Clinical Research Coordinator (Behavioral Pharmacology Research Unit) - #Staff

Johns Hopkins University; Baltimore (MD); Sur place; USD 37 000 - 65 000; Plein temps

Résumé du poste

Johns Hopkins University is seeking a Clinical Research Coordinator for the Behavioral Pharmacology Research Unit at the Johns Hopkins Bayview location. The role involves coordinating all study activities, assisting with consent, IRB submissions, recruitment, and data management under the Sr. Clinical Research Manager.

Strong regulatory and organizational skills are essential. The position supports protocol implementation, participant liaison, and collaboration with nurses, PIs, and other staff

Qualifications

• Bachelor's degree in a related field is required.
• Additional education may substitute for experience per JHU policy.

Responsabilités

• Coordinate all activities of a clinical research study to ensure adherence to protocol.
• Assist in IRB submissions and liaise with study personnel.
• Explain study background to participants and obtain informed consent where appropriate.
• Schedule participants and manage data entry and study meetings.
• Oversee budget expenditures for study operations and coordinate recruitment.

Connaissances

Attention to Detail

Oral and Written Communications

Organizational Skills

Regulatory Compliance

Project Coordination

Formation

Bachelor's Degree in a related field

Outils

Clinical Trial Management System

Description du poste

The Behavioral Pharmacology Research Unit is seeking a Clinical Research Coordinator who reports to the Sr. Clinical Research Manager. Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. The Clinical Research Coordinator administratively coordinates clinical protocol implementation, typically for a single study. Will ensure the efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues.

Specific Duties & Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Participate in clinical study start-up meeting.
• Assist research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
• Explain the study background and rationale for the research to potential and current participants.
• Contribute to the development of recruitment strategy for participants for assigned study.
• Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
• Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
• Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams.
• Serve as liaison to study participants.
• Assist with setup of the data collection system and enter and organize data.
• Assist in coordinating study meetings.
• Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
• Assist with the preparation of submissions to the Institutional Review Board (IRB).
• Liaison with IRB on administrative matters and facilitate communications with the PI.
• Conduct literature searches to provide background information.
• Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
• Oversee budget expenditures for study operations.
• Other duties as assigned.

In addition to the duties described above

• Implement protocol changes and ensure that the study team is appropriately trained.
• Prepare study materials for bi-annual quality assurance checks.
• Assist with the preparation of study reports, publications, and presentations.
• Provide backup in the event of staff absences, scheduling conflicts, and other program needs.
• Contribute to BPRU initiatives outside of study related tasks.

Minimum Qualifications

• Bachelor's Degree in a related field.
• 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

• Related undergraduate or work experience in human subject research.

Technical Qualifications & Specialized Certifications

• Technical Skills & Expected Level of Proficiency
• Attention to Detail - Awareness
• Clinical Trial Management System - Awareness
• Data Entry - AwarenessData Collection and Reporting - Awareness
• Data Management and Analysis - Awareness
• Interpersonal Skills - Awareness
• Oral and Written Communications - Awareness
• Organizational Skills - Awareness
• Project Coordination - Awareness
• Regulatory Compliance - Awareness

Classified Title: Clinical Research Coordinator

Role/Level/Range: ACRO37.5/03/CD

Starting Salary Range: $17.65 - $31.05 HRLY ($41,500 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Monday thru Friday/ 8:30am - 5:00pm

FLSA Status: Non-Exempt

Location: Johns Hopkins Bayview

Department name: SOM Psy Bay Behavioral Pharm Rserch Unit

Personnel area: School of Medicine

Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.