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A Day in the Life

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The Clinical Research function supports the generation, management, and execution of clinical evidence across the Latin America region. This team partners with investigators, research institutions, regulatory stakeholders, and internal cross-functional teams to support clinical studies, investigator-sponsored research activities, and clinical supply operations. The role also contributes to study execution through investigational product management, clinical systems administration, and SAP-based supply processes.
This position is based in Bogotá, Colombia. The role follows a Flex work model and supports regional clinical research activities across Latin America. Travel is not expected as part of this role.

Responsibilities may include the following and other duties may be assigned:

• Support oversight and execution of investigator-sponsored research and clinical study activities across the Latin America region
• Coordinate operational aspects of clinical studies in compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable country regulations
• Manage investigator and research site relationships and support collaboration with external research partners and institutions
• Support investigational product and clinical supply activities, including inventory management, shipment tracking, distribution, and reconciliation
• Coordinate importation, customs clearance, and logistics activities for clinical trial materials with internal and external stakeholders
• Perform SAP transactions related to study supply orders, inventory movements, material tracking, purchase requisitions, and stock transfers
• Maintain study documentation, inventory records, clinical systems, dashboards, and tracking tools including Clinical Trial Management Systems (CTMS)
• Collect and communicate investigator feedback, regional research insights, and operational risks to support clinical research objectives

 

Required Qualifications

• Bachelor's degree and 1+ years of clinical research experience in pharmaceutical, medical device, hospital, epidemiology, nursing, or healthcare research environments
• Advanced English proficiency (minimum B2 level required)
• Experience supporting clinical studies and clinical research documentation
• Experience working with Good Clinical Practice (GCP) requirements and clinical research processes
• Experience using SAP for operational, inventory, supply chain, or study support activities

Preferred Qualifications

• Experience supporting investigator-sponsored research programs
• Experience with investigational product management, clinical supply operations, or clinical trial logistics
• Experience using Clinical Trial Management Systems (CTMS) or other clinical research systems
• Portuguese language proficiency
• Experience collaborating with cross-functional teams across multiple countries within a regional organization

 

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

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Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. 

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If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected]. 

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 

 

 

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This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).