Found Description
Responsibilities
- Identify and screen potential study participants based on inclusion and exclusion criteria as outlined in the study protocol
- Obtain informed consent from participants ensuring they fully understand the study’s purpose, procedures, and potential risks and benefits
- Assist in data collection and ensure accurate entry of study data into electronic data capture systems and clinical databases
- Maintain detailed and organized records of study‑related activities including patient information, consent forms, and other relevant documents
- Conduct regular data quality checks to ensure accuracy and completeness of collected data
- Schedule study visits and follow‑ups with participants, coordinating with clinical staff as needed
- Provide support to study participants throughout the study process, addressing any questions or concerns as needed
- Follow study protocols and standard operating procedures (SOPs)...