Per Med Clinical ResearchClinical Research Manager
Aug. 2015 - Sep. 2016• Assisted with the preparation of IRB applications, including protocol and informed consents and obtains approval to conduct the study. • Maintained various contracts – i.e., physician contracts, lease agreements, etc. Also responsible for storage of original documents, tracking expiration dates and scanning into an electronic file system.
• Maintained appropriate correspondence with the IRB, including adverse events, annual renewals and protocol amendments. • Ensured compliance with established hospital policies, procedures, objectives, quality controls and regulatory standards and requirements.
• Obtained informed consent and HIPAA authorization, conduct intake interview, and enroll subjects. • Maintaining and coordinating meeting schedule and travel arrangements for CEO.
• Coordinated activities by scheduling work assignments, setting priorities, and directing the work of subordinate employees. Participated actively in the planning and distribution of patient assignments
• Created and maintains database of subject information and generates reports and shipments of data to coordinating center, as needed. • Was responsible for screening, responding and prioritizing incoming communications (phone, voicemail, email, etc.) with CEO. • Provided clerical support for the CEO and COO, as needed. To include: typing memos/letters, distributing the memos/letters, copying, faxing, pulling files, filing, etc.