Senior Clinical Research Associate - Oncology (US)

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 90,000 - 130,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior CRA to ensure high-quality clinical studies from site qualification through closeout. This home-based role supports sites across the United States, with travel required to investigator sites and collaboration with sponsors and global teams.

You will lead site management, ensure protocol adherence, regulatory compliance, and data quality, while guiding investigators and study teams to successful study delivery.

Qualifications

• Bachelor’s Degree or Nursing Degree required.
• 5+ years as a regional, traveling CRA.
• Experience monitoring Oncology trials.

Responsibilities

• Manage CRAs at investigative sites participating in Worldwide studies.
• Identify and assess potential research sites.
• Coordinate study start-up activities and regulatory documentation.
• Conduct monitoring visits: PSSV, SIV, IMV, COV.
• Train site personnel on protocol requirements and safety reporting.
• Monitor site performance and provide ongoing support.
• Ensure consent, safety reporting, and regulatory compliance.
• Collaborate with sites and study teams to drive data quality.

Skills

Oncology monitoring

Clinical trial oversight

Site management

Travel 8–10 days/mo

Regulatory compliance

Education

Bachelor’s Degree or Nursing Degree

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 Senior CRA at Worldwide

As a Senior CRA, you’ll play a critical role in ensuring clinical studies are conducted with the highest standards of quality, patient safety, and regulatory compliance. Your expertise will help drive the successful execution of studies from site qualification through closeout, supporting the delivery of reliable data that advances clinical research. In this role, you’ll serve as a trusted partner to investigative sites, study teams, and sponsors, building strong relationships while providing leadership, guidance, and oversight across clinical trial activities. You’ll have the opportunity to influence study success through proactive monitoring, site management, and collaboration with global teams. Your contributions will directly support high‑quality study delivery by ensuring protocol adherence, regulatory compliance, timely data collection, and effective site performance throughout the clinical trial lifecycle.

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 United States. Travelwillprimarilybe regional, with occasional travel to support sites inother locations as needed.

What You’ll Do

• Manage clinical research activities at investigative sites participating in Worldwideclinical 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 typesofmonitoring visits: Pre‑Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits(IMVs)andCloseoutVisits (COVs).
• Train site personnelon protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performanceandprovideongoing support throughout study maintenance activities.
• Ensure compliancewithinformed consent requirements, safety reporting obligations,and applicable regulatory standards.
• Partnerwithsitesandstudyteamsto drivedata quality, participant safety, and overall studysuccess.
• Supportsitecloseoutactivitiesandensurestudyrequirementsarecompletedattheconclusion of the trial.

What You’ll Bring

• Bachelor’sDegreeoraNursingDegree,alongwith5+ years as a regional, traveling Clinical Research Associate.
• Required experience monitoring Oncology clinical trials.
• Requires travel within the specified region;8–10DOSmonthlyExperienceinfull‑servicemonitoringpreferred.
• Strongknowledgeof clinical trial processes,sitemanagement,and regulatoryrequirements.

Salary

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 - $0.00 - $1,000,000.00. The salary range providedis intendedto give candidates anunderstandingofpotential earnings. Compensationwillfallwithinthe provided range, and it not a guaranteeofexactsalary. Thefinal salarywillbedeterminedbased onrelevantexperience,performance,education, and internalequity.

Benefits

In additiontobasesalary,we offera competitive benefits package depending on location. Weensure pay equity and transparency and complywithall applicablelabor laws. Salaryinformationwillbe discussed during the interviewprocess,andwe encouragecandidatesto inquireabout compensation at anystage.

Careers and Company

To viewour otherroles, checkoutourcareers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

About Us

This is whowe 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.