Research Assistant

• Conducts and manages minimal risk studies under the supervision of a project manager or designee. • Prepares, maintains, and tracks regulatory documents according to governmental regulations and sponsor requirements. • Assists with subject visits including obtaining vital signs, performing clinical tests, collecting clinical samples, and data collection, as applicable. • Sets-up, tracks, and trouble-shoots study technology (i.e., e-diaries, apps, home use research equipment), as applicable. • Conducts literature searches and fact-finding research to support project development • Ensures adherence to federal or other regulatory requirements. • Communicates needs, issues, statuses, etc. to appropriate study personnel. • Assists with grant submissions and grant funding opportunities; participates in pre- and post-award grant process, as applicable. Work is typically performed in an office environment. Accountable for satisfying all job specific obligations and complying with all organization policies and procedures. The specific statements in this profile are not intended to be all-inclusive. They represent typical elements considered necessary to successfully perform the job.