Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries.
We are recruiting an experienced Clinical Research Project Manager to support our Neuromodulation division.
The selected candidate will be responsible for global project management of Neuromodulation clinical trials. As a Clinical Project Manager, you will provide project management expertise throughout the development and implementation of clinical studies. You will interact with various study support groups and the business unit in order to assist in clinical strategy, the development of study plans and project deliverables.
Facilitating site selection process by conducting meetings with appropriate departments and individuals to review and revise draft site list as necessary. Managing clinical study timelines, budget by utilizing the appropriate project management tools, selecting providers, managing vendor contracts and ensuring expenditures are within budgetary guidelines. Facilitating regulatory submissions and communications. Facilitating the development of clinical execution strategy by conducting meetings with the appropriate departments and individuals to obtain feedback/direction. Overseeing compliance to study requirements.
The required skills and experiences are:
Completed Bachelor’s degree. Degree preferred in biological sciences or related medical/scientific field.
Proven experience in project management with 1 to 3 years of experience. Minimum 3 years’ experience in clinical trial management. Fluency in English (any other language is an asset). Flexibility combined with excellent interpersonal skills. Ability to influence others to achieve positive results and collaboration. Good knowledge of FDA regulations for clinical trials and OUS knowledge is helpful. Knowledge of clinical trials in medical device or other industry preferred and outcomes research study design. Demonstrated ability to work effectively on cross-functional teams.