Medtronic

Clinical Studies Support Coordinator

Medtronic

Fridley, MN, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

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:

  1. Manage and coordinate all aspects of clinical studies operations.
  2. Demonstrate excellent organizational and communication skills.
  3. Deep understanding of the clinical research process.
  4. Keen eye for detail and comfort working with data and analytics.
  5. Experience with project management tools.
  6. Collaborate with clinical studies team and research partners.
  7. Develop and implement strategies to improve clinical studies operations.
  8. Monitor and report progress of clinical studies operations.
  9. Ensure compliance with applicable regulations and standards.
  10. Maintain accurate records and document actions taken.
Where is this job?
This job is located at Fridley, MN, USA
Job Qualifications
  • 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

Required Skills
  • 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

Soft Skills
  • Communication

  • Leadership

  • Problem Solving

  • Time management

  • Interpersonal Skills

  • creativity

  • Organization

  • flexibility

  • Teamwork

  • Adaptability

Compensation

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.

Additional Information
Medtronic is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedSeptember 27th, 2023
Apply BeforeMay 22nd, 2025
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About Medtronic

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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