Senior Clinical Research Associate - CNS - Southeast; 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 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. 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 not just encouraged; it’s ingrained in our culture.

You will receive extensive support through regulatory submissions, TMF management, and in‑house CRAs for projects with heavy site‑management needs.

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Involved in all stages of the clinical study, including identifying potential sites, performing study start‑up activities, supporting the negotiation of contracts and budgets, training sites to collect data properly, reporting safety‑related events, managing site activities during study maintenance, and closing down research activities once the study has concluded.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informing consent, reporting safety‑related events, and adhering to all applicable regulatory requirements, primarily through remote site‑management efforts.

• 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 CNS required;
  Rare Disease preferred.
• Candidates must reside in the southeastern United States.
• Willingness to travel regionally required.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace. The salary range for this position is $97,000.00 – $ per annum. Compensation will be determined based on relevant experience, performance, education, and internal equity. In addition to a base salary, we offer a competitive benefits package. Salary information will be discussed during the interview process. We encourage candidates to inquire about compensation at any stage.