Career Center
Port Orchard, Washington
Port Orchard, Washington
Port Orchard, Washington
Bethlehem, Pennsylvania
California
South San Francisco, California
Posted: 05-Jan-23
Location: Baltimore, Maryland
Salary: Open
Internal Number: 107244-en_US
We are seeking a Research Program Coordinator who will be responsible for coordinating clinical research activities within the Johns Hopkins Myositis Center. Requisite tasks will include patient recruitment and scheduling, data collection and management, specimen handling, compliance with IRB regulations, and administration myositis research projects. The individual will act as a liaison between the principal investigator, School of Medicine, Research Administration, GCRC, funding agencies and other study related organizations.
Specific Duties & Responsibilities
Clinical Research Activities
- Assist the principal investigator with myositis clinical research projects.
- Identify potential study participants and assist in their recruitment into other research studies.
- Assist clinicians with patient screening and verification of eligibility for specific research studies.
- Obtain informed consent from potential study participants after providing a detailed description of the study, the study procedures, and potential risks, and answering all questions.
- Schedule patients appointments and follow-up visits/phone calls at the appropriate time to assure completion of protocol requirements. This may require coordination of multiple appointments and centers.
- Perform structured tests in the clinic and complete various assessment tools and questionnaires related to each study.
- Collect patient source documents and case report forms for analyzing patient data.
- Be responsible for the organization, entry, maintenance and accuracy of patient clinical research data.
- Coordinate same-day blood shipments for cohort studies to central lab for processing.
- Act as primary contact for study participants, which may include scheduling, confirming appointments, and escorting/directing to various locations on campus
- Establish study calendar of various clinical protocols and coordinate the logistics needed for successful completion of the studies.
- Maintain detailed working knowledge of all assigned protocols. Adhere to all protocol requirements to ensure the validity of clinical research subject data
Regulatory Compliance
- Comply fully with institutional and external clinical research requisites.
- Responsible for Institutional Review Board (IRB) submission, verification and maintenance of protocol specific information. Prepare and submit annual renewal requests, amendments, and safety reports according to IRB requirements.
- Design and compile materials which aid physicians and other staff in complying with protocol requirements
- Maintain regulatory binders per protocols
- Document and report adverse events and protocol deviations.
- Organize and create clinical research charts to be reviewed by regulatory agencies.
- Complete training requirements for biohazard material handling and department of transportation (DOT) shipping requirements.
- Be familiar with good clinical practice guidelines and knowledge of sponsor and FDA guidelines.
Data Management
- Maintain and promptly update online Clinical Research Management System for each study protocol.
- Assist with preparation of data for reports and presentations.
- Respond in a timely manner to special projects or queries related to data.
- Design and implement procedural adjustments to increase accuracy and efficiency of data collection and entry process.
- Perform quality checks on data entry.
- Ensure accuracy and timeliness of data collection. Interact regularly and facilitate the completion of work with members of the research team regarding data management and the status and progress of ongoing studies.
- Abstract patient clinical and demographic from a variety of sources and enter into tracking spreadsheet or data base.
Scholarly Activities
- Assist with writing manuscripts and abstracts for publication.
- Assist with development of grants, progress reports and study protocols.
Research Program Oversight
- Meet regularly with Principal Investigators to review data accuracy and overall study progress.
- Work with Center manager and study sponsor (where appropriate) on problem recognition/resolution, accuracy of data gathered and patient well-being, completion and collection of regulatory documents required by sponsors.
- Prepare for and participate in audits of studies including follow-up item.
Financial Management
- Keep records of expenditures and work with budget analysts to ensure accurate and prompt reporting of study financials
- Maintain compensation records for participants.
General
- Carry out duties and responsibilities with limited supervision.
- Travel to and participate in investigator and research coordinator meetings.
- Maintain equipment and order research supplies related to clinical research protocols.
- Report progress to Center Director and ensure satisfactory completion of research projects.
Minimum Qualifications
- Bachelor's Degree in related discipline.
- Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula.
Classified Title: Research Program Coordinator
Role/Level/Range: ACRO40/E/03/CD
Starting Salary Range: $16.75-$23.00-$29.30 HRLY (Commensurate with experience)
Employee group: Full Time
Schedule: M-F 8:30am - 5Pm
Exempt Status: Non-Exempt
Location: Hybrid/School of Medicine Campus
Department name: SOM DOM Bay Rheumatology
Personnel area: School of Medicine
Total Rewards
The referenced salary range is based on Johns Hopkins University's good faith belief at the time of posting. Actual compensation may vary based on factors such as geographic location, work experience, market conditions, education/training and skill level. Johns Hopkins offers a total rewards package that supports the health, life, career and retirement. More information can be found here: https://hr.jhu.edu/benefits-worklife/
Please refer to the job description above to see which forms of equivalency are permitted for this position. If permitted, equivalencies will follow these guidelines:
JHU Equivalency Formula: 30 undergraduate degree credits (semester hours) or 18 graduate degree credits may substitute for one year of experience. Additional related experience may substitute for required education on the same basis. For jobs where equivalency is permitted, up to two years of non-related college course work may be applied towards the total minimum education/experience required for the respective job.
**Applicants who do not meet the posted requirements but are completing their final academic semester/quarter will be considered eligible for employment and may be asked to provide additional information confirming their academic completion date.
The successful candidate(s) for this position will be subject to a pre-employment background check. Johns Hopkins is committed to hiring individuals with a justice-involved background, consistent with applicable policies and current practice. A prior criminal history does not automatically preclude candidates from employment at Johns Hopkins University. In accordance with applicable law, the university will review, on an individual basis, the date of a candidate's conviction, the nature of the conviction and how the conviction relates to an essential job-related qualification or function.
The Johns Hopkins University values diversity, equity and inclusion and advances these through our key strategic framework, the JHU Roadmap on Diversity and Inclusion.
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.
EEO is the Law
Learn more:
https://www.eeoc.gov/sites/default/files/migrated_files/employers/poster_screen_reader_optimized.pdf
Accommodation Information
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 Talent Acquisition Office at jhurecruitment@jhu.edu. For TTY users, call via Maryland Relay or dial 711. For more information about workplace accommodations or accessibility at Johns Hopkins University, please visit accessibility.jhu.edu.
Johns Hopkins has mandated COVID-19 and influenza vaccines, as applicable. Exceptions to the COVID and flu vaccine requirements may be provided to individuals for religious beliefs or medical reasons. Requests for an exception must be submitted to the JHU vaccination registry. For additional information, applicants for SOM positions should visit https://www.hopkinsmedicine.org/coronavirus/covid-19-vaccine/ and all other JHU applicants should visit https://covidinfo.jhu.edu/health-safety/covid-vaccination-information/.
The following additional provisions may apply, depending on campus. Your recruiter will advise accordingly.
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.
Note: Job Postings are updated daily and remain online until filled.
