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, UCCT, 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 across numerous indications.
- 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 biospecimen solutions organization, performing prospective and retrospective projects for pharmaceutical partners of all sizes.
- 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 Description
Job Title: Clinical Research Coordinator
Job Summary:
Join a growing clinical research organization dedicated to advancing medicine and improving patient care through high-quality clinical trials.
KUR International is seeking motivated Clinical Research Coordinators to support our expanding network of research sites across multiple locations. We are looking for candidates with clinical research experience who are passionate about delivering high-quality research, maintaining regulatory compliance, and providing an exceptional experience for study participants.
As a Clinical Research Coordinator, you will play a key role in the successful execution of Phase I-IV clinical trials by partnering with investigators, research participants, sponsors, and cross-functional teams to ensure studies are conducted safely, efficiently, and in compliance with regulatory requirements.
At KUR International, we are committed to investing in our employees through ongoing professional development and career advancement opportunities. This position offers the opportunity to grow within our clinical research organization, with placement as a CRC I, CRC II, or CRC III based on your experience, qualifications, and demonstrated competencies, along with opportunities for continued growth as your career progresses.
We are hiring for multiple clinic locations. Final work location and specific responsibilities will be determined based on business needs, candidate experience, and qualifications during the interview process.
Key Responsibilities
Clinical Trial Management:
- Coordinate daily clinical trial activities from study start-up through close-out.
- Recruit, screen, consent, enroll, and schedule study participants.
- Perform protocol-required clinical procedures including vital signs, ECGs, phlebotomy, specimen collection, and sample processing, as applicable.
- Maintain accurate source documentation, case report forms, and investigational product accountability.
- Ensure compliance with FDA regulations, GCP/ICH guidelines, IRB requirements, study protocols, and KUR SOPs.
- Support sponsor monitoring visits, audits, and regulatory inspections.
- Complete required training and maintain certifications.
Communication & Documentation:
- Communicate effectively with investigators, sponsors, CROs, participants, vendors, and internal departments.
- Maintain complete, accurate, and audit-ready study documentation.
- Provide timely updates regarding study progress and participant status.
- Support study close-out activities and regulatory document retention.
- Collaborate with cross-functional teams to ensure successful study execution.
Administrative Duties:
- Maintain equipment logs and calibration records.
- Monitor study supplies and sponsor materials.
- Coordinate vendor shipments and laboratory logistics.
- Respond promptly to study-related communications.
- Maintain a clean, organized, and professional work environment.
- Perform additional duties as assigned.
Technical Skills:
- Experience using Electronic Data Capture (EDC) systems.
- Experience utilizing Clinical Trial Management Systems (CTMS), preferably RealTime CTMS.
- Proficiency with Microsoft Office Suite, Microsoft Teams, DocuSign, and other business applications.
- Ability to accurately document study activities using electronic systems.
- Ability to learn and utilize sponsor-specific technologies and study platforms.
Ideal Candidate Is :
- Organized and detail-oriented.
- Passionate about patient care and clinical research.
- Adaptable in a fast-paced environment.
- Able to manage multiple priorities.
- A strong communicator who enjoys collaborating across teams.
- Committed to maintaining quality, compliance, and participant safety.
Required Qualifications:
- High school diploma or equivalent required.
- Associate's degree or higher in healthcare, life sciences, nursing, or a related field preferred.
- Prior experience in a clinical healthcare or clinical research setting is required.
- Strong communication, organizational, interpersonal, and computer skills.
- Ability to manage multiple priorities while maintaining attention to detail.
Preferred Qualifications:
- Clinical research experience supporting Phase I-IV clinical trials.
- Experience using Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS), preferably RealTime CTMS.
- Working knowledge of FDA regulations, ICH-GCP guidelines, HIPAA requirements, and clinical research documentation.
- Experience performing protocol-required clinical procedures including phlebotomy, ECGs, specimen collection, and processing.
- Experience within therapeutic areas such as wound care, respiratory, vaccines, pediatrics, infectious disease, or other specialty indications is preferred depending on clinic location.
Work Schedule :
- Full-Time
- Monday-Friday
- Flexibility to accommodate participant schedules and study-related activities, which may occasionally require early morning or extended hours.
- Occasional travel between nearby clinic locations may be required.
Physical Requirements:
- Ability to lift, push, or pull up to 10 pounds.
- Ability to sit, stand, walk, bend, stoop, and reach for extended periods.
- Ability to perform protocol-required clinical procedures and specimen handling.
- Ability to work in a fast-paced clinical research environment while maintaining attention to detail.
KUR International is an Equal Opportunity Employer committed to fostering an inclusive workplace where diversity is valued. We provide equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, national origin, age, disability, veteran status, genetic information, sexual orientation, gender identity, or any other status protected by applicable federal, state, or local law.
Work Location: In person
