Senior Clinical Trial Specialist

Senior Clinical Trial Specialist

This role supports the planning, execution, and oversight of clinical trials within Boston Scientific's Renal Denervation (RDN) portfolio. It ensures alignment with project objectives and compliance with regulatory standards while maintaining a continuous state of audit readiness and proactively mitigating study risks. The specialist works closely with cross-functional teams to manage study documentation, systems, and regulatory submissions. A key responsibility involves guiding patients through the screening processfrom informed consent to randomizationand coordinating with both internal stakeholders and external site personnel to ensure smooth and compliant trial operations.

Work Mode: This is a hybrid position in the office minimum three days per week at our Maple Grove, MN or Marlborough, MA location.

Visa Sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position.

Your responsibilities will include:

• Supports the project team in the planning, execution and management of operational aspects of clinical trials.
• With supervision participates in the execution of clinical studies in accordance with the project plans, budget and resource allocations following applicable regulatory and standard operating procedures.
• Tracks development of and collaborates with the project team on all internal and external project materials, processes, manuals, plans, committees, study systems and, as applicable sponsor required regulatory submissions.
• Supports a continuous state of audit readiness, in collaboration with the project team, supports the proactive identification, assessment, and management of clinical study risks.

Required qualifications:

• Bachelor's degree and minimum 4 years of related work experience or an equivalent combination of education and relevant experience
• Proven clinical trial research experience in a medical device industry required
• Proven working experience with clinical trial teams, regulatory teams, global Clinical operations, and clinical research site personnel

Preferred qualifications:

• Preferred experience in cardiovascular medical device trials, preferably with IDE studies
• Ability to effectively collaborate across multiple clinical and non-clinical functions
• Ability to navigate a fast-paced environment and manage multiple projects simultaneously in a tight deadline-driven environment