weekend days or after hours. Assists with organization, maintenance and operations in the laboratory including ordering and receiving laboratory reagents. Assist in the preparation of grant proposals and manuscripts. Maintains both handwritten and computerized records of work performed.
Candidate is expected to assist in the generation of mouse models for hematologic malignancies and perform techniques such as oral gavage, tail-vein and intra-peritoneal injections, submandibular bleeding, and harvest and analysis of animal tissues post-sacrifice. Following training, candidate is expected to perform procedures such as injections and blood draws in mice, maintain careful records of mouse
health, procedures and euthanasia. Should be able to independently perform cell biology techniques such as flow cytometry. Data analysis and the production of oral and written reports, participation in team meetings at which the work will be discussed and planned.
Assist in drafting grant proposals and manuscripts. Assist the lab head in preparation of research proposals to external funding agencies. Ordering and receiving special items, tracking supplies and restocking will be the candidate's responsibility. Qualifications: Associate's degree required A minimum of 3-6 month relevant research experience required PDN-9ae3e1fa-308d-4cc5-91ea-0cbd4347950d
teams, recruiting study participants, obtaining parental permission/assent, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining study records, interfacing with study sponsors, participation in sponsor study monitoring visits.
Qualifications: Bachelors degree in Health related science; effectively uses Microsoft computer software; demonstrates ability to coordinate and establish priorities among diverse tasks; effectively communicates verbally and in writing At least one year relevant experience required Must have ACRP Certification or sit for the exam as soon as eligible Primary Responsibilities: Follows all aspects
of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned; Develops source documents, parental permission and assent documents for submission to IRB.
Coordinates IRB submissions for assigned studies, maintains regulatory documents during conduct of study; develops and utilizes study participant and family teaching tools for study purposes; interfaces with representatives of sponsoring agencies. Participates in the conduct of parental permission/assent process for assigned studies; schedules study visits with study participants in accordance
with study protocols; develops strategies to assure compliance of study participants with protocol requirements.
Performs clinical data gathering and measurements and monitoring of data integrity, including data completeness, accuracy and quality. Maintains study databases Participates in training nursing and ancillary study staff for study purposes; recruits, screens and enrolls sufficient number of study participants in conformance with protocol requirements. Assists in identifying, reporting and following-up on Serious Adverse Events. Assists in the maintenance of study medication accountability records; prepares clinical specimens for shipment to central laboratories.
Coordinates monitoring activities with Sponsor's representative(s). Completes Case Report Forms; responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS. PDN-9acfc2db8c-a2eb-72fe4dc2a260
