Clinical Research Supervisor (Neurology)

Johns Hopkins University•Baltimore, MD

2d•$20 - $35•Onsite

About The Position

The Department of Neurology is seeking a Clinical Research Supervisor to oversee the Peripheral Nerve Clinical Research Program. This role involves administratively coordinating the implementation of clinical protocols for one or multiple studies. A key responsibility will be the supervision of at least two full-time research team members who will carry out protocol-related operational tasks. Researchers at Johns Hopkins University are dedicated to conducting clinical trials and studies to discover new methods for preventing and treating diseases and other health issues.

Requirements

Bachelor's Degree in a related field.
Two 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

Lead or supervisory experience.
Participation and timely completion of JHU supervisory classes

Responsibilities

Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
Facilitate administrative hiring processes and participate in staff interviews and hiring decisions.
Delegate and oversee performance of study tasks.
Set performance goals, coach staff, and conduct performance evaluations.
Participate in clinical study start-up meeting.
Assist research nurses, principal investigators, and other study personnel in executing protocol-related activities.
Understand and explain the study background and rationale for the research to potential and current participants and/or assigned research staff.
Contribute to the recruitment strategy for participants for assigned study.
Implement a variety of techniques for recruitment as needed, e.g. print and web-based advertisements, contact referring physicians, participate in community events, etc. and involve and oversee staff.
Independently conduct the consenting process or ensure consent is obtained on appropriate participants by trained staff.
Contact, or oversee contact of, participants to schedule for required activities and with special instructions prior to upcoming tests/exams.
Assist with, or oversee the setup of, the data collection system and entry and organization of data.
Assist in coordinating study meetings.
Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
Assist with the preparation of submissions to the Institutional Review Board (IRB).
Liaison with the IRB on administrative matters and facilitate communications with PI.
Conduct literature searches to provide background information.
Obtain and maintain excellent operating knowledge of assigned clinical protocols, clinical equipment, and clinical computer systems.
Oversee budget expenditures for study operations.
Other duties as assigned.