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University of Miami

Clinical Research Data Specialist

University of Miami, Miami, Florida, us, 33222

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Core Job Summary The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Clinical Research Data Specialist to work at the UHealth campus in Miami, FL. The Clinical Research Data Specialist assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures, under the supervision of the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable regulations and guidelines.

Core Job Functions

Extracts clinical data and research data from electronic medical records and other sources and enters this data in the clinical paper-based or electronic data capture system for each assigned study.

Manages a workload of studies commensurate with level of experience.

Answers data clarifications (i.e., data queries) for each study.

Schedules and meets with study monitors and assures patient cases are ready for each monitor visit and items are addressed after each monitoring visit.

Develops source data worksheets specific to each assigned study.

Assures clinical issues from monitoring reports are addressed and closed out before the next monitoring visit.

Assures all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.

Maintains logs (e.g., TAS submissions, Velos) in a timely manner according to department SOPs.

Participates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required.

Assists multidisciplinary team in research activities.

Maintains study binders and filings according to protocol requirements and department policy.

Maintains screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs.

Compiles patient data for Investigator review to determine patient eligibility for protocol enrollment.

Ensures work environment is organized and functions efficiently, and demonstrates a professional practice to support delivery of care.

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:

No previous experience required.

Knowledge, Skills and Abilities:

Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities.

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.

Job Status: Full time; Employee Type: Staff; Pay Grade: A6.

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.

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