Parexel is seeking a scientifically driven professional to support global clinical research programs by reviewing, interpreting, and negotiating genetic and biomarker informed consent language. You'll play a critical role in ensuring biospecimens and patient data are used in accordance with participant consent while partnering with leading pharmaceutical and biotech organizations. This is a full-time, fully remote position and embedded within the partnership. Client team works EST hours. You will be working across all therapy areas.
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Job Type
Full-time
Career Level
Mid Level