Qualifications
*Bachelor’s degree in a health science, nursing, biology, public health, or related field preferred.
*Minimum of 1–3 years of experience in clinical research coordination or healthcare environment preferred.
*Knowledge of ICH-GCP guidelines, FDA regulations, and human subject protection standards.
*Experience coordinating clinical trials and interacting with sponsors, CROs, investigators, and study participants.
*Strong understanding of clinical research processes, informed consent procedures, and regulatory documentation.
*Ability to manage multiple studies and priorities in a fast-paced environment.
Proficiency with electronic medical records (EMR), EDC systems, and Microsoft Office applications.
*Excellent communication, organizational, and problem-solving skills.
*Ability to work independently and collaboratively within a multidisciplinary team.
Skills
*Clinical trial coordination and study management
*Regulatory and GCP compliance
*Patient recruitment and scheduling
*Informed consent process management
*Source documentation and data entry
*Sponsor and CRO communication
*Query resolution and EDC management
*Time management and multitasking
*Attention to detail and documentation accuracy
*Team collaboration and interpersonal skills
*Problem-solving and critical thinking
*Research participant engagement and retention
*Administrative and operational support
*Knowledge of clinical research ethics and protocols
Clinical Research Coordinator (CRC) works with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study. The clinical research coordinator reports primarily to the Principal Investigator with associated responsibilities to the department head, division administrator or program administrator.
Life Clinical Trials is a multidisciplinary clinical research site, located in Florida/USA, that delivers high quality clinical research services through a highly trained, experienced and dedicated staff. We provide ethical and safe medical care for our volunteers and high quality, clean data to our sponsors with strict adherence to good clinical practice guidelines. Our investigators are board certified in their therapeutic specialties, with colleagues and patients frequently relying upon their medical expertise. Our strong relationship with our patients and associated medical practices aids in successful recruitment, compliance and retention in our clinical research studies.
Life Clinical Trials has worked with most major pharmaceutical companies and CRO’s and is committed to providing high-quality study results with reliable clinical data, in addition to providing high quality care to patients. Our associates have been conducting clinical research since 1995 in Latinamerica and USA, earning a reputation for excellence, quality and consistency.