Senior Clinical Research Data Specialist

Temple-Health; Philadelphia (Philadelphia County); On-site; USD 85,000 - 110,000; Full time

Job summary

Temple-Health is seeking a Senior Clinical Research Data Specialist to support data collection, analysis, and reporting for oncology trials within the Office of Clinical Research (OCR). You will collaborate with a Clinical Research Nurse/Coordinator to ensure accurate data compilation and timely submission.

The role requires 5 years of clinical research data management experience and a Bachelor's degree, with potential consideration for related education and experience in lieu of the degree.

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 clinical trials
• Respond to data queries
• Gather and organize clinical data
• Participate in departmental and study related meetings
• Conduct study initiation meetings
• Participate in study monitoring visits onsite
• Interact with the institutional investigators, other healthcare team members, service line members and research participants/families to support the conduct of clinical trials
• Flexibility in work schedule when possible must be maintained to ensure coverage of study responsibilities

Skills

Clinical data management

Data extraction

Education

Bachelor's Degree

Job description

Senior Clinical Research Data Specialist

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

• 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
• participating in study monitoring visits onsite
• 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
• 2 years experience with Clinical Research Data Management Preferred