Sr. Clinical Research Coordinator (Psychiatry and Behavioral Sciences)

John Hopkin’s University; Baltimore (MD); Sur place; USD 42 000 - 74 000; Plein temps

Résumé du poste

Johns Hopkins University seeks a Sr. Clinical Research Coordinator to oversee day-to-day activities of a single complex study or multiple studies, coordinating across clinics and labs, and ensuring protocol compliance and participant recruitment.

Minimum qualifications include a Bachelor's degree and 3 years of related experience; a Master's degree is preferred. The role is based at Johns Hopkins Bayview with standard M-F hours and exempt status.

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.

Responsabilités

• Assist Principal Investigator or more senior 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 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.
• Oversee collection and shipping of blood to national repository.
• Conduct comprehensive clinical and cognitive assessments of research participants in accordance with study protocols and standardized procedures.

Connaissances

Budget Management

Clinical Research ParticipantRecruitm

Clinical Study Design

Clinical Trial Management System

Data Management and Analysis

Data Collection and Reporting

Good Clinical Practices

Interpersonal Skills

Project Management

Regulatory Compliance

Report Writing

Formation

Bachelor's Degree

Master's Degree

Description du poste

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. Bayview Geriatric & Neuropsychiatry is seeking a Sr. Clinical Research Coordinator oversees 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.

In addition to the duties described above

• Oversee collection and shipping of blood to national repository.
• Conduct comprehensive clinical and cognitive assessments of research participants in accordance with study protocols and standardized procedures.

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.
• Proficiency in coordination of tasks across multiple research teams.

Technical Skills & Expected Level Of Proficiency

• Budget Management - Developing
• Clinical Research Participant Recruitment: -Developing
• Clinical Study Design - Developing
• Clinical Trial Management System - Developing
• Data Management and Analysis - Developing
• Data Collection and Reporting - Developing
• Good Clinical Practices - Developing
• Interpersonal Skills - Developing
• Project Management - Developing
• Regulatory Compliance - Developing
• Report Writing - Developing

The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs.

Classified Title: Sr. Clinical Research Coordinator

Role/Level/Range: ACRP/03/MB

Starting Salary Range: $42,330 - $74,110 Annually ($51,000 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: M-F 9am - 5pm

FLSA Status: Exempt

Location: Johns Hopkins Bayview

Department name: SOM Psy Bay BV Geriatric and Neuropsychi

Personnel area: School of Medicine