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Clinical Research Data Specialist 2

The Miami Project to Cure Paralysis1,735 open roles

Where
Miami, FL
Work mode
Hybrid
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Your applicationOpen nowClinical Research Data Specialist 2The Miami Project to Cure Paralysis · Miami, FL

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on The Miami Project to Cure Paralysis's own form.

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The clock on this job

Early applications get read.

9.4% of postings close within 7 days. Measured by our own scanner across the market. The Miami Project to Cure Paralysis postings stay open a median of 28 days.

Share of postings closed within
  1. 1.8%1 day
  2. 3.9%3 days
  3. 9.4%7 days
  4. 15.5%14 days
  5. 33.8%30 days
This job: posted today

The Miami Project to Cure Paralysis median: 28 days open

The posting

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 medical campus in Miami, Florida.

CORE JOB 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

1. Reviews and independently abstracts medical records for research participants across multiple assigned

studies with moderate complexity.

2. Extracts, validates, and enters clinical and research data from electronic medical records and source

documents into paper‑based or electronic data capture systems.

3. Ensures data accuracy, completeness, and timeliness in accordance with protocol requirements and study

timelines.

4. Resolves and responds to data clarifications (i.e., data queries) independently, escalating complex issues as

needed.

5. Coordinates and supports routine monitoring visits by preparing participant cases, documentation, and

source data, and by addressing post‑visit follow‑up items.

6. Addresses and closes clinical and data discrepancies identified in monitoring reports prior to subsequent

monitoring visits.

7. Develops and maintains study‑specific source documentation and worksheets aligned with protocol and

sponsor requirements.

8. Maintains proactive communication with information services, providers, and research staff to support

ongoing data collection and issue resolution.

9. Documents and tracks study‑specific activities, including monitoring visits, enrollments, protocol

amendments, and safety reports, within the clinical trial management system in real time.

10. Ensures all study documentation meets internal, external, sponsor, and regulatory requirements in

accordance with protocol guidelines.

11. Maintains and audits study‑related logs and tracking tools to support compliance and inspection readiness.

12. Participates in site initiation visits, monitoring visits, and PI oversight or study team meetings, contributing

data‑related insight as appropriate.

13. Supports and collaborates with multidisciplinary research teams to facilitate study execution and data

integrity.

14. Maintains organized, audit‑ready study binders and regulatory files and contributes to an efficient,

compliant, and collaborative research environment.

15. Adheres to University and unit-level policies and procedures and safeguards University assets.

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.

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

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