Clinical Research Coordinator 1

Socket.dev; Miami (FL); On-site; USD 52,000 - 66,000; Full time

Job summary

The University of Miami/UHealth, Department of Public Health, seeks a temporary full-time Clinical Research Coordinator 1 in Miami, FL. The role supports entry-level clinical research with responsibilities in data management and implementing protocols, handling simple study timelines and coordination under supervision.

Core duties include chart reviews, data collection, scheduling, and assisting in adverse event reporting.

Qualifications

• Bachelor's degree in relevant field required.
• Minimum 1 year of relevant experience.
• Active phlebotomy certification.
• Active driving license.
• Learning agility: adapt to changing priorities and work demands.
• Teamwork: collaborate with others in a team.
• Technical proficiency: office software and related applications.
• Strong written and verbal communication for interacting with colleagues and stakeholders.

Responsibilities

• Perform chart review/pre-screening for eligibility and coordinate simple protocols.
• Coordinate routine study activities including data collection, timelines, appointments, and visits.
• Perform moderate to complex research tests under supervision.
• Follow instructions for operating clinical research equipment and solve operational problems.
• Observe and report adverse events to PI/supervisor.
• Address protocol deviations and unanticipated occurrences.
• Follow regulatory requirements from applicable bodies.
• Maintain study regulatory binders and training in safety and research ethics.

Skills

Learning Agility

Teamwork

Technical Proficiency

Communication

Education

Bachelor's degree in relevant field

Tools

Phlebotomy certification

Driving license

Job description

The University of Miami/UHealth, Department of Public Health, has an exciting opportunity for a temporary full time Clinical Research Coordinator 1 to work in Miami, FL.

The Clinical Research Coordinator 1 serves as an entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible 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.

Department Specific Functions:

• Project coordination skills, including planning project tasks, and overseeing project progress, data collection, surveillance, systematically documentation of project records, storage and processing of environmental and laboratory specimen.
• Must have an active driving license and willing to travel in/around Miami area.
• Ability to effectively communicate with clinicians, researchers and patients.

Core Qualifications:

• Bachelor’s degree in relevant field required. Preferred education in nursing or biochemistry or health related field.
• Minimum 1 year of relevant experience required.
• Active phlebotomy certification.
• Active driving license.
• Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
• Teamwork: Ability to work collaboratively with others and contribute to a team environment.
• Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
• Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

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 time

Employee Type:

Temporary