job title: Clinical operation specialist(syneos)

Roles and 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