About this role
Under direct Supervision, the Clinical Research Assistant – Associate is responsible for accurately and promptly entering patient data from clinical trials into sponsor or local databases. They must locate the required information in patient records, ensure data accuracy and integrity, and collaborate with the research team to resolve data queries. Additionally, they coordinate monitoring visits with study monitors and participate in study teleconferences with sponsors and clinical research organizations to maintain consistent communication and information flow.
Education: Bachelors degree is required.
- Ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
- Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
- Demonstrated ability to monitor important and complex projects concurrently.
- Familiarity with medical terminology and clinical documentation practices.
- Understanding of basic biostatistics and clinical data interpretation.
- Strong attention to detail and data accuracy.
- Excellent organizational and time management skills.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook) and database systems.
- Ability to interact professionally with patients, sponsors, monitors, and staff.
- Effective written and verbal communication skills.
- Demonstrated knowledge of standard clinical research practices, oncology care procedures, and data management principles.