Precision for Medicine is a leading global clinical research organization (CRO) specializing in biomarker-driven clinical development and translational medicine. The company supports pharmaceutical and biotech firms in accelerating drug development through innovative data management, clinical trial solutions, and precision medicine approaches.
As an Equal Opportunity Employer, Precision for Medicine fosters an inclusive workplace, encouraging diverse talent to apply.
Job Description: Clinical Data Associate II
The Clinical Data Associate II will support clinical trial data management activities from study setup to database lock. This role involves ensuring data accuracy, performing database testing, query resolution, and collaborating with cross-functional teams.
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Key Responsibilities:
- Assist in database development, testing (UAT), and maintenance
- Perform data entry, quality control, and CRF (Case Report Form) review
- Develop edit checks, data validation, and discrepancy management
- Support medical coding (MedDRA/WHODD) and SAE reconciliation
- Generate study metrics and status reports
- Liaise with third-party vendors (EDC, external data providers)
- Ensure compliance with SOPs, regulatory guidelines, and study protocols
- May assist in SAS programming and protocol/SAP review
Qualifications & Skills:
- Education: Bachelor’s degree (Life Sciences, IT, or related field)
- Experience: 2+ years in clinical data management (CDM)
- Technical Skills: Proficiency in Microsoft Office, EDC systems, and basic SAS (preferred)
- Soft Skills: Strong communication, organizational skills, attention to detail
- Industry Knowledge: Familiarity with ICH-GCP, CDISC standards is a plus
Why Join Precision for Medicine?
- Work on cutting-edge clinical trials in precision medicine
- Collaborative, growth-oriented work environment
- Opportunities for career advancement in clinical research
How to ApplyPrecision for Medicine Careers: Data Management Role for Life Science Graduates
