Clinical Research Data Specialist II (Phase 1)

Temple-Health; Philadelphia (Philadelphia County); On-site; USD 70,000 - 100,000; Full time

Job summary

Temple-Health in Philadelphia is seeking a Clinical Research Data Specialist II (Phase 1) to support data collection, analysis and reporting for oncology trials.

You will extract data from source documents, respond to data queries, organize clinical data, participate in study initiation and monitoring visits onsite. Flexibility in schedule to ensure study responsibilities is preferred.

Qualifications

• Bachelor's degree required; combination of relevant education and experience may be considered in lieu of degree
• 2 years of 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 organize clinical data
• Participate in study initiation meetings and study monitoring visits onsite
• Interact with investigators, healthcare team and participants to support trial conduct

Skills

Data extraction

Data analysis

Clinical collaboration

Education

Bachelor's Degree

Experience in clinical research

Job description

Clinical Research Data Specialist II (Phase 1)

333 Cottman Avenue, Philadelphia, Pennsylvania, United States

Tracking Code

265238

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
• Combination of relevant education and experience may be considered in lieu of degree experience in related clinical research role Required

Experience

• 2 years experience in related clinical research role Required