Clinical Research Coordinator
Current• Patient recruitment for clinical research: recruitment plans and informed consent.• Management of Clinical Data, CRFs (case report forms), and various research projects.• Coordination between clinical and research teams.• Assisting in skin biopsy procedures.• Preparation of Masterfile: writing Masterlog, protocol amendments, SOPs, Task Delegation Log, and others.• Coordination of industry-funded projects and updates meetings with the companies.• Analysis, graphing, and presentation of descriptive analyses of our patient cohort.Part of my work included research associate responsibilities:• Worked on characterizing immune cells involved in eczema, using patient’s skin and blood specimens, through techniques such as flow cytometry, RNAscope, and immunofluorescence.• Meeting with biostatisticians and bioinformaticians to perform complex analyses of single-cell RNA sequencing datasets and our own Hiplex-RNAscope analysis.• Performing and writing systematic reviews.• Writing protocols (SOPs and WI).• Managing volunteering medical students.• Mentoring a master’s student and managing medical students.• Preparation of PowerPoint presentations for collaboration meetings.• Participation in the execution of industry-funded projects.
