Preclinical Research Associate II

This position supports Boston Scientific's efforts to develop, test and verify the performance and efficacy of newly designed medical devices using in vitro, benchtop and animal models.

About The Role

The Preclinical Research Associate III is responsible for planning, conducting and reporting preclinical studies, maintaining the integrity of preclinical data, and ensuring project timelines are achieved. This role partners closely with divisional and cross-functional teams to deliver high-quality research that advances innovative medical technologies.

This role follows a hybrid work model requiring employees to be in the local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position. Relocation assistance is not available for this position.

Responsibilities

• Serve as a Study Director/Study Manager for preclinical studies conducted at an internal research facility.
• Design and lead preclinical in vivo, ex vivo and benchtop studies based on device and technology needs, including protocol development, study management, data analysis, interpretation and report generation.
• Collaborate with sponsor teams to establish study timelines that support long-term project goals and objectives.
• Assist in the development of translational models by partnering with internal and external resources.
• Build strong, trusted relationships and contribute to cross-functional collaboration across the preclinical department and other stakeholder functions.
• Demonstrate a passion for learning, innovation and knowledge sharing within the preclinical organization.
• Mentor junior team members, as applicable.

Qualifications

Required qualifications:

• Bachelor's degree in biological sciences, biomedical engineering, biomedical design, biochemistry, veterinary science or a related field.
• Minimum of 2 years' experience in preclinical research or a related field.
• Excellent communication, presentation, analytical and technical writing skills.
• Ability to work independently or semi-independently while contributing effectively in a collaborative, team-based environment.

Preferred Qualifications

• Master's degree in a related field.
• Experience in one or more of the following therapeutic areas: Endoscopy, Urology, Neuromodulation, Cardiology, Cardiac Rhythm Management, Interventional Therapies, Left Atrial Appendage Closure or Electrophysiology.
• Experience serving as a study director for non-Good Laboratory Practice (GLP) and GLP studies. Knowledge of GLP regulations is preferred.
• Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Project and Minitab or other statistical analysis software.
• Demonstrated ability to communicate technical information effectively through presentations, reports and cross-functional collaboration.

Pay

Minimum Salary: $71,500
Maximum Salary: $135,800

The anticipated compensation and benefits will vary based on actual location, experience, education, and other relevant factors. Compensation for this role may also include variable compensation such as annual bonus target and long-term incentives (subject to plan eligibility).