
Clinical Studies Support Coordinator
At Medtronic, we are looking for an experienced and detail-oriented Clinical Studies Support Coordinator to join our team. We are looking for someone who is passionate about clinical research and has a knack for problem-solving. As a Clinical Studies Support Coordinator, you will be the critical link between our clinical studies team and research partners. You will be responsible for managing and coordinating all aspects of clinical studies operations.To be successful in this role, you should have a Bachelor’s degree in a related field and a minimum of 3 years of experience in clinical research or a related field. You will need to demonstrate excellent organizational and communication skills, as well as a deep understanding of the clinical research process. You should also have a keen eye for detail and be comfortable working with data and analytics. Additionally, you should have experience with project management tools. If you are passionate about making an impact in the field of clinical research and have the qualifications we are looking for, we would love to hear from you.
Responsibilities:
- Manage and coordinate all aspects of clinical studies operations.
- Demonstrate excellent organizational and communication skills.
- Deep understanding of the clinical research process.
- Keen eye for detail and comfort working with data and analytics.
- Experience with project management tools.
- Collaborate with clinical studies team and research partners.
- Develop and implement strategies to improve clinical studies operations.
- Monitor and report progress of clinical studies operations.
- Ensure compliance with applicable regulations and standards.
- Maintain accurate records and document actions taken.
Excellent Organizational Skills
Ability To Prioritize And Manage Multiple Tasks
Strong Attention To Detail
Excellent Interpersonal And Communication Skills
Bachelor's Degree Or Equivalent Experience
Ability To Maintain Confidential Information
Knowledge Of Clinical Research Studies And Documentation Requirements
High Level Of Computer Proficiency
Documentation
Quality Assurance
Project Management
Data Entry
Communication
Problem Solving
Database Management
Technical Writing
Record keeping
Regulatory compliance
Administrative support
Patient relations
Clinical Trials
Protocols
Research Assistance
Communication
Leadership
Problem Solving
Time management
Interpersonal Skills
creativity
Organization
flexibility
Teamwork
Adaptability
According to JobzMall, the average salary range for a Clinical Studies Support Coordinator in Fridley, MN, USA is between $51,085 and $77,812 per year. The salary range depends on factors such as the experience of the candidate, the size of the organization, and the industry.
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Medtronic plc is the world's largest medical device company that generates the majority of its sales and profits from the US healthcare system and is headquartered on the island of Ireland.

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