|Title:||Associate Director, Clinical Operations|
|Department:||Research and Development|
You will be responsible for the planning, implementation, execution and management of clinical research studies. In addition, you will manage clinical outsourcing to CROs and other vendors such as IXRS, labs, IRBs, etc. We are looking for candidates with the ability to author, review and approve various study related documents; evaluate issues, interpret data, suggest and implement solutions. Responsible for the financial and budgetary planning and tracking of assigned studies.
Must have a Bachelor’s degree or nursing qualification is required. Scientific/health care field preferred, but not required with at least 5 years of clinical research experience with evidence of increasing responsibility within a pharmaceutical company, CRO or similar organization, experience leading cross functional teams, and detailed knowledge of current regulatory requirements and guidelines governing clinical research.