CareerPlan

Informed Consent Specialist II

Spain, MadridFull-time2026-10-27 → 2026-11-11

Core

Lead the development, review, and oversight of informed consent documents (ICFs) for complex, global clinical trials.

Role type

Senior Informed Consent Specialist

Builds

Global and local informed consent forms aligned with protocol and regulatory requirements

Domain

Clinical research / Healthcare / Regulatory affairs

Required skills

Informed consent strategy, GCP knowledge, regulatory compliance, translation oversight, stakeholder management, training and mentorship

Preferred skills

None stated

Technologies

None stated

Responsibilities

Lead creation and optimization of global/local ICFs; Advise study teams on consent strategy and country-specific considerations; Oversee translation and version control; Interface with sponsors and ethics committees; Develop guidance and templates; Provide training to junior team members

Seniority

Senior, hands-on IC