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At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose-improving lives through your life's work.
About the role:
The Post Market Clinical Project Manager is responsible for project planning for Post Market Clinical Follow Up (PMCF) activities globally. They work collaboratively to support development of budgets, schedules and resource plans to support PMCF throughout the project life cycle. They consult with functional and business leads to implement achievable PMCF activities.
Your key responsibilities will include:
In collaboration with PMCF senior management, leads and drives the planning, execution and management of budget and schedule aspects of PMCF activities.
Collaborates with Clinical Risk to develop content and structure for PMCF surveys, focus groups, and retrospective data reviews.
Collaborates with Sales team to identify physicians and sites to participate in surveys, focus groups, and retrospective data reviews.
Communicates and collaborates directly with physicians and sites to plan and execute on PMCF activities.
Manages recurring project meetings; ensures accountability across the team for deliverables.
Tracks development and schedule of all internal and external project materials.
In collaboration with senior management and project team, leads the proactive identification, assessment, and management of PMCF timeline and budget risks
Approximately 20% travel including United States and Europe
What we're looking for in you:
Bachelor's degree and 5+ years of related work experience or an equivalent combination of education and experience.
Clinical trial and/or Project Management experience or equivalent
Strong verbal and written communication skills
Strong ability to collaborate with team members
Excellent problem solving and analytical skills
8+ years of related work experience
Post Market Surveillance and/or Medical Device Vigilance experience
Spreadsheet and database experience
Clinical or Financial planning systems experience
Clinical Trial Research Associate experience
Medical Device Regulation experience
Quality Assurance experience
As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you're looking to truly make a difference to people both around the world and around the corner, there's no better place to make it happen.
Boston Scientific is an Equal Opportunity Employer - Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran
Boston Scientific maintains a drug-free workplace. Pursuant to Va. Code 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.
Requisition ID: 464540