Organization:Pediatric GeneticsJob Summary:JOB SUMMARYPerforms a variety of duties involved in the collection, interpretation, and documentation of data in support of clinical trials with occasional guidance. Assists in ensuring adherence to protocols, appropriate regulations, and deadlines..KEY RESPONSIBILITIES* Coordinate protocol and patient consent form process and develop assessment tool per protocol to use in clinical research.* Coordinates preparation of all IRB and regulatory documents; under direction of PI may draft various communications with Sponsor.* Identifies