Skip to main content

This job has expired

Sr. Clinical Research Program Manager

Johns Hopkins University
Clifton East End, MD
Closing date
Apr 11, 2024

View more

Organization Type
The Division of Gastroenterology and Hepatology is seeking a Sr. Clinical Research Program Manager for the GI Clinical and Translational Research Unit (CTRU). This position will report to CTRU leadership and work in collaboration with multiple investigators in the division. The Sr. Clinical Research Program Manager will be responsible for ensuring regulatory compliance, managing the day-to-day research activities per SOP/best practices, supervising staff and working with investigators in the implementation of research studies, including multi-center trials. The Sr. Clinical Research Program Manager will also contribute to the strategic and programmatic development of the CTRU by assisting with budget planning, the effective utilization of resources, and development and implementation of Standard Operating Procedures (SOPs).
Specific Duties & Responsibilities

Project Management & Implementation
  • Assist with development of SOPs for all research related activities and staff.
  • Provide overall management of day-to-day research activities and staff.
  • Prioritize and optimize staff effort on sponsored studies by regularly assessing changing workloads based on current and anticipated active study needs.
  • Run and/or organizes internal and external meetings, collaborating among various GI groups, national research groups, national societies, non-profits, industry, and faculty members of other institutions.
  • Assist the study Principal Investigator and other co-Investigators in communications with Johns Hopkins ORA for contracting, agreements, and managing relationships with internal and external collaborators.
  • Assist PI and CTRU team with new study development, including reviewing and assessing new protocols for clarity, thoroughness, logistical feasibility, maintaining subject safety etc. If required, advise on clinical trial registration, appropriate staffing and resource needs, and coordination with research pharmacy.
  • Assist with the maintenance of a centralized listing of past, active, and future clinical research projects.
  • Manage, support, coordinate and implement study specific tasks as required including recruitment, data collection, regulatory submissions and site coordination and training for multi-center projects where JH serves as the coordinating center.
  • Develop and update/maintain study documents including protocols, amendments, case report forms, SOPs, lab manuals, training documents and regulatory materials for dissemination to study teams and satellite sites.
  • Meet with the research team at JHU and satellite sites as needed and facilitate regular communication to provide oversight and guidance in protocol implementation and adherence, recruitment methods, and to review study progress.
  • Perform other duties as assigned.

  • Develop and implement a robust quality management system to ensure compliance.
  • Manage and monitor adherence to local, state, federal entities, GCP, IRB and other applicable regulatory requirements for study team and satellite sites.
  • Provide initial and continuing training to staff and track SOM required education requirements to maintain compliance.
  • Supervise and assist staff as needed on IRB and FDA submissions to ensure compliance.
  • Assist JHU faculty and fellows with basic IRB questions and connect them with the appropriate IRB personnel.
  • Serve as the primary resource for all regulatory related matters.

  • Coordinate with ORA in budget development with sponsors.
  • In collaboration with the GI Finance team, assist with maintaining current subcontracts for subsites and development of subcontracts for new projects.
  • Facilitate meetings with the GI Finance Team and investigators to review various sponsored research accounts to ensure balanced budgets, timely invoicing and proper effort allocation of research staff.

Supervisory Responsibilities
  • Hire and supervise CTRU staff including research technologists, regulatory specialists, coordinators and nurses.
  • Orient and train new research staff on Hopkins-specific workflow to include appropriate practical shadowing and field training.
  • Provide continuing education and training including revisions/updates on regulatory policies, innovative research tools, general professional development and certifications (ACRP, SCORA) to maintain a highly skilled and dedicated research team.
  • Serve as an internal and external resource in a team environment and mentor junior research coordinator(s).

Special Knowledge, Skills, & Abilities
  • Excellent organizational skills.
  • Excellent attention to detail skills.
  • Excellent ability to manage multiple and competing priorities.
  • Excellent time management skills, with demonstrated ability for self-direction and initiation.
  • Strong oral and written communication skills, and ability to work independently.
  • Demonstrated ability to work well with other professionals with minimal supervision and be comfortable being part of a diverse professional team.

Minimum Qualifications
  • Bachelor's Degree in health-related sciences or related discipline.
  • Eight years related experience in clinical research at an academic, government, or pharmaceutical industry environment.
  • Requires minimum of two years of management experience.
  • Requires experience in clinical research and regulatory affairs.
  • Experience in protocol and informed consent writing, data analysis, grant writing, and /or manuscript preparation required.
  • Requires experience in managing or coordinating multi-site cohort studies and/or clinical trials.
  • Requires experience in clinical research and regulatory affairs including FDA regulated trials (IND/IDE).
  • Additional education may substitute for experience to the extent permitted by the JHU equivalency formula.

Preferred Qualifications
  • Certification as a Clinical Research Professional preferred.
  • Experience in budget generation, contractual process and financial management of clinical trials preferred.
  • Proficiency in writing SOPs, technical and programmatic reports.
  • Proficiency in the use of common software applications including databases (REDCap, etc.), regulatory applications (eIRB, etc.), clinical computer systems (Epic, etc.) spreadsheets, and word processing.

Classified Title: Sr. Clinical Research Program Manager
Role/Level/Range: ACRP/04/ME
Starting Salary Range: Min $64,000 - Max $112,200 Annually ($88,100 targeted; Commensurate with experience)
Employee group: Full Time
Schedule: M-F 8:30-5p
Exempt Status: Exempt
Location: School of Medicine Campus
Department name: SOM DOM Gastroenterology
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 our employees' health, life, career and retirement. More information can be found here:

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.

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 For TTY users, call via Maryland Relay or dial 711. For more information about workplace accommodations or accessibility at Johns Hopkins University, please visit

Johns Hopkins has mandated COVID-19 and influenza vaccines, as applicable. The COVID-19 vaccine does not apply to positions located in the State of Florida. 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 and all other JHU applicants should visit

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.

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert