Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry.Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.Assure compliance with the protocol and regulatory requirements includes: collecting, recording...
Prepare and process all Institutional Review Board (IRB)through the IRB and other regulatory groups as apropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events.Coordinate, organize and maintain all documentation required by sponsor or CRO (c...
Manage regulatory aspects of clinical research studies (e. Assisting in the development/maintenance of study specific case report forms, source document tools, trackers, and templates to be used by research staff. ...
Assisting with writing research results and grant reports. Leading annual holiday suicide myth research project. Recruiting undergraduate student coders, training them to work on content analysis and other quantitative and qualitative research projects, and assessing inter-coder reliability using Kr...
Clinical Research Coordinator (Recruitment Only)-(16001534). The Clinical Research Coordinator, in collaboration with the Clinical Investigators at the Lewis Katz School of Medicine, will be responsible for the planning, implementation, and execution of Clinical Trials in the assigned department. Re...
Consent patients and coordinate visits, lab blood draws and tissue acquisition.Collect, process, and ship biospecimens.Abstract data from electronic medical records.Accurately and efficiently enter data into REDCap.Assist in the creation, organization, and maintenance of spreadsheets and databases.A...
The Clinical Research Coordinator B will have the responsibilities described above working with minimal staff supervision; and, be responsible for collaborating with faculty in special research projects. The clinical research coordinator A (CRC A) will be responsible for data entry, organizing, main...
The enterprisersquo;s Consumer Market Research team conducts primary research to support strategic marketing and advertising decisions within these business units as well as for the entire enterprise. Responsibilities:Assist with a full portfolio of quantitative and qualitative studies into consumer...
The Clinical Research Coordinator collects, prepares and distributes information necessary for protocol development and study initiation at the Rothman Institute Orthopaedics. He or she maintains integrity & quality of research data, patient enrollment process, data analysis for various medical publ...
Clinical Research Coordinator Pool-(24001701). ...
The management team works closely with internal and external stakeholders on key projects that are foundational to the organization’s publication of high-quality science regarding the latest cancer research advances that inform the scientific and clinical research communities served by the AACR. The...
PT Clinical Research Coordinator-Opthalmology-(24001523). ...
As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. ...
Clinical Research Coordinator in Media, PA (19063). Bachelor's Degree; 1+ Years of Clinical Research Coordinating experience. ...
Under the direction of the Principal Investigator(s), Co-Investigators, and Research Manager, the clinical research coordinator will be given various research duties for multiple research and quality improvement projects. The Clinical Research Coordinator I will be aiding the Research Team and Princ...
Clinical Research Coordinator A. Clinical Research Coordinator A. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. Responsible for study coordination for investigator-initiated stu...
Under moderate supervision from study PI or other research study management staff, this role provides substantial coordination level support for all clinical research activities within the scope of clinical research protocols. Support the safety of clinical research patients/research participants. C...
As a Research Coordinator, you will be responsible for coordinating all aspects of Mid Atlantic Retina's phase 1 through phase 4 clinical research trials. College degree in related health science or 2 years Clinical Research work experience. Cross-covers for other Coordinators as needed. ...
Demonstrated experience with research and project coordination on social and/or behavioral science research studies in public health. Under supervision of the Principal Investigator (PI) and working in close cooperation with other study investigators, personnel, and students, this fulltime Study Coo...
The research coordinator will work predominately on a multicenter study evaluating the efficacy of a positive parenting intervention (PriCARE) and on a multicenter child abuse pediatrics research network (CAPNET). Under minimal supervision, the coordinator will facilitate all clinical research activ...
Experience with qualitative or mixed methods research, clinical trials, and/or community-based participatory research. This role supports research projects focused on mental health prevention for Black men and boys, and other traditionally excluded populations. You will play a key role in coordinati...
Upper School Science Research Program Coordinator (P/T). Germantown Friends School is seeking a part-time coordinator for its recently created Upper School Science Research program. This half-time position involves teaching science research sections that meet twice over an 8-day cycle, supporting st...
We have an opportunity for a full-time Clinical Research Coordinator to join our Research team. The Clinical Resarch Coordinator is a research professional who ensures oversight and compliance of both system-wide and local clinical research activities. Overall, the Clinical Research Coordinator is t...
Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. CCRC - Cert Clin Research Coordinator (Preferred). Coordinates and facilitates the conduct of ...
Clinical Research Coordinator A. Follow study protocols and S0Ps to recruit potential research participants, study eligibility, obtain informed consent, administer study assessments, and conduct research interviews for employees as needed. The University of Pennsylvania, the largest private employer...