Syneos FSP COS Clinical Trial Assistant (Contract)
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| Company Name | Syneos Health Consulting (Shanghai) Co., Ltd. |
| Company Type | Private |
| Job Type | Full-Time |
| Salary Range | CN¥10,000.00 |
| Location | Shanghai, Shanghai, China |
| Qualifications | None / No Formal Education |
| Experience | No Experience / Fresh |
Job Overview
Syneos Health is seeking an entry-level Clinical Trial Assistant to join their FSP COS team in Shanghai, China. This contract role offers a foundational opportunity to contribute to clinical research operations, supporting the efficient execution of trials and gaining valuable experience in the pharmaceutical manufacturing sector.
Company Overview
Syneos Health Consulting (Shanghai) Co., Ltd. is part of Syneos Health, a leading fully integrated biopharmaceutical solutions organization. With a global presence, Syneos Health is dedicated to accelerating the development and commercialization of medicines, working across a diverse range of therapeutic areas and providing expertise in clinical research and commercialization strategies.
Quick Details
- Salary Range: CN¥10,000.00
- Job Type: Full-time
- Qualifications: None / Open to all applicants
- Experience: No Experience / Fresh
Key Responsibilities
- Assist with the preparation, distribution, and filing of clinical trial documents.
- Support the clinical team in tracking and managing study-specific documentation.
- Facilitate communication and information flow between study sites and the project team.
- Maintain and update trial master files (TMF) and electronic trial master files (eTMF).
- Schedule and coordinate meetings, ensuring necessary materials are prepared.
- Ensure adherence to standard operating procedures (SOPs) and regulatory requirements.
Requirements
- High school diploma or equivalent; Bachelor’s degree in a life science or related field preferred.
- Strong organizational skills and attention to detail.
- Excellent verbal and written communication skills in English and Mandarin.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work effectively in a team-oriented and fast-paced environment.
- Willingness to learn clinical trial processes and regulations.
Benefits
- Opportunity to gain hands-on experience in clinical trial operations within a global biopharmaceutical company.
- Exposure to industry-leading clinical research methodologies and practices.
- Professional development and potential for career growth in the pharmaceutical sector.
- Work in a collaborative and supportive team environment.
- Competitive monthly compensation.
- Contribution to meaningful work in advancing healthcare solutions.