Senior Clinical Research Associate- CNS -Psychiatry - East Coast

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!

Make a meaningful impact on clinical research by managing site activities across Worldwide’s clinical studies. As a Clinical Research Associate, you’ll help ensure studies are conducted effectively, with a strong focus on quality, patient safety, and regulatory requirements. You’ll work across the clinical study lifecycle, from site identification and start‑up through study maintenance and close‑out. You’ll collaborate with sites and study teams while receiving support across regulatory submissions, TMF management, and site management activities.

You’ll also have regular coaching and development conversations with your Line Manager, with a clear career path that can lead to Clinical Trial Manager opportunities.

This is a home‑based Clinical Research Associate role supporting sites across the East Coast. Candidates must reside within the territory to effectively support site visits and study activities. You will collaborate with sites, sponsors, and global study teams while traveling to investigative sites approximately 8-10 days per month. To best support our sites, we’re seeking candidates who are based on the East Coast.

Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

• Manage research activities at investigative sites participating in Worldwide clinical research projects.
• Support sites throughout the clinical study lifecycle, from identification and start‑up through maintenance and closeout.
• Coordinate study start‑up activities, including collecting appropriate regulatory documents and supporting contract and budget negotiations.
• Conduct study initiation visits and train sites on accurate data collection and safety event reporting.
• Monitor site activities and help ensure compliance with informed consent, safety reporting, and applicable regulatory requirements.
• Partner with sites and study teams to address site management needs and support successful study delivery.

• Bachelor’s degree from a four‑year university or a Nursing Degree.
• 5+ years of experience as a Clinical Research Associate.
• Experience in Psychiatry.
• Experience in full‑service monitoring (PREFERRED).
• Excellent interpersonal, oral, and written communication skills, including proficiency in English.
• Strong organizational skills with excellent attention to detail and the ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Residence on the East Coast and willingness to…