Senior Clinical Research Coordinator II – Infectious Disease Trials

Johns Hopkins University; Baltimore (MD); Hybrid; USD 49,000 - 86,000; Full time

Job summary

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator II to provide administrative, regulatory, and operational support for studies including RCCS, IN-STEP, and SENTINEL.

You will collaborate with investigators to ensure feasible protocols, craft consent forms, and prepare IRB submissions while coordinating budgets and referrals. The role requires a Bachelor's degree and five years of related experience; a Master's degree may substitute for some experience.

Qualifications

• Bachelor's Degree required; five years of related experience preferred.
• Master's Degree may substitute required experience per policy.

Responsibilities

• Collaborate with PI and study team to ensure feasibility of protocol/study design.
• Develop standard operating procedures and data collection forms from protocols.
• Develop consent forms for studies based on protocols.
• Prepare materials for IRB submissions and regulatory follow-up.
• Train and oversee research data management and regulatory issues.
• Coordinate with sponsors to determine feasible groups given population, resources, and costs.
• Work with the finance team to develop study budgets and ensure costs are included.
• Ensure PRA is completed and followed when required; track milestones for invoicing.
• Initiate activities to increase referrals and accruals to clinical trials.
• Develop, test, and evaluate data collection manuals and coding structures.
• Organize and quality control study data across sites.
• Oversee data collection at single or multiple sites; conduct self-audits/as needed.
• May supervise day-to-day activities and train staff.

Education

Bachelor's Degree in a related field

Master's Degree in a related field

Job description

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator II to provide administrative, regulatory, and operational support for studies including RCCS, IN-STEP, and SENTINEL.

You will collaborate with investigators to ensure feasible protocols, craft consent forms, and prepare IRB submissions while coordinating budgets and referrals. The role requires a Bachelor's degree and five years of related experience; a Master's degree may substitute for some experience.