Job Description

Job Title

Associate Director, Cross Therapeutic Area Clinical Risk Management

Overview

The Associate Director, Cross TA Clinical Risk Management, works with trial teams and/or program teams to coordinate the identification, assessment, and mitigation of quality risks that could impact trial data integrity, patient safety, well‑being, or rights. Throughout the duration of the trial or program, this role executes data‑driven, risk‑based trial oversight activities to deliver quality in the execution of clinical trials (or programs), maintain compliance with regulatory requirements and internal procedures, and sustain inspection readiness.

Key Responsibilities

  • Actively and independently participates in all study activities, contributing to the identification and assessment of key risks in the clinical protocol/set‑up and advising clinical team members on effective mitigation strategies for complex clinical trials, compounds and prog...

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