Sr. Clinical Research Coordinator (Pulmonary)
Core
Overseeing day-to-day activities of complex clinical research studies, including participant accrual, data management, and protocol compliance for pulmonary disease research.
Role type
Senior Clinical Research Coordinator
Builds
Clinical trials and research studies for disease prevention and treatment
Domain
Healthcare / Clinical Research / Pulmonology
Deliverable
client delivery
Required skills
Protocol development, Standard Operating Procedures (SOP) creation, Informed consent form development, IRB submission preparation, Study budget formulation, Participant recruitment strategy, Data collection system setup, Data quality control, Self-auditing, Literature search, Subject matter indexing
Preferred skills
Master's Degree in a related field
Technologies
Data collection systems
Responsibilities
Ensure operational feasibility of proposed protocol/study design, Develop standard operating procedures and data collection forms, Develop consent forms for clinical trials, Prepare materials for submission to IRB, Contribute to work with commercial and/or government agency sponsors, Ensure compliance with all protocols and regulations, Participate in developing the study budget, Develop and oversee implementation of recruitment strategy, Set up a data collection system and ensure validity of study data, Organize and quality control study data, Perform self-audits and/or audit other sites, Participate in study meetings and provide status updates, Conduct literature searches to provide background information, Abstract and index information based on knowledge of subject matter