Description
Syneos Health is seeking a Clin Ops Specialist to join their team in Shanghai or Guangzhou. As a Clin Ops Specialist, you will play a crucial role in safeguarding the wellbeing of research subjects, reviewing study protocols, and ensuring compliance with regulatory standards.
Job Responsibilities
- Safeguard the wellbeing of research subjects in a medical capacity, ensuring that all procedures are conducted with the highest standards of care and safety
- Review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards
- Recruit and coordinate communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study
- Follow applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards
- Collaborate with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents
- Monitor trial progress and address any issues that arise during the study
- Provide organizational related support or service, typically under supervision, assisting with administrative tasks and other support activities as needed
- Perform routine tasks with some deviation from standard practice, adapting to changing circumstances and requirements as necessary
- Utilize 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