The Clinical Research Coordinator participates in or leads day to day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Research Coordinator will develop a progressive functional knowledge of

Oversee and conduct recruitment, screening and enrolling of eligible patients into laboratory protocols. Explain the protocol in detail and conduct informed consent procedures with potential research participants. Maintain good working knowledge of all assigned protocols and reporting requirements. Maintain regulatory binders/spreadsheets for assigned protocols. Prepare a

Harkcon, Inc. is seeking to add an experienced Administrative Assistant to our National Security and Intelligence team, supporting a key customer within the Department of Energy (DOE) / National Nuclear Security Administration (NNSA). The Administrative Assistant will provide high level administrative and managerial support to upper management within DOE/NNSA. This positi

Interpret EFI job tickets and work requests and select appropriate binding and distribution techniques according to job specifications and equipment. Set up, adjust, and operate various bindery and distribution equipment (e.g., paper cutters and trimmers, folders, creasers, collators, laminators, stitchers, drills, multiple station inserters, multiple head labelers, tabbe

The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regu

The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regu

The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regu

Research Coordinator II Clinical Trials Job Locations US MD Bethesda Program Research Management Office ID 2024 4215 Category Clinical Research Position Type Regular Full Time Travel Up to 5% of the time Work Arrangements Hybrid work environment Overview Join the HJF Team! HJF is seeking a Research Coordinator II to write, edit, document, and package protocols, consent fo

Responsible for assisting with protocols from sponsors (federal and non federal) and completing actions for the protocol to receive final IRB Approval. Screens patients for eligibility, determine commitment, and obtain informed consent. Educates patients about the research study, their roles and other vital information. Adheres to legal, professional, and ethical codes wi

Leads a variety of unit, department, or division level research initiatives. Provides direction to study teams regarding protocol development and study conduct. Directs and prepares for study monitoring visits or audits. Responds to and formulates corrective action plans for audit/monitor findings. Demonstrates day to day accountability and provides direct administration

The Clinical Research Coordinator participates in or leads day to day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Research Coordinator will develop a progressive functional knowledge of

The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regu

Manage all aspects of clinical trials related to investigational products, including training of pharmacy staff, maintenance of IP binders and drug accountability records, maintenance of IP blinding and unblinding processes, attendance at site initiation visits and feasibility committee meetings, and review of protocols and investigational brochures Ensure stability condi

The Department of Neurology is seeking a part time (24 hours/week) Sr. Research Program Coordinator who will be responsible for coordinating clinical trials and other clinical research projects in the Johns Hopkins Multiple Sclerosis Center. This will involve, but is not limited to, screening medical records, identifying appropriate patients, consenting study participants

Participate in the development, implementation, testing, and evaluation of manuals, questionnaires, and coding structures, for the efficient collection of data. Participate as a member of a collaborative group in study design and analysis of data. Adhere to all protocol requirements to ensure validity of clinical research data. Participate in and oversee data collection.