Abbott Project Manager, Vascular Clinical Research in Sylmar, California

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

Job Description

We are recruiting an experienced Clinical Research Project Manager to support our Cardiac Arrhythmias and Heart Failure division.

The selected candidate will be responsible for global project management of Heart Failure 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.

Job Responsibilities:

  • 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.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email