Remote Clinical Data Associate II: Global Trials

Parexel; United States; Remote; USD 60.000 - 90.000; Vollzeit

Benefits dieser Stelle

Medical Aid Contribution

Gap Cover

Life Assurance

Provident Fund (8%)

13th Cheque

Zusammenfassung

Parexel is seeking a Clinical Data Associate II to support global clinical research programs. The role focuses on delivering high-quality data management activities across Phase I–IV studies, ensuring data integrity, regulatory compliance, and cross-functional collaboration.

You will partner with clinical teams, statisticians, programmers, and vendors to ensure accurate data collection, review, and database management. This is a remote-capable position supporting a sponsor-driven program.

Qualifikationen

• Bachelor’s degree in a scientific or healthcare-related field.
• At least two years of data management experience in pharma/biotech.
• Understanding of Phase I–IV studies and data management activities.
• Knowledge of ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR Part 11, MedDRA, WHO Drug Dictionaries.
• Experience with EDC systems; RAVE preferred.
• Strong communication, organizational and problem-solving skills.

Aufgaben

• Lead a small clinical study or co-lead larger studies with moderate guidance.
• Support multiple clinical studies ensuring data quality and timely delivery.
• Manage data management activities performed by CROs and vendors.
• Review study protocols and evaluate eCRF design.
• Collaborate with CRAs, programmers, study managers, and statisticians on annotated eCRFs.

Kenntnisse

Attention to detail

Analytical thinking

Organizational skills

Cross-functional collaboration

Regulatory compliance mindset

Experience with EDC systems

Ausbildung

Bachelor’s Degree in science/healthcare

Tools

RAVE

Electronic Data Capture (EDC) systems

CDISC standards

Jobbeschreibung

Parexel is seeking a Clinical Data Associate II to support global clinical research programs. The role focuses on delivering high-quality data management activities across Phase I–IV studies, ensuring data integrity, regulatory compliance, and cross-functional collaboration.

You will partner with clinical teams, statisticians, programmers, and vendors to ensure accurate data collection, review, and database management. This is a remote-capable position supporting a sponsor-driven program.