Senior Clinical Research Associate-- CNS​/Psychiatry - Southeast

Who we areWe’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.

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.

Join us!

Make an Impact as a Clinical Research Associate at Worldwide As a Clinical Research Associate (CRA), you’ll play a key role in advancing clinical research by managing site activities throughout the study lifecycle and helping ensure high-quality, compliant trial delivery.

You’ll work across studies from site identification and start-up through maintenance and close-out, partnering closely with investigative sites and study teams. Your experience in Psychiatry will be especially important as you guide sites, support effective data collection, and help protect patient safety.

You’ll join a collaborative Clinical Operations environment with regular coaching conversations, professional development support, and a career path that can lead to Clinical Trial Manager opportunities.

Where You'll Work This is a home-based Clinical Research Associate role supporting sites across the Southeast. 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 in the Southeast. Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

What You'll DoManage research activities at investigative sites participating in Worldwide’s clinical research projects.

Support sites throughout the full study lifecycle, from site identification and start-up through study maintenance and close-out.

Coordinate study start-up activities, including collecting required regulatory documentation and supporting contract and budget negotiations.

Conduct Study Initiation Visits (SIVs) and train sites on accurate data collection and safety-event reporting.

Manage ongoing site activities, primarily remotely, while maintaining effective communication and oversight.

Ensure sites comply with informed consent requirements, safety reporting expectations, and applicable regulatory requirements.

Partner with site teams to support high-quality study conduct and successful clinical trial delivery.

What You'll BringA four-year university degree or Nursing Degree.
5+ years of experience as a Clinical Research Associate.

Experience in Psychiatry required.

Experience in full-service monitoring PREFERRED.Excellent interpersonal, organizational, and communication skills, with strong attention to detail.

Ability to work effectively with little or no supervision.

Proficiency in Microsoft Office, CTMS, and EDC…