Sr. Clinical Research Coordinator II (Infectious Disease)

Johns Hopkins University•Baltimore, MD

10d•$49,200 - $86,200•Hybrid

About The Position

The Division of Infectious Disease is seeking a Sr. Clinical Research Coordinator II who will provide administrative, regulatory, and operational support for the portfolio that includes the Rakai Community Cohort Study (RCCS), IN-STEP clinical trial, the SENTINEL study, and multiple ancillary and investigator-initiated studies focused on HIV, sexually transmitted infections, non-communicable diseases, and related population health research.

Requirements

Bachelor's Degree in a related field.
Five years of related experience.
Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Nice To Haves

Master's Degree in a related field.

Responsibilities

Collaborate with PI and study team 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 studies based on protocol(s).
Prepare materials for submission to IRB and follow-up on regulatory issues.
Train and provide oversight of research data management and regulatory issues.
Work with commercial and/or government agency sponsors to recommend and/or determine what group can commit to considering patient population, available resources, and cost of providing services.
Work with the finance team to develop study budget(s) and ensure that all study costs are included in the budget.
Ensure clinical research protocol has a completed Prospective Reimbursement Analysis (PRA), and processes/systems are in place to ensure the PRA is followed when required.
Ensure adequate system for tracking and reporting clinical research milestones for financial invoicing.
Initiate and/or maintain activities, systems and processes to increase referrals and increase accruals to clinical trials.
Participate in development, testing and evaluation of manuals, questionnaires, and coding structures, for the efficient collection of data.
Organize and quality control study data.
Oversee data collection at a single site or at multiple sites of a multi-centered clinical trial.
Perform self-audits and/or audit other sites.
Participate in study meetings to present data, provide status updates, recommend changes to protocol operations based on results and goals, and suggest ideas for sub-studies.
Extract data, review literature, and assist with preparation of manuscripts and presentations as appropriate.
May oversee day-to-day activities and provide training for study staff.
Other duties as assigned.
Coordinate day-to-day administrative and operational activities for RCCS, IN-STEP, SENTINEL, and other CCGHE-ID/RHSP-related research studies.
Maintain regulatory files and track approvals, expirations, and required submissions across Johns Hopkins, RHSP, and collaborating institutions.
Serve as a central point of contact for investigators, RHSP staff, laboratories, and collaborators to support communication and follow-up.