Make an Impact as a Clinical Research Associate at Worldwide
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 closeout. 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.
Where You'll Work
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.
What You'll Do
- 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.
What You'll Bring
- 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 travel regionally.
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 ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
