Clinical Studies Spt Coord II.

Posted:
2/19/2026, 4:57:07 AM

Location(s):
Bogota, Capital District, Colombia ⋅ Bogota, Bogota, Capital District, Colombia

Experience Level(s):
Junior ⋅ Mid Level

Field(s):
Medical, Clinical & Veterinary

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.
The role supports clinical studies by ensuring accurate, complete, and timely collection of study data. This role involves coordinating data entry, verifying case report forms, maintaining study documentation, and assisting in the management of study files in compliance with protocol and regulatory standards. The position plays a vital part in maintaining the integrity and quality of clinical research data. This position will be a Remote position in Bogotá

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

  • Support clinical studies by executing and maintaining one or more of the following areas
  • Data coordination- actively participate in the development and testing of case report forms, study reports, and study databases based on protocol requirements
  • Ensure 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
  • Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents
  • Assist with periodic audits of clinical study files for completeness and accuracy

Required Knowledge and Experience:

  • Bachelor’s degree is advantageous
  • One to two years of experience supporting clinical research, data coordination or document management is preferred
  • Advanced communication skills (written & verbal)
  • Knowledge of Microsoft Office Applications (Word, Excel, Access, PowerPoint, Outlook)
  • Fluent in English

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. 

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.
 

 

 

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

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here