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Job Req ID:  103821

Sr. Compliance Monitoring Specialist

The Center for Psychedelic and Consciousness Research is seeking a Sr. Compliance Monitoring Specialist who will take the lead on compliance monitoring and regulatory management of several clinical trials involving the administration of psychoactive substances to both healthy and patient populations. The Sr. Compliance Monitoring Specialist will ensure the quality, accuracy, and integrity of clinical trial data and regulatory documents throughout the full lifecycle of multiple clinical trials.


Specific Duties & Responsibilities

  • Manage study progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
  • Participate in risk assessments by reviewing studies for quality assurance and general content.
  • Develop standard and protocol-specific forms, trial-specific monitoring plans, and SOPs.
  • Ensure the collection and maintenance of required essential documents.
  • Assist in training new research staff regarding research compliance and regulatory documents.
  • Generate monitoring summary reports and communicate these findings to Investigators and Research Staff.
  • Verify that written informed consent is obtained before each subject's participation in the trial.
  • Verify that source documents, other trial records, and CRFs are accurate, complete, and legible and that CRF entries reflect the source.
  • Communicate deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator and take appropriate action designed to prevent the recurrence of the detected deviations.
  • Help study staff prepare for external audits. Participate in unscheduled internal reviews and compliance monitoring reviews on an as-needed basis.
  • Educate principal investigators and/or individual coordinators regarding study procedures, regulatory requirements, and other study responsibilities.
  • Other duties as assigned.


Special Knowledge, Skills, & Abilities

  • Ability to work independently and exercise the judgment necessary.
  • Excellent written and interpersonal communication skills and the ability to build effective relationships both internally and with outside regulatory officials (e.g. DEA, FDA).
  • Knowledge of medical terminology and human subject research.
  • Strong organizational, IT, and administration skills with attention to detail.
  • The candidate must be proficient in Microsoft Excel and Word.
  • Knowledge of IRB and FDA guidelines.


Minimum Qualifications
  • BA/BS in medical research or scientific discipline, health care related, or other appropriate discipline preferred.
  • Minimum 5 years of experience with clinical trials/medical research required.




Preferred Qualifications
  • Certified Clinical Research Associate (CCRA) credentialing is preferred.
  • Experience with quality assurance or clinical trial auditing/monitoring, and/or good clinical practice preferred.

Classified Title: Sr. Compliance Monitoring Specialist  
Role/Level/Range: ACRP/04/MD  
Starting Salary Range: $54,080-$74,390 Annually (Commensurate with experience) 
Employee group: Full Time 
Schedule: Monday thru Friday 8:30 -5:00 
Exempt Status: Exempt 
Location: ​​​​​​​Johns Hopkins Bayview 
Department name: ​​​​​​​SOM Psy Bay Behavioral Pharm Rserch Unit  
Personnel area: School of Medicine 

 

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.

 

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.

 

 

Johns Hopkins Bayview