product Management
Date Posted
July 10, 2026
Full Job Description
đź“‹ Description
- • We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
- • We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
- • Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
- • We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed.
- • We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.
- • At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
- • As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
- • Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it’s ingrained in our culture.
- • Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment.
- • In a CRA role, you’ll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
- • Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority.
- • We offer a clear career path and development that can lead to Clinical Trial Manager roles.
- • We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
- • We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial.
- • Experience a world of difference with us at Worldwide!
- • Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
- • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site’s activities during study maintenance, and closing down research activities at the sites once the study has concluded.
- • Conduct study initiation visits (SIVs).
- • While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.
- • Excellent interpersonal, oral, and written communication skills in English.
- • Superior organizational skills with attention to detail.
- • Ability to work with little or no supervision.
- • Proficiency in Microsoft Office, CTMS, and EDC Systems.
- • 5+ years of experience as a Clinical Research Associate.
- • 4-year university degree OR Nursing Degree.
- • Experience in Oncology and Rare Disease is required.
- • Candidates must reside in the Central United States, preferably Texas.
- • Willingness to travel regionally required.
🎯 Requirements
- • Excellent interpersonal, oral, and written communication skills in English.
- • Superior organizational skills with attention to detail.
- • Ability to work with little or no supervision.
- • Proficiency in Microsoft Office, CTMS, and EDC Systems.
- • 5+ years of experience as a Clinical Research Associate.
- • 4-year university degree OR Nursing Degree.
- • Experience in Oncology and Rare Disease is required.
- • Candidates must reside in the Central United States, preferably Texas.
- • Willingness to travel regionally required.
🏖️ Benefits
- • Salary range: $97,000.00 - $193,000.00.
- • Competitive benefits package depending on location.
- • Pay equity and transparency.
- • Compliance with all applicable labor laws.
Skills & Technologies
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About Worldwide Holdings Corporation
Worldwide Holdings Corporation is a diversified global enterprise engaged in the development, manufacturing, and marketing of a wide range of products and services. The company operates across various sectors, including technology, consumer goods, and industrial solutions, with a strong focus on innovation and sustainability. Worldwide Holdings Corporation is committed to delivering high-quality products and exceptional customer service, aiming to foster long-term relationships with its clients and stakeholders. The company's strategic vision involves expanding its global reach, investing in research and development, and adapting to evolving market demands to maintain a competitive edge in the international marketplace. Their mission is to create value through responsible business practices and a dedication to excellence.
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