Associate Clinical Research Study/Project Manager

Employment Type: Full-time Location: Remote - US (Lower 48 States) Estimated Pay Range: $72,000.00 - $90,000.00

Position Overview

iRhythm is seeking a highly motivated and organized Associate Clinical Research Study/Project Manager to support the planning, execution, and oversight of one or more clinical research projects. This role will work closely with Senior Clinical Research Study Managers and other members of the clinical research team to ensure the successful completion of clinical trials.

Responsibilities

• Assist in the planning, execution, and oversight of clinical research projects.
• Coordinate activities of cross-functional teams.
• Ensure compliance with protocols and standard operating procedures.
• Monitor progress against project timelines and budgets.
• Work closely with study coordinators, investigators, and sponsor representatives to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Assist in the development and review of study-related documents (protocols, informed consent forms, case report forms, study manuals).
• Participate in study start-up activities (site identification, feasibility assessment, study initiation visits).
• Assist with the management of study vendors (CROs, external service providers).
• Coordinate the activities of study monitors and provide guidance and support.
• Track and report on study progress (enrollment, data collection, data management).
• Participate in the preparation of study reports, presentations, and publications.

Requirements

• Bachelor's degree in a health-related field or relevant work experience in clinical research.
• 3+ years of experience in clinical research project management or a related field.
• Knowledge of regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Excellent organizational, communication, and problem-solving skills.
• Ability to prioritize and multitask effectively.
• Strong attention to detail and accuracy.
• Proficiency with Microsoft Office Suite.
• Experience with electronic data capture systems.

Work Environment / Other Requirements

• Ability to work independently and as part of a team in a fast-paced, deadline-driven environment.
• Willingness to learn and take on new challenges.

Company Information

Career-defining. Life-changing. At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career.

What’s In It for You:

• Remote position, based anywhere in the lower 48 states.
• Opportunity to work with an amazing group of people who love what they do and believe finding answers for patients and study participants is the most important part of their work.

iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with applicable law. As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives.