Job Responsibilities

Safeguarding the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety
Reviewing study protocols and executing procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations
Recruiting and coordinating communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study
Following applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards
Collaborating with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents
Monitoring trial progress and addressing any issues that arise during the study, ensuring that all problems are promptly identified and resolved
Providing organizational related support or service, typically under supervision, assisting with administrative tasks and other support activities as needed
Performing routine tasks with some deviation from standard practice, adapting to changing circumstances and requirements as necessary
Utilizing broad knowledge of operational systems and practices gained through extensive experience and/or education, applying this knowledge to improve study processes and outcomes
Qualifications
High school diploma or equivalent required
Associate's degree or higher in a related field preferred
Minimum of 2 years of experience in clinical operations or a related field
Strong understanding of clinical research protocols and regulatory requirements
Certifications
Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred
Basic Life Support (BLS) certification required
Necessary Skills
Excellent communication and interpersonal skills
Strong organizational and time management abilities
Attention to detail and accuracy in documentation
Ability to work effectively in a team environment
Proficiency in Microsoft Office Suite and clinical trial management software
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