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Clinical Research Lead (1+yrs ex rqd)

Job

One of a Kind Clinical Research Center LLC

Scottsdale, AZ (In Person)

$62,502 Salary, Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/20/2026

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Job Description

Clinical Research Lead (1+yrs ex rqd) One of a Kind Clinical Research Center LLC Scottsdale, AZ Job Details Full-time $25 - $31 an hour 1 day ago Qualifications Teamwork Patient monitoring
HIPAA ICH
guidelines Supervising experience Attention to detail Medical laboratory work Managing clinical research teams Healthcare team management Clinical team leadership Clinical quality assurance standards Clinical trial support in drug product development Medical terminology Leading research teams Full Job Description Job Overview We are seeking a dynamic and detail-oriented Clinical Research Lead with at least one year of experience in clinical trials to join our innovative healthcare team. In this pivotal role, you will oversee the planning, execution, and monitoring of clinical studies, ensuring compliance with regulatory standards and company protocols. Your leadership will drive the success of research initiatives that contribute to groundbreaking medical advancements. This position offers an exciting opportunity to influence patient care through meticulous research oversight and collaborative teamwork. This role oversees our Arizona and Texas site alongside another manger. Duties Lead and supervise clinical research projects, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines Coordinate with cross-functional teams including investigators, site staff, and vendors to facilitate smooth trial operations Review and verify study documentation such as informed consent forms, case report forms, and regulatory submissions for accuracy and completeness Monitor patient enrollment, retention, and safety by conducting patient assessments, vital signs measurement, and blood sampling when necessary Oversee clinical laboratory procedures, including blood sampling and analysis, ensuring proper sample handling and documentation Training and onboarding new staff Source building Experience Minimum of one year of supervising experience in clinical trials or related healthcare research settings Proven expertise in clinical trials management from initiation through closeout phases Strong understanding of medical terminology, clinical development processes, and regulatory frameworks such as FDA regulations and ICH GCP guidelines Experience working with EMR systems, clinical laboratory procedures, and blood sampling techniques (phlebotomy) Knowledge of HIPAA regulations to ensure patient confidentiality and compliance during data collection and documentation review Demonstrated ability to monitor patient vital signs, perform blood sampling accurately, and manage clinical trial documentation effectively Certification in Good Clinical Practice (GCP) from a recognized issuer is required; Join us to lead innovative clinical research projects that make a real difference in patient outcomes. We are committed to supporting your professional growth while fostering a collaborative environment dedicated to excellence in healthcare research.
Pay:
$25.00 - $31.00 per hour
Experience:
Pharmaceutical Initiated Clinical trials : 1 year (Preferred) Medical care : 1 year (Preferred)
Work Location:
In person