[Hiring] Clinical Operations Specialist @Syneos Health

Role Description

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.
• Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
• Basic Life Support (BLS) certification required.

Requirements

• 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.

Benefits

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself.
• We are continuously building the company we all want to work for and our customers want to work with.