Senior Clinical Research Associate- CNS - (Mid Atlantic)

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

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 Mid-Atlantic . 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 Do

• Manage 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 Bring

• A 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 systems.
• Proficiency in English, including strong oral and written communication skills.

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do.  Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

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 know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. 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.

About Us

This is who we are.

We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever.

We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.