We are seeking a Research Program Supervisor. This position requires a highly motivated, detail-oriented and proactive individual to supervise research staff at the Behavioral Pharmacology Research Unit (BPRU) and assist with the overall functioning of research projects and the study team members. The Research Program Supervisor will be accountable for staff and resource management and must have exceptional time management and organizational skills.
Specific Duties & Responsibilities:
Supervise Research Coordinators and Assistants
Complete 120-day evaluations and Annual Performance Reviews
Recruit, interview and hire research staff, submit and monitor requisitions for new hires, conduct reference checks
Prepare documents and space for new employees (e.g. phone lines, email, office space, keys)
Provide initial and ongoing training to staff including updating and maintaining RA orientation and training
Recommend and provide trainings to staff on procedures, ensure trainings are up-to-date, and develop trainings to address the changing landscape of research
Advocate and provide support and guidance to the research staff, serve as mediator in disagreements, and recommend solutions
Plan and support employees in career development opportunities, design events and promote opportunities for personal growth and development
Document performance issues and serve as the liaison to human resources for the disciplinary process
Monitor workload and recommend changes in staffing efforts and delegate appropriately, coordinate with the office manager to ensure staff have salary support and rotate staff as needed
Notify investigators of RA performance (includes areas where improvement is needed)
Routinely implement and edit policies and procedures, new hire orientation materials, and job descriptions to improve clarity and workflow
Run monthly RA and RPC meetings - prepare agenda and address group concerns, invite faculty members to present research and career story
Attend trainings, classes, and events to promote the BPRU and grow personally and professionally. Share information, techniques, and tools with staff as applicable.
Fulfill and document all parking voucher requests. Replenish parking voucher supply as needed.
Submit and follow-up on BPRU maintenance requests
Plan and coordinate staff engagement events – CPDD Week, informational sessions, employee appreciation initiatives
Student Internship Program – attend weekly meetings, create and revise policies and procedures, interview and conduct orientations with new students, complete routine check-in meetings with students to monitor performance and program satisfaction
Coordinate with Clinical Engineering to ensure completion of annual PM checks on BPRU medical equipment
Organize and purge office spaces to maximize space, safety, and efficiency
Assist Technical Supervisor with clean-up and recycling of dated equipment
Serve as a BPRU point of contact for special projects and events (e.g. building renovations)
Supervise the conduct of studies to guarantee the normal development of the research activities (recruitment, enrollment, follow-ups), reporting weekly progress to fulfill study goals in a timely manner
Coordinate participant visits and follow up, schedule appointments with study participants, track and locate participants alongside with recruitment and telephone pre-screening as necessary
Monitor staff in regard to their adherence to protocols for the recruitment of participants and delivery of study procedures to participants
Train and supervise existing and new research assistants and/or students
Assign visits to RAs, track visit completion, inform them of upcoming scheduled clinic appointments
Ensure proper written informed consent from each study participant is obtained prior to entering the study and that the original signed and dated consent form for each participant is filed in the research record
Manage study procedures concerns and/or issues that arise during visit assessments
Troubleshoot participant difficulties with assessment completion
Provide Investigators a weekly study status report covering recruitment and retention of participants and other ongoing study issues. Make recommendations for and oversee resolutions to new/outstanding operational issues. Be knowledgeable of the protocol so that study activities are completed correctly and completely
Work with principal investigator and co-investigators to develop and implement a manual of procedures that includes recruitment tools and strategies. Create protocol specific data collection forms
Prepare site IRBs, DSMB, sponsor reports and subcontract documents
Coordinate serious adverse event reporting with the investigators to ensure prompt reporting to the IRB, DSMB, and study sponsor
Serve as the point-of-contact and liaison between multiple collaborators and disciplines, including physicians, clinic administrative staff, schools, lab facilities, and pharmacies
Schedule investigator, data management and other study specific meetings, including developing agendas, reports, and minutes
Establish and follow a protocol for tracking, quality control, and maintenance of study equipment. Place study supply orders
Upload device data to server and/or input, organize, edit, and verify accuracy of data in databases in a timely fashion. Assist the data management team with resolution of data inconsistencies and maintaining protocol statistics
Run pre-established queries and develop ad-hoc queries/reports as requested. Understand the importance/impact of data integrity regarding honest reporting of sensitive and confidential patient information
Adhere to guidelines regarding the sensitivity and confidential nature of patient information
Work independently and under the direction of the Principal Investigator to ensure successful completion of the clinical research study
Exercise good judgment, tact, and sensitivity at all times while working in a busy hospital clinic environment
Assist investigators in the Hiring/Termination process
Track that study research staff are in compliance with HR, IRB, and other regulatory trainings and certifications
Assist with oversight and maintenance of petty cash account and funds for research protocol
Minimum Qualifications (Mandatory):
Bachelor's Degree in related discipline required
Two years related experience in research required
Supervisory research preferred
Additional education may substitute for required experience and additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula*
* 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 the 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.
Special Knowledge, Skills & Abilities:
Ability to work in a team dynamic and troubleshoot programmatic issues
Excellent organizational skills
Excellent oral communication skills to deal effectively within and outside the department
Excellent written communications skills
Skilled in computer programs such as Microsoft Excel, Word, Outlook, and PowerPoint
Enthusiasm and willingness to learn about the work of the department as well to acquire new technical skills as needed
Excellent organizational skills to work effectively in an environment that requires balancing multiple assignments
Ability to interact effectively with individuals at all levels and from diverse cultures.
Able to sit in a normal seated position for extended periods
Able to reach by extending hand(s) or arm(s) in any direction
Finger dexterity required, able to manipulate objects with fingers rather than entire hand(s) or arm(s), e.g., use of computer keyboard
Communication skills using the spoken word
Ability to see within normal parameters
Ability to hear within normal range
Up to 25 casual, part-time, and full-time research staff
Classified Title: Research Program Supervisor Role/Level/Range: ACRO37.5/03/CE Starting Salary Range: $18.86 - $25.93/hr (commensurate with experience) Employee group: Full Time Schedule: Monday thru Friday / 37.5 Exempt Status: Exempt Location: Johns Hopkins Bayview Department name: SOM Psy Bay Behavioral Pharm Rserch Unit Personnel area: School of Medicine
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 Talent Acquisition Office at email@example.com. For TTY users, call via Maryland Relay or dial 711.
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.
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