Sr. Clinical Research Coordinator (Division of Cardiology)

Johns Hopkins University; Baltimore (MD); On-site; USD 41,300 - 72,300; Full time

Job summary

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee daily activities for complex clinical studies. This role requires developing protocol compliance, managing study data, and contributing to budget formulation.

The ideal candidate will have a Bachelor’s Degree and at least three years of related experience. Responsibilities include ensuring regulatory compliance and developing recruitment strategies for participants in clinical trials. A Master’s Degree is preferred.

Qualifications

• Bachelor's Degree in a related field.
• Three years of related experience required.
• Master's Degree preferred.

Responsibilities

• Oversee daily activities of clinical studies.
• Ensure operational feasibility of study designs.
• Develop consent forms and materials for IRB submission.
• Contribute to study budget and participant recruitment strategies.

Skills

Clinical protocol development

Data collection and analysis

Budget management

Regulatory compliance

Education

Bachelor's Degree in a related field

Job description

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a Sr. Clinical Research Coordinator who will oversee the day-to-day activities of a single complex study (e.g., inpatient study, translational research involving clinics and labs, participant accrual at multiple sites, study for which Hopkins is a coordinating center) or multiple clinical research studies and makes independent decisions that impact the conduct of the research. Assists in goal setting and creating implementation plans. Contributes to budget formulation, communications, and data systems.

Specific Duties & Responsibilities

• Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design.
• Develop standard operating procedures and data collection forms from protocol(s).
• Develop consent form(s) for clinical trials based on protocol(s).
• Prepare materials for submission to IRB.
• Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services.
• Ensure compliance with all protocols, procedures, and applicable regulations.
• Participate in developing the study budget.
• Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies.
• Set up a data collection system and ensure the 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 and recommend changes to protocol operations based on results and goals.
• Conduct literature searches to provide background information.
• Abstract and index information based on knowledge of subject matter.
• Other duties as assigned.

Minimum Qualifications

• Bachelor's Degree in a related field.
• Three years of related experience.
• Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Preferred Qualifications

• Master's Degree in a related field.

Classified Title: Sr. Clinical Research Coordinator
Role/Level/Range: ACRP/03/MB
Starting Salary Range: $41,300 - $72,300 Annually ($45,000 targeted; Commensurate w/exp.)
Employee group: Full Time
Schedule: Mon - Fri 8 - 4:30
FLSA Status: Exempt
Location: Hybrid/School of Medicine Campus
Department name: SOM DOM Cardiology
Personnel area: School of Medicine