Sr. Clinical Research Coordinator (Division of Cardiology)

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

Job summary

The Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee complex clinical studies and implement research protocols. The role involves ensuring compliance with regulations, developing standard operating procedures, and leading participant recruitment strategies.

Applicants should have a Bachelor's Degree in a related field and three years of relevant experience. This is a full-time hybrid position with a starting salary range of $41,300 - $72,300 annually.

Qualifications

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

Responsibilities

• Oversee day-to-day activities of complex clinical studies.
• Develop standard operating procedures and consent forms.
• Ensure compliance with protocol and regulations.
• Participate in study budget development.
• Set up and validate recruitment strategies.

Skills

Operational feasibility assessment

Standard operating procedures development

Data collection and validity

Budget development

Regulatory compliance

Recruitment strategy

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., in-patient 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