# Clin Ops Specialist

**Company**: Syneos Health
**Location**: Shanghai
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/COS_25101452?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c009490b-be1

## 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

## Skills

### Required
- clinical research protocols
- regulatory requirements
- communication skills
- organizational skills
- time management
- Microsoft Office Suite
- clinical trial management software

### Nice to have
- Associate's degree or higher in a related field
- Certified Clinical Research Coordinator (CCRC) or equivalent certification

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/COS_25101452?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)