Assoc Clinical Data Spec - Exempt

This a Full Remote job, the offer is available from: Minnesota (USA) We are seeking a skilled professional to join our team as an Assoc Clinical Data Specialist (Cardiac Technician). The ideal candidate will have a strong background in cardiac monitoring and analysis, with a focus on ECG interpretation and pacemaker/ICD management. This is a remote position requiring 40 hours per week, with the possibility of a flexible schedule for highly experienced candidates. Must Have Qualifications: • 12 Lead ECG Interpretation • Analysis of EGMs and measured data • Management of clinical testing of pacemaker/ICD • CRAT/ ECG Technician certification • ECG analysis Top Needs: • CCI CRAT or CCT certified • 3 years of Pacemaker/ICD experience • 2 years of medical device or cardiac experience Essential Responsibilities: • Identify normal and abnormal findings during basic device interrogations, ECGs, or EGMs, including ICMs, pacemakers, ICDs, and cardiac resynchronization devices. • Review and analyze data with research groups and clinical data teams to assist research members in study protocols. Education Required: Minimum Associate Degree required. Bachelor's degree in Health Sciences, Biology, or a related field preferred. Years of Experience Required: 2-5 years related work experience required in cardiac monitoring and analysis. Additional Responsibilities: • Collaborate with various departments on the design, documentation, testing, and implementation of clinical data collection studies and clinical database review. • Design and implement clinical protocols and data collection systems. • Develop systems for organizing data to analyze, identify, and report data and trends. • Manage data management issues by reviewing protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives. • Develop data quality plans. • Provide early strategic input into protocol design focused on data management issues. • Review and resolve data discrepancies for standardized data validation systems and procedures. • Prepare reports of clinical trial studies for internal validation and cross-validation studies. Specialist Career Stream: This role is typically an individual contributor with responsibility in a professional discipline or specialty. The individual will deliver and/or manage projects assigned and work with other stakeholders to achieve desired results. The majority of time is spent delivering and overseeing the projects – from design to implementation – while adhering to policies, using specialized knowledge and skills normally acquired through advanced education. Differentiating Factors: • Autonomy: Entry-level individual contributor on a project or work team. Works with close supervision. • Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities. • Innovation and Complexity: Identifies, defines, and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems. • Communication and Influence: Communicates primarily with internal contacts within the immediate group. Contacts others to gather, confirm, and convey information. • Leadership and Talent Management: N/A – job at this level is focused on self-development. Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. A Baccalaureate degree is required, or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A), with 0 years of experience required. This offer from "LanceSoft, Inc." has been enriched by Jobgether.com and got a 72% flex score.