Senior Clinical Research Associate - Oncology (US, Midwest)

Worldwide Clinical Trials Holdings, Inc.; Illinois; Híbrido; USD 97.000 - 193.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials Holdings, Inc. seeks a Senior Clinical Research Associate to support sites across the Midwest from a home-based role. You will travel regionally to monitor studies, drive data quality, and ensure compliance with protocols and regulations.

The ideal candidate has 5+ years as a regional traveling CRA and at least 2 years of oncology trial monitoring experience, with strong site-management skills. Competitive salary and benefits provided.

Formación

• Bachelor's Degree or Nursing Degree with 5+ years as regional traveling CRA.
• 2 years of Oncology trial monitoring experience.
• Willingness to travel within the region; 8–10 days per month.

Responsabilidades

• Manage clinical activities at investigative sites in Worldwide trials.
• Identify and assess potential sites to support study execution.
• Coordinate start-up activities and support contracts/budgets.
• Conduct monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site staff on protocol, data collection, and safety reporting.
• Monitor site performance and support study maintenance.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Collaborate with sites and study teams to drive data quality and safety.
• Support site closeout activities and ensure study requirements are met.

Conocimientos

Senior CRA experience

Site monitoring

Regulatory knowledge

Educación

Bachelor's Degree

Nursing Degree

Descripción del empleo

Make an Impact as a Senior CRA at Worldwide

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.

Where You'll Work

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

What You'll Do

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Identify and assess potential research sites to support successful study execution.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs),Interim Monitoring Visits (IMVs) and Closeout Visits (COVs).
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.
• Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

What You'll Bring

• Bachelor's Degree or a Nursing Degree, along with 5+ years as a regional, traveling Clinical Research Associate.
• 2 years of required experience monitoring Oncology 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 requirement.

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.

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.

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.

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.