Senior Clinical Data Associate - Remote, Quality Lead

Parexel; United States; Remote; USD 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Medical Aid Contribution

Gap Cover

Life Assurance

Provident Fund (8%)

13th Cheque

Zusammenfassung

Parexel is seeking a Senior Clinical Data Associate to join our team remotely. You will support global clinical programs from Phase I–IV, ensuring data quality, regulatory compliance, and timely study execution.

You will partner with clinicians, statisticians, programmers, CRAs, vendors, and study managers to manage data capture, review, and database activities. You will lead data management tasks, coordinate EDC systems, develop study documentation, and contribute to database lock and study

Qualifikationen

• Strong attention to detail and analytical thinking.
• Experience in clinical research and regulated environments.
• Ability to collaborate across multidisciplinary teams and external partners.
• Patient-focused mindset with commitment to data quality and regulatory compliance.
• Comfort with EDC systems and multiple platforms.

Aufgaben

• Lead a small clinical data management study or co-lead larger studies with moderate guidance.
• Support multiple studies ensuring high data quality and timely delivery.
• Manage data management activities by CROs and vendors.
• Review study protocols and eCRF design, develop annotated CRFs and guidelines.
• Develop data edit checks and study data listings as needed.
• Coordinate design, testing, and issue resolution of EDC systems.
• Maintain study Data Management Plans and supporting docs.
• Perform query management, external data reconciliations, and SAE reconciliation.

Kenntnisse

Attention to detail

Analytical thinking

Organizational skills

Communication skills

Regulatory compliance

Ausbildung

Bachelor's Degree in a scientific or healthcare-related field

Tools

RAVE

Jobbeschreibung

Parexel is seeking a Senior Clinical Data Associate to join our team remotely. You will support global clinical programs from Phase I–IV, ensuring data quality, regulatory compliance, and timely study execution.

You will partner with clinicians, statisticians, programmers, CRAs, vendors, and study managers to manage data capture, review, and database activities. You will lead data management tasks, coordinate EDC systems, develop study documentation, and contribute to database lock and study