Clinical Research Coordinator 1 Job at The University of Miami, Miami, FL

V2ZiRDFJdXdMaGhZMVNsVkpmdmVWVUZ0SHc9PQ==
  • The University of Miami
  • Miami, FL

Job Description

Current Employees:

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.

The department of Medicine has an exciting opportunity for a full-time Clinical Research Coordinator 1 to work onsite on the UHealth campus. 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 JOB FUNCTIONS
  • 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
  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
  • Assist in participant recruitment and retention activities, screening potential study subjects for eligibility.
  • Collection of Inform Consent including proper documentation of the discussion process following GCP and research regulations.
  • Collection, processing, packaging, and shipment of Specimens according to protocol.
  • Maintain study binders and filings according to protocol requirements.
  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Perform other duties as assigned by the PI.

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
  • Bachelor's degree in relevant field required
  • Minimum 1 year of relevant experience
  • Bilingual (English and Spanish) preferred.

Knowledge, 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.

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:
Staff

Job Tags

Full time, Temporary work, Local area, Worldwide, Night shift, Weekend work, Afternoon shift,

Similar Jobs

Fantastic Sams Cut & Color SW Florida

Cosmetologist Cape- Where Talent, Training & Teamwork Thrive Job at Fantastic Sams Cut & Color SW Florida

 ...our clients. Experience : While experience is preferred, we are open to training individuals with a strong passion for hair and beauty. Apply Today! Join our team and become a part of a growing family business with a commitment to excellence. We are excited to... 

Keller Executive Search International

Commercial Real Estate Legal Assistant #1510 Job at Keller Executive Search International

 ...Keller Executive Search is seeking a detail-oriented and proactive Commercial Real Estate Legal Assistant to join a prestigious law firm in Tallahassee, Florida. In this pivotal role, you will support attorneys specializing in commercial real estate transactions, ensuring... 

Agape Hospice

Home Care Caregiver - CNA's WANTED Job at Agape Hospice

 ...there is pain, solutions where there are challenges, and peace where there is chaos in the lives of our patients and their loved ones. Hospice is not about dying, rather it is about living and maximizing the quality of life that a person has remaining. It recognizes death... 

ICON

Clinical Research Associate Job at ICON

 ...) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment...  ...development We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and... 

Abbott

Clinical Research Associate I Job at Abbott

 ...The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical...  ...preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate education and experience....