Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Lead Clinical Research Coordinator
Job
Futuro Clinical Trials
McAllen, TX (In Person)
$60,000 Salary, Full-Time
Review key factors to help you decide if the role fits your goals.
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
83
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Lead Clinical Research Coordinator Futuro Clinical Trials McAllen, TX Job Details Full-time From $60,000 a year 2 hours ago Benefits Health insurance 401(k) Paid time off Career development plan Professional development assistance Qualifications Nursing Bachelor's degree in psychology Data integrity and documentation Bachelor's degree Psychology Clinical quality assurance standards Healthcare research Full Job Description About Us Futuro Clinical Trials is a multi-therapeutic research site dedicated to delivering high-quality clinical studies with integrity and care. Our team is committed to advancing science while preserving the reputation we've built on reliability and excellence. Position Overview We are seeking a Lead Clinical Research Coordinator with 5 or more years of experience to join our team. This role is designed for someone who has built a foundation in clinical research and is ready to take on more responsibility, while still benefiting from support and mentorship from senior CRCs and Principal Investigators. Responsibilities Lead and coordinate clinical trial activities with growing independence. Ensure adherence to Good Clinical Practice (GCP), site SOPs, and applicable regulations. Assist in subject recruitment, informed consent, and study visit coordination. Maintain accurate regulatory documentation and source records. Communicate effectively with study monitors, sponsors, and the research team. Collaborate with senior CRCs and Principal Investigators for complex regulatory or study-related tasks. Requirements 5 or more years of clinical research experience (required). Bachelor's degree(life sciences, nursing, psychology, or related field) or equivalent site-based experience. Solid understanding of clinical trial conduct and GCP guidelines. Strong organizational and communication skills. Ability to work independently while collaborating with a team. Able to work weekends when required per trials Compensation & Benefits Competitive pay, commensurate with experience. Paid Time Off (PTO). 401(k) retirement plan. Ongoing professional development opportunities.