What are the responsibilities and job description for the Senior Clinical Research Data Specialist position at Temple Health – Temple University Health System?
Category
Research & Science
Job Location
333 Cottman Avenue, Philadelphia, Pennsylvania, United States
Tracking Code
265157
Weekly Hours
40.00
Schedule
Full-Time
Shift
Day Shift
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
5 years experience in related clinical research role Required
Research & Science
Job Location
333 Cottman Avenue, Philadelphia, Pennsylvania, United States
Tracking Code
265157
Weekly Hours
40.00
Schedule
Full-Time
Shift
Day Shift
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
5 years experience in related clinical research role Required