BS Life Science Jobs at Caidya | Apply Now For The Clinical Research Associate Role
Caidya is hiring a Clinical Research Associate II in Shanghai, China. This role offers an opportunity to work with a leading global CRO, ensuring clinical trial quality, compliance with GCP/ICH guidelines, and subject safety. If you have a life science background and experience in clinical research monitoring, this position is an excellent step in advancing your career.
- Job Position: Clinical Research Associate II
- Location: Shanghai, China
- Job ID:ย 8078
About the Company โ Caidya
Caidya is a leading mid-sized global Clinical Research Organization (CRO) established in 2021 through the merger of dMed and Clinipace. Operating across more than 23 countries, the company provides full-service clinical trial solutions, including pre-IND strategy, clinical operations, regulatory submissions, and post-approval support. With strong expertise in oncology, hematology, rare, and pediatric diseases, Caidya combines scientific excellence with data-driven decision-making to deliver high-quality, efficient, and transparent clinical trials. The organization emphasizes collaboration, adaptability, and the use of proprietary technologies to enhance trial agility and client partnerships. Recognized with the 2023 CRO Leadership Award for overall capabilities, Caidya continues to expand globally, supported by a $165 million strategic investment from Rubicon Founders to drive innovation and growth in the CRO industry.
Job Description
As a Clinical Research Associate II at Caidya, you will:
- Monitor investigational sites to ensure compliance with protocols, GCP, and regulatory guidelines.
- Act as the primary liaison between sponsors and research sites.
- Conduct pre-study, initiation, interim monitoring, and close-out visits.
- Verify informed consent, eligibility, and data accuracy.
- Ensure proper recording, reporting, and resolution of adverse events.
- Manage site documentation, regulatory binders, and investigational product accountability.
- Participate in project team meetings, audits, and the execution of the monitoring plan.
- Identify, escalate, and resolve site issues effectively and independently.
Key Responsibilities
- Maintain working knowledge of assigned protocols and monitoring plans.
- Support project and clinical operations teams with study execution.
- Reconcile regulatory documents and ensure data integrity.
- Provide quality trip reports, follow-up letters, and timely documentation.
- Manage the storage, inventory, and accountability of investigational products.
- Participate in feasibility assessments, investigator meetings, and site audits.
- Adhere to company quality management systems and regulatory standards.
Qualifications
- Bachelorโs degree in life sciences, healthcare, or a related field.
- Clinical research monitoring experience (CRO or pharmaceutical industry preferred).
- Strong knowledge of GCP/ICH guidelines and medical terminology.
- Excellent communication, organizational, and problem-solving skills.
- Proficiency in Microsoft Office and clinical data systems.
- Ability to work independently and travel up to 80%.
- Proficient in both English and the local language.
Keywords: Clinical Research Associate, Clinical Research Job, Shanghai, China, BS Life Science Jobs at Caidya, Pharmaceutical Industry, Job Postings.
