A global Clinical Research Organization is seeking a Biomarker Consent Specialist to author and negotiate genetic consent language for clinical trials. The ideal candidate has at least 5 years of experience in global clinical trials and genetic informed consents. This role offers flexible work arrangements and the opportunity to contribute to impactful healthcare projects. Key qualifications include strong communication skills, problem-solving abilities, and proficiency in relevant clinical trial systems. Join a collaborative team dedicated to making a difference.
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