• Consult with researchers to assist in developing a data management plan

• Design forms to facilitate the collection and tracking of study participant data, study drugs, biological specimens, and study procedures

• Design and coordinate field tests for data collection forms and assisting in design of certification procedures

• Assist with clinical and data coordination for research activities

• Screen, recruit, enroll and obtain informed consent for clinical trials

• Assist in managing data validation

• Query resolutions, and the reporting of data

• Conduct audit to assess quality assurance

• Perform all data processing tasks

• Enter data, verify data, identify problem data, generate queries, etc. 

• Coordinate the processing of data from various sites/centers/studies

• Conduct audit to assess quality assurance

• Develop procedures for on-site data audits 

• Summarize results of audits and write reports

• May provide functional and/or administrative supervision

• Mentor new staff under direction

• Bachelor’s degree in a health science related field

• Demonstrated experience in data entry 

• Experience working with Microsoft Office Suite

• Ability to work well both independently and in a team setting

• Excellent organizational and time-management skills, and attention to detail

• Excellent written and verbal communication skills

• Interest in pursuing clinical trials research in the area of Hematology/Oncology

• Experience in study design, database design, and/or data analysis