Medix™ · 1 week ago
Bilingual Clinical Research Coordinator - 247871
Leesburg, FL
Full-time
Onsite
Entry, Mid Level
$65K/yr - $74K/yr
2+ years expMedix™ is a company that specializes in clinical research, and they are seeking a Bilingual Clinical Research Coordinator to manage activities throughout the start-up, conduct, and close-out phases of research studies. The role involves ensuring compliance with regulations, accurate data collection, and effective communication with patients and research staff.
CrowdsourcingRecruitingSocial NetworkStaffing AgencyVenture Capital
Hiring Manager
Ashley Kaufman
Responsibilities
Thoroughly understand assigned protocols and ensure all patient visits and procedures are completed as specified
Accurately document patient assessments, observations, test results, and other study-related data following federal regulations and protocol requirements
Obtain informed consent from patients in compliance with federal regulations, GCP, and IRB requirements
Strategically recruit eligible study subjects to meet enrollment targets within sponsor timelines while upholding ethical and regulatory standards
Complete required training promptly
Schedule and conduct patient visits in line with protocol timelines
Maintain complete and precise source documentation for all study activities
Accurately complete and submit case report forms (CRFs/eCRFs) and sponsor worksheets
Safeguard the confidentiality of patient and study information in accordance with HIPAA, confidentiality agreements, and company policies
Promptly report adverse events to the supervisor and/or Principal Investigator/Sub-Investigator as appropriate
Notify the sponsor of Serious Adverse Events (SAEs) within 24 hours of awareness and inform the supervisor and Principal Investigator/Sub-Investigator
Manage and track study materials (e.g., study drug, CRFs, lab supplies) to ensure availability throughout the study
Maintain consistent communication and document interactions with the Team Lead I, Team Manager, Principal Investigator, Sub-Investigators, and other research staff
Participate in required training, conferences, and investigator meetings to remain current with evolving federal regulations and company policies
Continuously seek educational opportunities to deepen knowledge of clinical research processes and regulations
Perform study-related tasks efficiently and cost-effectively, always adhering to company policies
Follow safety procedures in all activities
Represent company Research professionally and courteously in all interactions—verbally, in writing, and in appearance—with patients, staff, sponsors, and external partners
Carry out additional duties as assigned by management
Qualification
Required
Must have 2-5 years of CRC experience
Know a study from start up to close out
Regulatory experience
Phlebotomy/blood draw experience
Must be bilingual in English and Spanish
Bachelor's degree preferred, but not required
Ideally, at least 2 years as a Clinical Research Coordinator (CRC) and 1–3+ years in clinical or biological research
Solid understanding of clinical research methodologies
Strong leadership and team management capabilities
Effective collaboration with operational teams
Excellent verbal and written communication
Proficiency in Office 365 and other relevant software
Experience drafting and reviewing Standard Operating Procedures
Strong problem-solving, risk assessment, and analytical skills
Demonstrated process improvement experience
Effective negotiation and conflict resolution skills
Ability to multitask, prioritize tasks, and remain flexible
Independent thinker able to influence and drive decisions when needed
Benefits
Medical
Dental
Vision
Time off
Paid holidays off
Bonus
401k
Growth opportunities
Company
Medix™
Medix provides workforce solutions to clients and creates opportunity for contract employees.
501-1000 employees
Funding
Current Stage
Late StageTotal Funding
unknown2022-09-16Acquired
Leadership Team
Andrew Limouris
Founder, President and CEO
Brian Anstiss
Chief Financial Officer
Recent News
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