Job summary
Job post source
This job is directly from Alcanza Clinical Research
Job overview
The Clinical Research Coordinator at Alcanza Clinical Research ensures the execution of clinical studies in compliance with regulatory standards, impacting the company's multi-phase research operations.
Responsibilities and impact
The CRC conducts patient screening, consents, follow-ups, data entry, vital sign collection, lab procedures, scheduling, documentation, adverse event reporting, and supports study start-up and monitoring under supervision.
Compensation and benefits
Full-time employees working 30+ hours weekly are eligible for benefits including medical, dental, vision, life insurance, disability insurance, health savings accounts, supplemental insurances, and a 401k plan with safe harbor match starting the month after hire.
Experience and skills
Requires a Medical Assistant diploma, LPN/LVN, EMT credential, or Associate’s degree with 1+ year clinical research or clinical experience; proficiency in basic clinical procedures and computer applications; BLS certification preferred; bilingual English/Spanish a plus.
Company information
Alcanza Clinical Research is a growing multi-site, multi-phase clinical research company with locations across multiple states and expertise in various therapeutic areas including vaccines and neurology.
Job location and travel
The position is located at Accel Research Sites in DeLand, Florida.
Company overview
Alcanza Clinical Research is a leading organization specializing in conducting clinical trials to advance medical science and improve patient care. They generate revenue by partnering with pharmaceutical companies, biotechnology firms, and medical device manufacturers to facilitate and manage clinical studies. Founded with a mission to accelerate the development of new treatments, Alcanza has a history of delivering high-quality, reliable data that supports regulatory submissions and market approvals. Their expertise spans various therapeutic areas, making them a pivotal player in the clinical research industry.
How to land this job
Position your resume to emphasize your experience with clinical procedures such as blood pressure measurement, vitals, EKGs, and phlebotomy, aligning with the Clinical Research Coordinator role at Alcanza Clinical Research.
Highlight your knowledge of GCP, ICH, FDA regulations, and HIPAA compliance, as well as your ability to manage patient consents, data entry in EDC systems, and study documentation effectively.
Apply through multiple channels including Alcanza Clinical Research's corporate careers page, LinkedIn, and other job boards to maximize your chances of being noticed.
Connect with current Clinical Research Coordinators or Operations team members at Alcanza on LinkedIn; start conversations by asking about their experiences with multi-phase studies or how they manage compliance across multiple sites.
Optimize your resume for ATS by incorporating keywords from the job description like 'clinical research coordinator,' 'GCP,' 'EDC,' 'patient consents,' 'phlebotomy,' and 'HIPAA compliance' to ensure it passes automated screenings.
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