CRA Job Opportunity at Parexel | Apply Now
CRA job opportunities in the clinical research industry are growing rapidly, especially with leading global organizations like Parexel. The company is currently hiring for the position of Clinical Research Associate II in Shanghai, China. This life sciences job is ideal for candidates with clinical monitoring experience, strong knowledge of ICH/GCP guidelines, and a passion for supporting global clinical trials.
- Job Position: Clinical Research Associate II
- Location: Shanghai
- Job ID:Â R0000041807
About the Company
CRA job opportunities at Parexel offer professionals the chance to work with one of the world’s leading clinical research organizations. PAREXEL specializes in supporting biopharmaceutical companies with clinical development, regulatory consulting, and market access solutions. The company is well known in the life sciences job sector for delivering high-quality clinical trial services across global markets.
CRA Job Description
CRA job responsibilities at Parexel focus on clinical monitoring, investigator site management, patient safety, and regulatory compliance. The Clinical Research Associate II will work closely with investigator sites to ensure studies are conducted according to ICH/GCP guidelines, local laws, and company SOPs.
The selected candidate will conduct source data verification (SDV), ensure timely submission of clinical trial data, and proactively manage site activities to help studies run efficiently. This jobs in China opportunity also involves collaborating with investigators, healthcare professionals, and site personnel to maintain study quality and compliance standards.
Qualifications
Education
CRA job applicants must have:
- Bachelor’s degree or above in Life Sciences or related field
- Equivalent relevant educational background may also be considered
Experience
CRA job experience requirements include:
- At least 1.5 years of Clinical Monitoring or Site Management experience
- 2 years of experience is preferred
- Global study monitoring experience is preferred
- Strong knowledge of ICH/GCP and clinical research regulations
Skills Required
CRA job applicants should possess the following skills:
- Computer literacy including Word, Excel, and PowerPoint
- Proficiency in Chinese
- Good written and spoken English communication skills
- Strong interpersonal and communication abilities
- Ability to manage multiple tasks with attention to detail
- Flexible attitude toward work assignments and learning
- Ability to work effectively in a matrix and teamwork environment
Key Responsibilities – CRA Job
CRA job duties include:
- Monitoring and management of investigator sites, ensuring patient safety, and maintaining high-quality clinical trial documentation.
- Conduct source data verification (SDV) and ensure clinical trial data are submitted to data management in a timely manner
- Identify issues that may impact study conduct and ensure proper issue closure
- Ensure studies comply with ICH/GCP, local laws, and SOPs
- Maintain patient safety and report safety issues according to regulatory requirements
- Inform Principal Investigators (PI) and site staff about study-related issues
- Develop corrective and preventative actions with site personnel
- Maintain effective communication with healthcare professionals and investigator teams
- Enter study data into company systems in a timely manner
- Report study progress after site visits
- Maintain accurate site-level information on clinical trial registries
- Assist in Investigator Initiation Package (IIP) documentation
- Maintain Site Master File (SMF) and Trial Master File (TMF)
- Generate site monitoring reports and maintain monitoring logs
- Complete required training, expense reports, timesheets, and CV updates
- Follow PAREXEL processes and applicable regulatory requirements
Why Consider Parexel Careers?
CRA job opportunities at Parexel provide professionals with exposure to global clinical trials, international regulatory practices, and career growth within the life sciences job industry. The company offers a collaborative environment where employees can contribute to advancing healthcare and clinical research worldwide.
