Classified Title: Research Program Assistant II Working Title: Research Program Assistant II Role/Level/Range: ACRO40/E/02/CC Starting Salary Range: $14.00-$19.25 Employee group: Casual Schedule: Working Monday-Friday; average 10 hours per week Exempt Status: Non-Exempt Location: 04-MD:School of Medicine Campus Department name: 10002817-SOM DOM Pulmonary Personnel area: School of Medicine
Will be involved in data collection, entry and management functions in clinical research
Specific Duties & Responsibilities:
Oversee data collection, data entry, management and calculations using computerized database, word processing and spreadsheet software; review data input for accuracy and completeness.
Able to effectively prioritize and work on multiple tasks with concurrent deadlines and demonstrate excellent time management skills and efficiency
Oversee administration of standardized surveys to research subjects or their proxies via phone, or via in-patient, clinic or home visits
Assist in preparation of data reports for IRB, funding agencies, and other research sponsors.
Screening medical records to determine patient's eligibility for the study and contacting the medical team for permission
Maintain logs of patient screening, and data collection
Maintain filing system for electronic and paper-based records
Maintain compliance with IRB regulations and guidelines
Actively communicate and update faculty on patient data collection and entry status via verbal and written communication
Have initiative in anticipating and responding to staff and research subjects' needs based on awareness of routine and repeated job functions
Maintain high level of motivation for job functions with positive attitude
Attend group meetings and investigator's meetings as necessary
Communicate with study sponsors, coordinators and collaborators
Proactively seek to improve or optimize work flow and discuss with principal and co-investigators as appropriate
Conduct processes involved in study subject enrollment, including obtain informed consent from eligible patients and proxies.
Composing study procedure manuals
Escort patients through hospital during their research visit
Prepare study documents for IRB submission, including maintaining regulatory binders
Maintains quality assurance of study procedures and blinding throughout the study
Follow all written and unwritten study practices, procedures and protocols.
Organize and file participant records; prepare and maintain study materials
Schedules and coordinates study related procedures on a timely basis
Demonstrates and serves as a role model for a positive work environment, including high motivation, positive attitude, and good judgment, tact, and sensitivity in all interpersonal interactions with all research staff, investigators, students and participants
Minimum Qualifications (Mandatory):
High school diploma/GED required. 2 year related experience.
Some college courses.
Special Knowledge, Skills, and Abilities:
Strong verbal communication skills.
Experience with computer software programs.
Ability to work independently and manage multiple tasks.
Highly attentive to detail and deadlines.
Technical Qualifications or Specialized Certifications:
All IRB-required courses and appropriate study related certifications/training must be completed
The successful candidate(s) for this position will be subject to a pre-employment background check.
If you are interested in applying for employment with The Johns Hopkins University and require special assistance or accommodation during any part of the pre-employment process, please contact the HR Business Services Office at email@example.com. For TTY users, call via Maryland Relay or dial 711.
The following additional provisions may apply depending on which campus you will work. Your recruiter will advise accordingly.
During the Influenza ("the flu") season, as a condition of employment, The Johns Hopkins Institutions require all employees who provide ongoing services to patients or work in patient care or clinical care areas to have an annual influenza vaccination or possess an approved medical or religious exception. Failure to meet this requirement may result in termination of employment.
The pre-employment physical for positions in clinical areas, laboratories, working with research subjects, or involving community contact requires documentation of immune status against Rubella (German measles), Rubeola (Measles), Mumps, Varicella (chickenpox), Hepatitis B and documentation of having received the Tdap (Tetanus, diphtheria, pertussis) vaccination. This may include documentation of having two (2) MMR vaccines; two (2) Varicella vaccines; or antibody status to these diseases from laboratory testing. Blood tests for immunities to these diseases are ordinarily included in the pre-employment physical exam except for those employees who provide results of blood tests or immunization documentation from their own health care providers. Any vaccinations required for these diseases will be given at no cost in our Occupational Health office.
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