Clinical Data Specialist Jobs
By Intellectt Inc At Alameda, CA, United States
At Least 3 years of experience in clinical data management and computer savvy. Some project management skills are needed.
Clinical data management experience needed.
They must be open to do menial tasks if they have 5 years experience.
Hybrid role (4 days onsite and 1 day remote)
A team player and flexible; quick and eager to enter into ADC.
Product: a sensor that will b put on the patient
Data Scientist, Rwe Clinical Trials, Remote
By Walgreens At Deerfield, IL, United States
Bachelor's degree or graduate degree and at least 4 years of experience in a quantitative or computational function
4 years of experience in R, Python, or SQL.
Experience in designing and executing robust and reproducible statistical analyses in the context of epidemiology and observational research with healthcare data
Experience processing large data from various data sources
Experience handling protected patient health information
Knowledge of at least one of the following: Tableau, Power Bi, Alteryx, Spotfire, or other BI intelligence tools
Clinical Research Data Entry Specialist I/Ii - Remote
By Frederick National Laboratory for Cancer Research At United States
Provides data entry and management support to an assigned caseload of research protocols
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
Reviews study protocols and assists in the planning and implementation of the data management aspects of clinical research projects
Possession of a Bachelor's degree from an accredited college/university, or qualifying experience in lieu of required education
Cloud–based clinical data management systems (e.g., Medidata Rave) and enrollment tracking systems (e.g., OPEN)
Works collaboratively with VRS team members, site staff, and data monitors to meet program and protocol requirements, deadlines, and deliverables
Research Data Assistant - Clinical Trials (Full Time, Day Shift)
By Nicklaus Children's Hospital At , Miami, 33155
High School education or equivalent
Assists study staff with any concerns or questions by promptly providing the information and feedback as requested
Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.
Provides auditable trail of documentation with consistency among data base, records and required reports
Provides reports on grant progress and assists in troubleshooting
Serves as liaison for Research Institute with all departments involved with the study.
Travel & Trials Event Specialist
By Kirkland & Ellis At Los Angeles, CA, United States
Manage and effectively communicate Firm’s travel needs to vendors/resources.
Work on developing internal processes to enhance travel experience for attorneys and staff.
A minimum of 5 years of experience in travel or hotel sales and a Bachelor’s Degree.
Establishment and promotion of strong working relationships with external contacts and suppliers to ensure the Firm’s needs are understood and met.
Creation and dissemination of travel resource communication to the Firm.
Develop relationships with paralegals to assist with their trial related travel needs including contracting hotel guest room and meeting space.
Clinical Trials Data Specialist
By Stanford University School of Medicine At Stanford, CA, United States
Knowledge, Skills And Abilities (required)
Experience with Electronic Data Capture (EDC)
Some knowledge of medical terminology
Strong clerical, interpersonal, and organizational skills.
Ability to exercise judgment and employ basic reasoning skills.
Extraction and entry of required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).
Clinical Data Specialist Jobs
By Merative At United States
Pharmacy technician certification plus 2 years related work experience, or 4 years related work experience.
Demonstrated ability to effectively communicate with management and other team members
Demonstrated ability to apply pharmacy knowledge and experience in critical thinking and problem solving; ability to recognize discrepancies in data
Perform data normalization prior to data entry, using controlled terminology and following strict editorial guidelines
Strong computer skills; familiarity with Microsoft Office products (e.g., Word, Excel, Access) and Adobe Professional
Solid knowledge of internet searching and pharmaceutical terminology
Clinical Trials Data Coordinator - Remote
By City of Hope At California, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Clinical Trials Data Coordinator - Remote
By City of Hope At Duarte, CA, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Clinical Trials Specialist Jobs
By Axle Informatics At Bethesda, MD, United States
Stay abreast of project management certification standards and industry principles through professional associations and implements practices. 4
Creates project in designated project management software and ensure all necessary staff have access.
Recommend and support routine project management meetings, updates and prepare a variety of status reports and dashboards.
Assist staff coordinate project management activities, to include routine meetings and development of reports.
Conducts project analysis and reports to upper management.
Develop summaries of project status and performance for review with upper management.
Clin Trials Rsrch Asst/Data Mg
By University of Iowa At Iowa City, IA, United States
Protocol Development/Management And Study Responsibilities
Provide general assistance, as needed, to the PIC clinic and administrative managers, faculty and staff.
Excellent Written And Verbal Communication Skills Are Required.
Assist in the conduct of sponsored clinical trials, including the collection of clinical data and the compilation of results.
Assist in the design and development of data collection forms, questionnaires, and procedures manuals.
Design forms to facilitate the collection and tracking of study participant data, study drugs, biological specimens and study procedures.
Clinical Trials Specialist (Multiple Vacancies)
By Rutgers University At New Brunswick, NJ, United States
Equivalent education, experience and/or training may be substituted for the educational requirement.
Minimum of three (3) years of clinical research experience.
At least one (1) year of oncology experience.
Bilingual skills (English/Spanish); speaking, reading, and writing.
Collaborates with Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list.
Serves as an essential link between patients and all other members of the research team.
Clinical Trials Data Entry Specialist
By UCLA Health At , Los Angeles, 90095, Ca $24.28 - $48.04 an hour

Description As the Data Entry Specialist, you will participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica while under the direction of the ...