Skip to main content
Loading
loadingbar
Loading, Please wait..!!

Clinical Research Coordinator 1

  • Clinical Research Coordinator 1 job type Posted on: Nov 11, 2026
  • Clinical Research Coordinator 1 experience level University of Miami
  • Clinical Research Coordinator 1 employment type Miami, Florida
  • Clinical Research Coordinator 1 employment type Onsite
  • Clinical Research Coordinator 1 salary Full-time

Point Apply Here APPLY LATER

Curious about compensation?

Explore the historical salary trends, average pay, and estimated compensation for Clinical Research Coordinator 1 roles in Florida.

View Salary Guide →

Job Title :

Clinical Research Coordinator 1

Job Type :

Full-Time

Job Location :

Miami Florida United States

Remote :

No

Jobcon Logo Job Description :

Clinical Research Coordinator 1The Clinical Translational Research Site is currently seeking a full-time Clinical Research Coordinator 1 to work in Miami.The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.Core Responsibilities:Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.Performs moderate to complex research tests/experiments and adapts procedures for quality improvement under supervision.Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.Knows the contents and maintenance of study-specific clinical research regulatory binders.Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.Adheres to University and unit-level policies and procedures and safeguards University assets.This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.Core Qualifications:Education: Bachelor's degree in relevant fieldExperience: Minimum 1 year of relevant experienceKnowledge, Skills and Attitudes:Skill in completing assignments accurately and with attention to detail.Ability to analyze, organize and prioritize work under pressure while meeting deadlines.Ability to process and handle confidential information with discretion.Ability to work evenings, nights, and weekends as necessary.Commitment to the University's core values.Ability to work independently and/or in a collaborative environment.The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.Job Status: Full timeEmployee Type: Staff

Jobcon Logo Position Details

Posted:

Nov 11, 2026

Reference Number:

19792_U-130764921114

Employment:

Full-time

City:

Miami

Job Origin:

APPCAST_CPC

Share this job:

  • linkedin

Jobcon Logo
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Clinical Research Coordinator 1    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Clinical Research Coordinator 1The Clinical Translational Research Site is currently seeking a full-time Clinical Research Coordinator 1 to work in Miami.The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.Core Responsibilities:Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.Performs moderate to complex research tests/experiments and adapts procedures for quality improvement under supervision.Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.Knows the contents and maintenance of study-specific clinical research regulatory binders.Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.Adheres to University and unit-level policies and procedures and safeguards University assets.This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.Core Qualifications:Education: Bachelor's degree in relevant fieldExperience: Minimum 1 year of relevant experienceKnowledge, Skills and Attitudes:Skill in completing assignments accurately and with attention to detail.Ability to analyze, organize and prioritize work under pressure while meeting deadlines.Ability to process and handle confidential information with discretion.Ability to work evenings, nights, and weekends as necessary.Commitment to the University's core values.Ability to work independently and/or in a collaborative environment.The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.Job Status: Full timeEmployee Type: Staff

Loading
Please wait..!!