Senior Clinical Research Associate - Oncology/Rare Disease - Texas (Remote)

Who we are

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.

Why Worldwide

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.

What Clinical Operations does at Worldwide

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.

What you will do

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Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects

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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

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Conduct study initiation visits (SIVs)

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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

What you will bring to the role

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Excellent interpersonal, oral, and written communication skills in English

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Superior organizational skills with attention to detail

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Ability to work with little or no supervision

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Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

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5+ years of experience as a Clinical Research Associate

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4‑year universitydegree OR Nursing Degree

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Experience in Oncology and Rare Disease is required

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Candidates must reside in the Central United States, preferably Texas

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Willingness to travel regionally required

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $97,000.00 - $193,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.