Sr. Clinical Research Coordinator (Oncology)

Johns Hopkins University; Baltimore (MD); Hybrid; USD 41,300 - 72,300; Full time

Job summary

Johns Hopkins University is seeking a Sr. Clinical Research Coordinator to oversee day-to-day activities in clinical trials. You will develop study protocols, manage data collection, and ensure compliance with regulations.

The role requires a Bachelor’s degree and three years of related experience. This full-time position offers a starting salary range of $41,300 - $72,300 HRLY, commensurate with experience.

Qualifications

• Bachelor's Degree in a related field.
• Three years of related experience in clinical research.
• Experience in developing standard operating procedures.

Responsibilities

• Oversee day-to-day activities of clinical studies.
• Develop consent forms and materials for IRB submissions.
• Set up and ensure validity of data collection systems.
• Conduct literature searches and abstract information.

Skills

Operational feasibility assessment

Regulatory compliance

Data management

Budget development

Education

Bachelor's Degree in a related field

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