Senior Clinical Research Associate - CNS - Southeast (Remote)

Worldwide Clinical Trials; South Carolina; Presencial; USD 97.000 - 193.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to manage research activities at participating sites and support end-to-end study processes. You will work across CNS, Rare Disease, and other therapeutic areas, with regional travel in the southeastern United States.

Qualified candidates have 5+ years as a CRA, a 4-year degree or nursing degree, and experience with CNS or Rare Diseases.

Formación

• 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.

Responsabilidades

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Identify sites, perform start-up activities, support contract and budget negotiations, train sites on data collection.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informing consent, reporting safety events, and regulatory requirements via remote site management.

Conocimientos

Interpersonal communication

Oral communication

Written communication

Organizational skills

Independent work

Microsoft Office

CTMS

EDC systems

Educación

Bachelors degree or Nursing degree

Herramientas

CTMS

EDC systems

Descripción del empleo

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.

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. 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.

What You Will Do

• 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.

What You Will Bring To The Role

• 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.

Your Experience

• 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.

Compensation & Benefits

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace. The salary range for this position is $97,000.00 – $193,000.00 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.