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Clinical Trial Manager - Remote Job

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Date: Apr 1, 2021

Location: Arden Hills, MN, US, 55112

Company: Boston Scientific

Additional Locations: (n/a)



Purpose and Passion • Comprehensive Benefits • Life-Work Integration • Community • Career Growth

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.


**This role has the opportunity to be remote


About the role:

The Rhythm Management Clinical Trial Manager is responsible for the design, planning, execution and leadership of clinical studies and clinical programs worldwide.  They are also responsible for leading cross functional clinical teams in support of the organization's business objectives for product development and/or commercialization.  Possesses a technical knowledge of products, processes, and regulatory requirements for clinical trials conducted within a given therapeutic area.


Your responsibilities will include:

  • Writes study protocols, protocol amendments, informed consents, clinical study project timelines and scientific papers for publication by evaluating scientific literature and publications, analyzing scientific data and staying abreast of current clinical practice.  Efforts and leadership supports product approval, indication expansion and claim support, and mandated post market requirements.
  • Leads the development of clinical strategy and trial design by conducting meetings with the appropriate departments and individuals to obtain feedback/direction. Provides project leadership and scientific expertise throughout the development and implementation of local or global clinical studies.
  • Provides clinical input for new product development, post market surveillance, recertification and business development.
  • Interacts with various study support groups in order to assist in clinical strategy, the development of study plans, and project deliverables. Interacts with regulatory agencies as needed, and will use their scientific knowledge in order to provide directives to staff as well as study sites.
  • Facilitates communication between Sales and Marketing, R&D, Regulatory Affairs, Training, Senior Management, Key Opinion Leaders/investigators and investigational sites by conducting team meetings, drafting and sending routine correspondence (e.g., newsletters) and by presenting regular updates to senior staff (BPT/PIB, etc).
  • Manages clinical study timelines, budget by utilizing the appropriate project management tools, selecting providers, managing vendor contracts and ensuring expenditures are within budgetary guidelines in partner with the Clinical Project Management Office.
  • Facilitates regulatory submissions and communications by communicating with Regulatory Affairs during the submission process.
  • Presents scientific data by communicating accurate, succinct summaries of clinical study work at industry gatherings, investigational meetings and regulatory agency meetings.
  • Provides accurate progress reports on clinical projects by writing assigned clinical portions of reports for submission to regulatory agencies, Institutional Review Boards, Medical Ethics Committees, etc.  May include clinical risk management activities including input into Hazard Analyses, product FMEA and DFUs and authorship of Clinical Evaluation documents (CES, CRBA, CDSR) for identification of harms and support of safety performance for product approval.
  • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.


What we’re looking for in you:

Minimum qualifications

  • Bachelor’s degree and 8+ years of related work experience or an equivalent combination of education and work experience
  • Clinical trial experience required
  • Knowledge of US and EU regulations governing the conduct of clinical studies

Preferred qualifications

  • Strongly prefer a professional with a wide-range of experience and expertise in cardiovascular field, diagnostics for heart failure and/or other cardiovascular disease states
  • Ability to apply comprehensive technical knowledge of a particular field to resolve complex issues in creative ways
  • Ability to use in-depth knowledge of business unit functions and cross group dependencies/relationships


About us

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


Requisition ID: 477202


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