Clinical Studies Spcialist Coordinator II

Medtronic

About The Position

Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. This role supports clinical studies by executing and maintaining areas such as data coordination and document coordination. The Office Support Career Stream focuses on individuals who provide organizational support or services, typically under supervision, with the majority of time spent delivering support services or activities.

Requirements

Requires full job knowledge of systems and procedures obtained through prior work experience or education.
Requires minimum of 2 years of relevant experience.

Nice To Haves

Established and productive individual contributor.
Works on clerical and administrative assignments that may require application of prior experience.
Works under moderate supervision, making minor adjustments to methods and processes.
Works to deliver on day-to-day objectives with direct impact on achievement of results for the job area, including moderate scheduling or customer satisfaction implications.
Work consists of tasks that are typically routine, with some deviation from standard practice.
Checks and makes minor adjustments to work methods to solve problems that are routine and typically exist in current work processes and systems.
May be required to highlight areas of concerns/problems and puts forth solutions in own job area.
Communicates typically with internal contacts within and outside of immediate team.
Obtains and provides information requiring some explanation or interpretation.
May provide guidance and assistance to new or entry level employees.

Responsibilities

Actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
May process compensation & identify and resolve compensation discrepancies.
Creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
Assists with periodic audits of clinical study files for completeness and accuracy.