Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)

Worldwide Clinical Trials

Job Overview

Location

2 Locations

Job Type

Full-time

Full Job Description

📋 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.
• Join us!
• 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 Rare CNS is required.
• Candidates must reside in the Southeastern or Mid-Atlantic United States.
• Willingness to travel regionally required.

🎯 Requirements

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Experience in Rare CNS is required
• Candidates must reside in the Southeastern or Mid-Atlantic United States
• 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

Senior

Remote

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Worldwide Clinical Trials

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About Worldwide Clinical Trials

Worldwide Clinical Trials is a full-service contract research organization (CRO) specializing in Phase I-IV clinical trials across therapeutic areas including neuroscience, oncology, cardiovascular, immunology, and infectious diseases. Headquartered in Durham, North Carolina, the company provides end-to-end solutions for pharmaceutical, biotechnology, and medical device clients, encompassing clinical development, site management, data analytics, regulatory affairs, and patient recruitment. With a global footprint spanning North America, Europe, Asia-Pacific, and Latin America, Worldwide Clinical Trials leverages technology-driven approaches and a patient-centric model to accelerate drug development. The company emphasizes scientific rigor, operational excellence, and innovation in delivering tailored clinical trial services that support clients from early-phase research through post-marketing surveillance.

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