CareerPlan

(Senior) Clinical Research Associate

Germany, FrankfurtFull-time2026-09-24 → 2026-11-11
No visa sponsorship

Core

Conduct clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety.

Role type

Clinical Research Associate (CRA II)

Builds

Clinical trial data and documentation for pharmaceutical sponsors

Domain

Clinical research / Pharmaceutical trials

Deliverable

client delivery

Required skills

Clinical trial monitoring, site management, protocol compliance, data integrity, ICH-GCP guidelines, data review, query resolution

Preferred skills

None stated

Technologies

None stated

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits; Ensure protocol compliance, data integrity, and patient safety; Collaborate with investigators and site staff; Perform data review and resolution of queries; Prepare and review study documentation

Seniority

Mid-level, hands-on IC