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University of Miami · 1 day ago

Clinical Research Coordinator 2

Miami, FL

Full-time

Onsite

Entry, Mid Level

2+ years exp

The University of Miami is an academic medical center providing leading-edge patient care and medical education. They are seeking a Clinical Research Coordinator 2 to assist in participant recruitment, perform study procedures, and ensure adherence to clinical research protocols.

Higher Education

H1B Sponsor Likely

Responsibilities

Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility

Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols

Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations

Maintains study binders and filings according to protocol requirements, UM and department policy

Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator

Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations

Assists in implementing protocol amendments under direct supervision of the Principal Investigator

Assists with study orientation and protocol related in-services to research team and clinical staff

Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule

Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments

Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews

Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc

Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies

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

Performs screening/recruitment, obtains informed consent process and completes eligibility verification for applicable studies

Establishes and maintains communication with study participants, inter- and intra- departmental study team members, health care providers, sponsors and regulatory entities

Ensures study protocol adherence, including completion of protocol specific procedures and documentation

Maintains screening, enrollment, deviation, delegation of authority and other sponsor and/or protocol specific logs

Enters data onto case report forms and electronic data capture systems in accordance with ALCOA-C+ principles

Collects, processes, ships and tracks biological specimens following study protocol and regulatory guidelines

Reviews consent forms, sample collection tracking forms and clinical data to ensure quality and accuracy

Addresses data inconsistencies and provides responses to queries in a timely manner

Maintains inventory of study supplies and procures collection kits/supplies in anticipation of future needs

Attends research meetings with investigators, study team and site disease group; participates in scientific and clinical discussions relevant to the studies supported

Qualification

Clinical research experienceData collectionRecordingProtocol adherenceCCRC certificationPhlebotomy certificationBilingual (English/Spanish)PrioritizeAttention to detailConfidential information handlingIndependent workCollaborative environment

Required

Bachelor's degree in relevant field

Minimum 2 Years Of Relevant Experience

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

Preferred

CCRC and phlebotomy certifications preferred

Bilingual (English/Spanish) preferred

Benefits

Medical

Dental

Tuition remission

And more

Company

University of Miami

Glassdoor3.9

At UM you'll join a diverse and energized academic community.

Founded in 1925

Coral Gables, fl, US

5001-10000 employees

http://miami.edu

H1B Sponsorship

University of Miami has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2025 (208)

2024 (151)

2023 (149)

2022 (121)

2021 (95)

2020 (114)