Clinical Research Job at Parexel | Apply Now
Clinical research job opportunities continue to grow globally, and Parexel is currently hiring an experienced Clinical Research Associate (CRA) in Shenyang, Liaoning, China. This role offers professionals the opportunity to contribute to clinical trials, support study sites, ensure regulatory compliance, and work with one of the leading organizations in the clinical research industry. If you are looking for a job in China, this opportunity could be the next step in your clinical research career.
- Job Position: Clinical Research Associate (CRA)
- Company Name: Parexel
- Location: Shenyang, Liaoning, China
- Job ID: R0000041493
- Category: Clinical Trials
About the Company
Clinical research role seekers looking for global opportunities often consider Parexel careers because of the company’s strong presence in the pharmaceutical, biotechnology, and medical device sectors. Parexel is a leading clinical research organization (CRO) that supports the development of innovative therapies through comprehensive clinical trial management, regulatory consulting, and market access solutions. The company works with healthcare organizations worldwide to accelerate drug development while maintaining high standards of quality and compliance.
Clinical Research Job Description
Clinical research role professionals joining Parexel as a Clinical Research Associate will support study performance at clinical sites, conduct monitoring visits, ensure compliance with study protocols, and maintain high-quality clinical trial data. The role requires collaboration with investigators, study teams, and regulatory stakeholders to ensure successful trial execution.
Qualifications
Clinical research job applicants should meet the following qualifications:
Education
Bachelor’s degree in Biological Science or a healthcare-related field, or equivalent qualification.
Experience
- Minimum 2 years of experience as a Clinical Research Associate (CRA).
- Experience performing all tasks associated with a CRA position.
- Ability to read, write, and speak fluent English.
- Fluency in the host country language is required.
Clinical Research Job – Key Responsibilities
Clinical research Role responsibilities for this role include:
- Monitor study sites and conduct onsite visits in compliance with study protocols and regulatory requirements.
- Support site selection, investigator training, and study performance improvement.
- Maintain essential study documentation and manage study supplies and drug accountability.
- Perform source data verification (SDV) and ensure timely resolution of data queries.
- Report Serious Adverse Events (SAEs) accurately and on time.
- Track patient recruitment, site progress, and update study systems within required timelines.
- Assist with audits, inspections, and compliance activities.
- Adhere to company policies, ICH-GCP guidelines, and applicable regulations.
- Complete required training, timesheets, expense reports, and CV updates.
Required Skills
Clinical research job candidates should possess the following skills:
- Understanding of clinical data flow and clinical trial processes.
- Knowledge of drug development, GCP/ICH guidelines, and local regulations.
- Strong Microsoft Office and computer proficiency.
- Fluent written and spoken English communication skills.
- Excellent collaboration, interpersonal, and problem-solving abilities.
Conclusion
If you are seeking a rewarding clinical research job, this job offers the chance to work on innovative clinical trials while contributing to the development of new healthcare solutions. With strong career growth prospects, exposure to global research projects, and a collaborative work environment, this role is ideal for experienced CRA professionals looking to advance their careers. Explore Parexel careers today and take the next step toward building a successful future in clinical research and drug development.
