ProPAC Tools & Services Interview Questions and Answers

I have conducted interviews with study participants and completed data analysis for the close out phase.

• Conducted interviews with study participants

• Completed data analysis for close out phase

I have extensive experience in source writing for clinical research studies.

• I have written source documents such as case report forms, study protocols, and informed consent forms.

• I ensure accuracy, clarity, and compliance with regulatory guidelines in all source writing.

• I have experience in collaborating with cross-functional teams to develop and review source documents.

• I am proficient in using electronic data capture systems for source writing and data management.

Proficient in using EDC tools for data collection and management in clinical research.

• Experience with various EDC systems such as Medidata Rave, Oracle InForm, and REDCap

• Ability to design electronic case report forms (eCRFs) and manage data entry

• Knowledge of data validation checks and discrepancy management

• Experience in generating reports and analyzing data for clinical trials