Clinical Research Data Specialist 2
- Location
- Miami, FL
- Listed
- 5 days ago
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 University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Data Specialist 2 to work at the UHealth campus in Miami, Fl.
Core Summary
The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance with department standard operating procedures, with limited supervision from the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist 2 is responsible for accurate and timely data compilation, registration, and submission, ongoing monitoring of protocol compliance, adherence to SOPs, and all applicable regulations and guidelines.
Core Job Functions
- Reviews and independently abstracts medical records for research participants across multiple assigned studies with moderate complexity.
- Extracts, validates, and enters clinical and research data from electronic medical records and source documents into paper-based or electronic data capture systems.
- Ensures data accuracy, completeness, and timeliness in accordance with protocol requirements and study timelines.
- Resolves and responds to data clarifications (i.e., data queries) independently, escalating complex issues as needed.
- Coordinates and supports routine monitoring visits by preparing participant cases, documentation, and source data, and by addressing post-visit follow-up items.
- Addresses and closes clinical and data discrepancies identified in monitoring reports prior to subsequent monitoring visits.
- Develops and maintains study-specific source documentation and worksheets aligned with protocol and sponsor requirements.
- Maintains proactive communication with information services, providers, and research staff to support ongoing data collection and issue resolution.
- Documents and tracks study-specific activities, including monitoring visits, enrollments, protocol amendments, and safety reports, within the clinical trial management system in real time.
- Ensures all study documentation meets internal, external, sponsor, and regulatory requirements in accordance with protocol guidelines.
- Maintains and audits study-related logs and tracking tools to support compliance and inspection readiness.
- Participates in site initiation visits, monitoring visits, and PI oversight or study team meetings, contributing data-related insight as appropriate.
- Supports and collaborates with multidisciplinary research teams to facilitate study execution and data integrity.
- Maintains organized, audit-ready study binders and regulatory files and contributes to an efficient, compliant, and collaborative research environment.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
Additional information
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: High School Diploma or equivalent/relevant experience, certification or license
- Experience: Minimum 2 years of relevant experience required
Knowledge, Skills and Abilities
- 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.
Pay and benefits
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.
Job Status: Full time
Employee Type: Staff
Equal opportunity and legal notices
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
From UMiami's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Clinical Research Data Specialist 2 job at UMiami located?
This Clinical Research Data Specialist 2 position at UMiami is located in Miami, FL. Always check UMiami's application page for specific state eligibility or relocation policies.
How do I apply for the Clinical Research Data Specialist 2 position at UMiami?
This listing links directly to UMiami's Workday application page. You can apply directly on UMiami's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.