Senior Clinical Research Data Specialist

Temple Health – Temple University Health System; Philadelphia (Philadelphia County); On-site; USD 70,000 - 90,000; Full time

Job summary

Temple Health – Temple University Health System is seeking a Clinical Research Data Specialist to support data collection, analysis and reporting for oncology trials in Phase I–III. The role works with a Clinical Research Nurse/Coordinator to ensure accurate data compilation and timely submissions onsite at 333 Cottman Avenue in Philadelphia.

The ideal candidate has a Bachelor's degree and at least 5 years in clinical research, with strong data management and collaboration skills to support

Qualifications

• Bachelor's Degree Required or combination of relevant education and experience may be considered in lieu of degree.
• 5 years experience in related clinical research role Required.

Responsibilities

• Extract data from source documents to complete case report forms for oncology trials.
• Respond to data queries and gather/organize clinical data.
• Participate in study initiation meetings and monitoring visits onsite.
• Interact with investigators, healthcare team and participants to support trials.
• Maintain flexible schedule to cover study responsibilities.

Skills

Data collection

Data analysis

Reporting

Education

Bachelor's Degree

Job description

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

Responsibilities

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