Clinical Research Associate II - Oncology (US)

Worldwide Clinical Trials Limited spółka z ograniczoną odpowiedzialnością; North Carolina; Híbrido; USD 80.000 - 159.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Clinical Research Associate II to ensure high‑quality, compliant clinical studies. You will oversee site qualification, initiation, monitoring, and close‑out activities, partnering with investigators as we advance important research programs.

This home‑based position supports US sites; travel is expected 8–10 days per month, with regional focus. You will train site personnel, manage data quality, and ensure regulatory compliance throughout the study

Formación

• Requires monitoring clinical trials experience.
• Strong knowledge of clinical trial processes and site management.
• Willingness to travel regionally to US sites 8–10 days per month.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close‑out visits per protocol and GCP.
• Evaluate site feasibility and readiness for trial execution.
• Maintain essential regulatory and study documentation for inspection readiness.
• Train and support site personnel on protocol requirements and data quality.
• Verify source data and ensure safety and data integrity.
• Collaborate with sites to resolve data queries and support timely deliverables.
• Monitor investigational product accountability and site files.
• Prepare visit reports for Trial Master File updates.
• Contribute to protocol/CRF/monitoring plan development as needed.

Conocimientos

Site management

Regulatory knowledge

GCP/compliance

Educación

Bachelor’s Degree or Nursing Degree

Descripción del empleo

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.

Make an Impact as a Clinical Research Associate II at Worldwide

As a Clinical Research Associate II, you’ll play a critical role in ensuring clinical studies are conducted to the highest standards of quality, compliance, and patient safety. Your work will directly support the successful delivery of clinical research by partnering with investigative sites and study teams throughout the study lifecycle. In this role, you’ll take ownership of site qualification, initiation, monitoring, management, and close‑out activities while helping ensure accurate, timely, and reliable study data. You’ll serve as a trusted resource for site personnel, providing guidance, training, and support to promote protocol adherence and regulatory compliance. Working across multiple stakeholders, you’ll contribute to the success of clinical trials by driving data quality, supporting safety reporting, and maintaining strong site relationships that help advance important research programs.

Where You'll Work

This is a home‑based Clinical Research Associate role supporting sites across the United States. 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 United States. Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

What You'll Do

• Conduct site qualification, initiation, monitoring, and close‑out visits in accordance with study protocols, GCP requirements, and applicable regulations.
• Evaluate site feasibility and readiness to support successful study execution.
• Review and maintain essential regulatory, ethics, and study documentation to ensure compliance and inspection readiness.
• Train and support site personnel on protocol requirements, study procedures, and data quality expectations.
• Verify source documentation and review study data to ensure accuracy, completeness, and protection of patient safety.
• Partner with sites to resolve data queries, maintain investigator files, and support timely study deliverables.
• Monitor investigational product accountability, including receipt, storage, return, or destruction activities.
• Prepare detailed visit reports and provide updates for inclusion in the Trial Master File.
• Collaborate with study teams and contribute expertise to protocol, CRF, and monitoring plan development when requested.

What You'll Bring

• Bachelor’s Degree or a Nursing Degree, along with 2+ years as a regional, traveling Clinical Research Associate.
• Required experience monitoring clinical trials.
• Requires travel within the specified region; 8 – 10 DOS monthly.
• Experience in full‑service monitoring preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Salary and Benefits

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 - $79,500.00 - $158,500.00. The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it is 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. 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.