Senior Clinical Research Associate- CNS - (Mid Atlantic)

Worldwide; North Carolina; A distancia; USD 97.000 - 193.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for CNS studies, covering the Mid-Atlantic region. The role is home-based in the Southeast, with travel to investigative sites roughly 8-10 days per month and collaboration with sponsor teams to ensure high-quality trial delivery.

The ideal candidate will have a four-year degree or nursing degree, 5+ years of CRA experience, and experience in Psychiatry.

Formación

• 5+ years of CRA experience.
• Experience in Psychiatry required.
• Proficiency in English, including strong oral and written communication.
• Four-year university degree or Nursing Degree.

Responsabilidades

• 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.

Conocimientos

5+ years CRA experience

English proficiency

Educación

Four-year university degree or Nursing Degree

Herramientas

Microsoft Office

CTMS

EDC systems

Descripción del empleo

Senior Clinical Research Associate- CNS - (Mid Atlantic)We use cookies to improve your browsing experience and help us improve our websites. We have carefully selected third parties that use cookies to achieve purposes illustrated in the cookie policy. For more information. Read more about online privacy statement. By closing this banner or continuing to browse our website, you agree to our use of such cookies.https://www.worldwide.com/privacy-statement-terms-of-use/online-privacy-statement/# Discover a world of difference at Worldwide.## Senior Clinical Research Associate- CNS - (Mid Atlantic)Apply: Remote: Research Triangle Park, North Carolina: Full time: Posted Today: JR103269Join 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): United States of America - $97,000.00 - $193,000.00The 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**.**