Senior Clinical Research Associate - Rare CNS - Southeast

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 a global team of over 3,500+ experts, bright thinkers, dreamers and doers, and together, we are changing the way the world experiences CROs.

About Us

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 promotes 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.

About Clinical Operations

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), you will work 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 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.

Responsibilities

• Manage the research activities at sites participating in Worldwide’s clinical research projects
• Involvement in all stages of the clinical study, including identifying potential sites, performing study start-up activities (e.g., collecting regulatory documents, supporting contract and budget negotiations), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements (most site management performed remotely)

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

Qualifications

• 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 United States (Florida preferred)
• Willingness to travel regionally required

Pay

The salary range for this position is $97,000.00 - $193,000.00 annually. 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.