The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure ac...
Minimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ experience preparing for and fully supporting monitoring/auditing visits preferred. Additional experie...
The ACC seeks a full-time NCI/NCTN Senior Regulatory Affairs Study Start-Up Specialist to participate in the coordination of Phase I-III clinical trials sponsored by the NCI/NCTN. The NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory ...
The ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. The ACC OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Pha...
The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...
The CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the data accurate, complete and verifiable from source documents. The Clinical Research Quality Speciali...
The ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. The ACC OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Pha...
Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. ...
SOP(Standard Operating Procedure).SDV: Source Data Verification).IRB (Institutional Review Board)....
The Consumer Finance Institute (CFI) seeks a well-trained and motivated senior research assistant to support the research of its staff and visiting scholars. Previous Senior Research Assistants have gone on to top graduate schools in economics and business. The Federal Reserve Bank of Philadelphia i...
Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in cli...
Pharmaceutical Research Associates, Inc. ...
The Senior Research Associate (SRA) leads, trains, and mentors a highly collaborative, interdisciplinary research and evaluation team and provides deep knowledge in specific subject areas. Trains, develops, and mentors employees' research and project skills, knowledge, and abilities; supervises proj...
The RA III manages Research Assistants and Research Associates working on research and evaluation tasks including sampling, weighting, data management, statistical analysis, continuous quality improvement, reports and presentation. The Research Associate III (RA III) functions in a highly collaborat...
Research, Part Time, Biology, Assistant, Department, Technology, Education. ...
The Public Health Project Coordinator is responsible for one or more public health projects for NNCC. The portfolio of projects may be subject to change as projects evolve and/or new funding opportunities arise. The Coordinator work closely with the FAIR Project Manager and the Director of Nurse Adv...
Clinical Research Coordinator A. Promote good clinical practice in the conduct of clinical investigations, including possessing and in depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate the day-to-day managem...
Clinical Research Assistant A will perform research and administrative tasks for research projects and clinical trials within the Penn Infectious Diseases Clinical Trials Unit (ID CTU). Involvement in trials will range from several weeks to serving as the primary research assistant for a study handl...
We are looking for someone who has strong project management experience with PennDOT Highway Occupancy Permit and municipal land development projects in Southeastern PA. ...
Clinical Research Coordinator A: Coordinate and implement research projects focused on lung transplantation. Clinical Research Coordinator B: In addition to the above, the CRC-B will establish workflows, pathways, and methods to operationalize protocols, regularly prepare, draft, and submit regulato...
Weissinger is seeking a Research Assistant (RA) to work on multiple research projects. Work as a research assistant on a prior community-engaged research project related to behavioral health. Posting Details (Default Section) Posting Number: 20240581T Position Title: Research Assistant Position Type...
Performs a variety of research, data base and clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data. Works under direct supervision and assists research coordinators with organizing, gathering and compiling clinical resear...
Assist with the planning and execution of clinical research projects. Perform other duties as assigned by the clinical research supervisor or manager. Prior experience in clinical research or a healthcare setting is highly desirable. Strong understanding of research methodology and clinical trial de...
This position requires an experienced Research Coordinator to assist in clinical research tasks related to Cardiology. This person will be responsible to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient oriented clinical an...
Project Manager - OSP Construction Fiber Construction experience for a Direct-Hire role in the Harrisburg, PA area (Central Pennsylvania or South central, PA). Project Manager you will be responsible for ensuring the deployment of fiber primarily in Central Pennsylvania or South-central PA area. Pro...