Remote Clinical Scientist: Trial Ops & Data Quality

Parexel

Lincoln (NE)

Remote

USD 85,000 - 110,000

Full time

10 days ago

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Job summary

Parexel is seeking a Clinical Scientist to support the clinical/scientific conduct of complex studies in line with ICH-GCP. The role includes medical monitoring, data reconciliation, and preparation of materials for governance and stakeholder meetings.

The ideal candidate has 2+ years of pharma or clinical development experience, oncology posting familiarity, and strong communication skills. Remote-friendly with potential on-site requirements in the US.

Qualifications

2+ years in pharmaceutical or clinical drug development in the last 5 years.
TA-specific oncology IDV and GSM experience preferred.
Indication-specific experience preferred.
Experience reviewing and resolving study data issues and data queries with sites.

Responsibilities

Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, protocol deviation management).
May support a single study or multiple studies.
May lead a study with limited scope (e.g., Survival Follow-up).
Interact with internal and external stakeholders (study sites, committees) to support study objectives.