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

Role overview

Qualifications

  • A four-year university degree or Nursing Degree
  • 5+ years of experience as a Clinical Research Associate
  • Experience in Psychiatry required
  • Excellent interpersonal, organizational, and communication skills

Responsibilities

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

Key facts

Hard skills

Other skills

  • Communication
  • Organizational Skills
  • Microsoft Office
  • Detail Oriented
  • Social Skills

About the company

Worldwide Clinical Trials logo

Worldwide Clinical Trials

Contract Research Organizations (CRO)

About Worldwide Clinical Trials  Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

Who we are

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.

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 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.

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 - $193,000.00


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.

We love knowing that someone is going to have a better life because of the work we do. 

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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