Sr. Clinical Research Coordinator (Oncology) - #Staff

Johns Hopkins University

Washington (District of Columbia)

Hybrid

USD 41,000 - 72,000

Full time

14 days+
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Job summary

Johns Hopkins University in Washington, DC is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities of a complex study or multiple trials, ensuring operational feasibility and alignment with protocol goals.

The role supports budgeting, communications, data systems, and regulatory submissions, collaborating with principal investigators and sponsors. Candidates should have a Bachelor's degree with at least three years of related experience, and be prepared to work in a

Qualifications

  • Bachelor's degree in a related field.
  • Three years of related experience.
  • Additional education may substitute for required experience per the JHU equivalency formula.

Responsibilities

  • Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design.
  • Develop standard operating procedures and data collection forms from protocol(s).
  • Develop consent form(s) for clinical trials based on protocol(s).
  • Prepare materials for submission to IRB.
  • Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services.
  • Ensure compliance with all protocols, procedures, and applicable regulations.
  • Participate in developing the study budget.
  • Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies.
  • Set up a data collection system and ensure the validity of study data.
  • Organize and quality control study data
  • Perform self-audits and/or audit other sites.
  • Participate in study meetings and provide status updates and recommend changes to protocol operations based on results and goals.
  • Conduct literature searches to provide background information.
  • Abstract and index information based on knowledge of subject matter.
  • Other duties as assigned.

Skills

Three years of related experience

Education

Bachelor's Degree in a related field
JHU equivalency formula substitutions

Job description

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a Sr. Clinical Research Coordinator who will oversee the day-to-day activities of a single complex study (e.g., in-patient study, translational research involving clinics and labs, participant accrual at multiple sites, study for which Hopkins is a coordinating center) or multiple clinical research studies and makes independent decisions that impact the conduct of the research. Assists in goal setting and creating implementation plans. Contributes to budget formulation, communications, and data systems.

Specific Duties & Responsibilities
  • Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design.

  • Develop standard operating procedures and data collection forms from protocol(s).

  • Develop consent form(s) for clinical trials based on protocol(s).

  • Prepare materials for submission to IRB.

  • Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services.

  • Ensure compliance with all protocols, procedures, and applicable regulations.

  • Participate in developing the study budget.

  • Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies.

  • Set up a data collection system and ensure the validity of study data.

  • Organize and quality control study data

  • Perform self-audits and/or audit other sites.

  • Participate in study meetings and provide status updates and recommend changes to protocol operations based on results and goals.

  • Conduct literature searches to provide background information.

  • Abstract and index information based on knowledge of subject matter.

  • Other duties as assigned.

Minimum Qualifications
  • Bachelor's Degree in a related field.

  • Three years of related experience.

  • Additional education may substitute for required experience and additional related experience may substitute for required education permitted by the JHU equivalency formula.beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Classified Title: Sr. Clinical Research Coordinator

Role/Level/Range: ACRP/03/MB

Starting Salary Range: $41,300 - $72,300 HRLY (56,800 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Mon - Fri / 8:30a - 5p

FLSA Status: Exempt

Location: Hybrid/District of Columbia

Department name: SOM Onc Sibley

Personnel area: School of Medicine

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.

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