Clinical Research Coordinator 2 - Aventura/Sole Mia

University of Miami; North Miami (FL); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator 2 to join their dynamic team at Aventura/Sole Mia. This role is pivotal in facilitating clinical research studies, ensuring participant safety, and adhering to regulatory guidelines. You will coordinate various study activities, assist in participant recruitment, and maintain meticulous documentation. The position offers a collaborative environment where your contributions will directly impact the success of groundbreaking research. If you are detail-oriented and passionate about clinical research, this opportunity is perfect for you.

Benefits

Medical insurance

Dental insurance

Tuition remission

Comprehensive benefits package

Qualifications

• Bachelor’s degree required with 2+ years of relevant experience.
• Strong skills in attention to detail and confidentiality.

Responsibilities

• Assist in planning and coordinating clinical research studies.
• Perform study procedures and maintain study documentation.
• Monitor protocol implementation and ensure participant safety.

Skills

Attention to detail

Analytical skills

Confidentiality

Ability to work independently

Collaborative skills

Education

Bachelor's degree in relevant field

Job description

Clinical Research Coordinator 2 - Aventura/Sole Mia

Clinical Research Coordinator 2 - Aventura/Sole Mia

Apply locations UHealth SoLe Mia time type Full time posted on Posted 3 Days Ago job requisition id R100085912

The University of Miami Health System at Aventura Sole Mia has an exciting opportunity for a full-time Clinical Research Coordinator 2.

The Sylvester Comprehensive Cancer Center has an exciting opportunity for Clinical Research Coordinator 2 at Aventura Sole Mia. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.

CORE JOB FUNCTIONS

• 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.

MINIMUM QUALIFICATIONS:

• Bachelor’s degree in relevant field required
• Minimum 2 years of relevant experience

KSA

• 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.
• Ability to work independently and/or in a collaborative environment.
• Commitment to the University’s core values.

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 - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.