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About the company KUR International is a global healthcare conglomerate with its Headquarters in Dallas, Texas; dedicated to furthering science, research, and human wellbeing. We

MAKE PROGRESS POSSIBLE

by delivering an advanced and seamless clinical experience for patients resulting in a superior healthcare outcome. KUR has subsidiary companies like KUR Research, UCC Trials, KUR Diagnostics, Vexillum & Atlas Essentials. KUR Research is a Fully Integrated Clinical Research Site Management Organization with a proven track record of success performing hundreds of clinical trials. Urgent Care Clinical Trials (UCCT) is the first Fully Integrated Clinical Research Site Management Organization dedicated specifically to the urgent care industry. Vexillum is a large geographically diverse infectious disease biobank. KUR Diagnostics provides various preventative care and screening programs. providing results which show patient's present health risks and helps physicians in developing an individualized care plan to reduce future risk of experiencing life-threatening issues. Atlas Essentials is the management organization for all KUR International Companies. Atlas India provides full administrative support and integrated infrastructure in support of all KUR's global teams.

Job Title:

Site Manager At KUR Research, we believe exceptional clinical research begins with exceptional leaders. We're seeking an experienced Site Manager to lead one of our growing Alabama research sites. This is more than a leadership role. It's an opportunity to build a high-performing team, shape operational strategy, strengthen sponsor relationships, and expand patient access to innovative therapies—all while partnering directly with executive leadership. If you're ready to build something meaningful instead of simply maintaining the status quo, we'd love to meet you. Why You'll Love This Opportunity? At KUR, leaders don't simply manage operations—they influence strategy. You'll have the opportunity to: Lead and grow an expanding clinical research site. Partner directly with executive leadership. Build and mentor a high-performing clinical research team. Influence operational strategy and site performance. Work with leading Sponsors and CROs. Drive patient enrollment and study success. Advance your career within a rapidly growing organization. Make a meaningful impact in your community. What You'll Lead Build High-Performing Teams Supervise and mentor clinical research staff, including investigators, coordinators, and laboratory personnel. Organize, prioritize, and schedule work assignments to ensure optimal study execution. Provide direction and support during subject screening and enrollment to achieve study targets. Recruit, onboard, train, and evaluate team members, including conducting interviews and performance reviews. Promote a positive, compliant, and collaborative workplace culture aligned with organizational values. Clinical Operations Oversee the conduct of all clinical trials in accordance with FDA regulations, ICH-GCP, and organizational SOPs. Ensure all personnel are trained on study protocols and assigned responsibilities prior to study activation. Monitor enrollment, retention, protocol adherence, and data quality. Implement corrective actions to address risks to timelines, enrollment, or study quality. Ensure accurate and timely reporting of adverse events (AEs) and serious adverse events (SAEs). Maintain complete and compliant drug and device accountability records. Oversee IRB submissions, amendments, continuing reviews, and regulatory documentation. Manage vendor compliance and regulatory readiness for audits and inspections. Business Growth Develop physician outreach and community engagement. Increase patient enrollment. Strengthen sponsor and CRO relationships. Support new study opportunities. Improve operational efficiency. Support future site expansion. Financial Performance Drive Business Performance Own the operational and financial performance of the site by monitoring: Budgets Enrollment KPIs Revenue Study profitability Who You Are You're a leader who thrives on building teams, solving complex challenges, and delivering measurable results.

You enjoy:

Coaching and developing high-performing teams. Building trusted relationships with sponsors, physicians, and CRO partners. Improving operational performance. Taking ownership and driving results. Creating exceptional experiences for patients and study participants. Qualifications Required 5+ years of clinical research experience. Demonstrated experience leading clinical research operations or managing a research site. Bachelor's degree or equivalent experience. Strong knowledge of FDA regulations, ICH-GCP, and clinical research operations. Preferred 7+ years of clinical research experience. Experience managing multiple clinical trials simultaneously. Nursing, allied health, or other clinical background. CCRP, CCRC, or equivalent certification. Experience managing study budgets and sponsor relationships. Your First Year Within your first 12 months you will: Build an engaged, high-performing team. Increase patient enrollment and retention. Strengthen sponsor and CRO relationships. Maintain inspection-ready compliance. Position the site for continued growth and future study awards. Benefits Competitive salary Performance bonus Medical, Dental & Vision 401(k) with company match Generous Paid Time Off Professional Development Career Growth Physical Requirements Ability to lift, carry, push, or pull up to 10 pounds. Ability to sit, stand, walk, bend, and move throughout the workday. Adequate coordination and dexterity to handle equipment and assist patients safely. Why This Role Matters Every study we conduct has the potential to improve lives. As Site Manager, your leadership will directly impact patient care, research quality, and the future growth of clinical research within your community. If you're looking for more than your next job—if you're looking for an opportunity to lead, grow, and make a lasting impact—we encourage you to apply.

Work Location:

In person