Biomarkers and Genomic Medicine Informed Consent Specialist

Parexel is looking for a Biomarkers and Genomic Medicine Informed Consent Specialist! This is a remote position!

Responsibilities include:Review of approved trial informed consent documents to determine allowable retention and utilization of biospecimens and dataAbility to identify complex biospecimen related consent permissions and accurately categorize into common fields  Engaging and communicating within the team for knowledge sharingEscalating any ambiguous or unclear informed consent language identified for discussion and decision making by the team

Education:Requires a bachelor’s degree with a concentration in a scientific- or technical-related discipline

Knowledge and Experience:At least 2 years in the biopharma industry (clinical trial operations, clinical specimen management, biobanking/biorepositories, biomarker and/or genetics research, etc.)Direct involvement working with informed consent documents requiredKnowledge of global biospecimen processes specific to biomarker discovery and development preferred

Skills:Client-focused approach to workExpertise in MS Office applications including Excel and PowerPointExcellent written and oral communication skills in EnglishOrganization, attention to detail and effective time management skillsStrong analytical and critical thinking skillsAbility to manage in a fast-paced, team-based environment and work independently when needed

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