Associate Clinical Research Project Manager

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

About This Role:

• Assist the Clinical Research Study/Project Manager in the planning, execution, and oversight of clinical research projects, including coordinating the activities of cross-functional teams, ensuring compliance with protocols and standard operating procedures, and monitoring progress against project timelines and budgets.
• Work closely with study coordinators, investigators, and sponsor representatives to ensure that study activities are conducted in compliance with applicable regulatory requirements and guidelines, including Good Clinical Practice (GCP) guidelines.
• Assist in the development and review of study-related documents, such as protocols, informed consent forms, case report forms, and study manuals.
• Participate in study start-up activities, including site identification, feasibility assessment, and study initiation visits.
• Assist with the management of study vendors, including clinical research organizations (CROs) and other external service providers, to ensure that services are provided in a timely and cost-effective manner.
• Coordinate the activities of study monitors and provide guidance and support as needed.
• Track and report on study progress, including enrollment, data collection, and data management.
• Participate in the preparation of study reports, presentations, and publications.

Experience and Minimum Qualifications:

• 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 related field.

Knowledge, Skills and Abilities:

• Knowledge of regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Excellent organizational, communication, and problem-solving skills, with the ability to prioritize and multitask effectively.
• Strong attention to detail and accuracy.
• Proficiency with Microsoft Office Suite and 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.

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.

Location:

Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

Estimated Pay Range

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

iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops@irhythmtech.com

About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm's vision is to deliver better data, better insights, and better health for all.

Make iRhythm your path forward. Zio, the heart monitor that changed the game.

There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a @irhythmtech.com email address. Please check any communications to be sure they come directly from @irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact taops@irhythmtech.com. Written offers of employment will be extended in a formal offer letter from an @irhythmtech.com email address ONLY.

For more information, see https://www.ftc.gov/business-guidance/blog/2023/01/taking-ploy-out-employment-scams and https://www.ic3.gov/Media/Y2020/PSA200121