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Clinical Research Data Specialist (Phase 1) at Temple Health System

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Feb, 26

Salary

0.0

Posted On

19 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Collection, Data Analysis, Data Reporting, Case Report Forms, Data Queries, Clinical Trials, Study Monitoring, Oncology Trials, Collaboration, Communication, Organizational Skills, Flexibility, Meeting Participation, Initiation Meetings, Healthcare Team Interaction, Research Participant Interaction

Industry

Hospitals and Health Care

Description

The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure accurate and timely delivery of data compilation and submission. Responsibilities include: extracting data from source documents to complete case report forms for oncology clinical trials, responding to data queries, gathering and organizing clinical data, participating in departmental and study related meetings, conducting study initiation meetings and participating in study monitoring visits onsite. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families, in a manner that supports the conduct of clinical trials. Flexibility in work schedule when possible must be maintained to ensure coverage of study responsibilities Education Bachelor's Degree Required or Combination of relevant education and experience may be considered in lieu of degree Required Experience General Experience in the medical or scientific field Preferred Licenses

Responsibilities

The Clinical Research Data Specialist supports data collection, analysis, and reporting for oncology trials. Responsibilities include extracting data, responding to queries, and participating in meetings related to clinical trials.