Senior Clinical Project Manager
Abarca HealthFull Time
Senior (5 to 8 years)
Candidates must possess a Bachelor's degree in a health-related field or equivalent work experience in clinical research. A minimum of 3 years of experience in clinical research project management or a related area is required. Proficiency in Microsoft Office Suite and electronic data capture systems is necessary, along with knowledge of regulatory requirements and Good Clinical Practice (GCP) guidelines. Excellent organizational, communication, and problem-solving skills, with a strong attention to detail and the ability to multitask, are essential.
The Associate Clinical Research Project Manager will assist in the planning, execution, and oversight of clinical research projects, coordinating cross-functional teams and ensuring compliance with protocols and standard operating procedures. This role involves working closely with study coordinators, investigators, and sponsor representatives to maintain regulatory compliance, including GCP guidelines. Responsibilities include assisting in the development and review of study documents, participating in study start-up activities, managing study vendors, coordinating study monitors, tracking and reporting on study progress, and contributing to the preparation of study reports and publications.
Advanced cardiac monitoring solutions provider
iRhythm Technologies focuses on cardiac monitoring solutions, with its main product being the Zio Patch, a wearable device that tracks heart rhythms for up to 14 days. This extended monitoring helps healthcare providers detect irregular heart rhythms that shorter monitoring might miss, making it especially useful for patients at risk. The company serves both patients and healthcare providers, generating revenue by selling the Zio Patch and offering data analysis services to interpret the collected heart data. iRhythm aims to improve patient outcomes and streamline healthcare workflows in the cardiac health sector.