Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects, predominantly registries and other types of non‑interventional/observational studies.
• Oversee all stages of the clinical study, including identifying potential sites, performing study start‑up activities such as collecting regulatory documents, supporting contract and budget negotiations, training sites for accurate data collection, and reporting any safety‑related events.
• Conduct site initiation visits (SIVs).
• Ensure compliance with informed consent requirements, reporting of safety events, and all applicable regulatory requirements.
• Manage site activity during study maintenance and conduct the closing of research activities once the study concludes.

Skills & Qualities

• 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.

Required Experience and Education

• 2+ years of experience as a Clinical Research Associate.
• 4‑year university degree or RN/BSN in Nursing.
• Willingness to travel.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. #J-18808-Ljbffr