Assoc Clinical Data Spec - Exempt

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.