Assoc Clinical Data Spec - Exempt

Assoc Clinical Data Specialist (Cardiac Technician)

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.