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Clinical Research Data Specialist Jobs

100%Remote Role || Clinical Research Specialist
By Cloud Space LLC At United States
Skills & Experience (top 3 skills):
•Quality Management System/Regulatory Compliance Program
Location:100% remote – EST support Henry Ford in Detroit (Remote)
Work Experience (do not edit):
•Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Insert major accountabilities in chart
Clinical Research Specialist, (Hybrid, Irvine)- Tmtt
By Edwards Lifesciences At Irvine, CA, United States
Experience in site monitoring/central monitoring skills, site qualification, and site training
Data management experience or analytics
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Remote Clinical Research Specialist
By Comrise At California, United States
REMOTE Clinical Research Specialist ( Medical Device)- 6 months contract- May go perm
o Preferred, experience with electronic file system, Medidata and Sharepoint & Smartsheet.
5 + years, BA required. o Working as CRA (clinical research associate.)
o Familiar GDP (good documentation practices)
o Filling clinical trial documents ETMF
Clinical Research Specialist Jobs
By Roth Staffing At United States
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Must have knowledge in reference to good clinical practices regulations and standard operating procedures.
The job requires the ability to make judgements based on practice and previous experience.
Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.
Clinical Research, Imaging Specialist
By University of Chicago At Chicago, IL, United States
Manages the analysis of complex imaging data.
Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
Motor Vehicle Record Inquiry Required
Clinical Data Management Specialist
By TalentBurst, an Inc 5000 company At Irvine, CA, United States
Proven track record or validating, testing, and meeting reoccurring deadlines regarding data management.
Position: Analyst, Clinical Data Management
2-4 years of experience required.
Experience with EDC (Electronic Data Capture) systems required.
Good computer skills in Microsoft Office Suite
Good written and verbal communication skills and interpersonal relationship skills
Clinical Research Data Analyst
By LHH At New York City Metropolitan Area, United States
Administration and management of EDCs, including creation of eCRFs, study configuration, and UAT
Creation and interpretation of study management reports
Familiarity with Electronic Data Capture systems and data management
Solid skills in data entry, monitoring /QA and data analysis/statistics
Manage user accounts and provide support to sites
Minimum 3years’ experience in a related healthcare position
Clinical Research Protocol Specialist
By Frederick National Laboratory At ,
Previous study coordination and/or project management experience in clinical research
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
Knowledge of regulatory requirements and guidelines for facilitating clinical human subjects research, including Health and Human Services (HHS) regulations
Serves as the point-of-contact and project manager for an assigned portfolio of projects
This position is located in Rockville, Maryland. Remote work is possible.
Strong collaborative skills with ability to build relationships within multiple groups
Clinical Research Data Specialist I - Cedars-Sinai Center For Outcomes Research And Education (Cs-Core) - Part-Time
By CEDARS-SINAI At , Los Angeles, Ca $23.39 - $39.76 an hour
Participates in required training and education programs.
Experience in a similar position is highly preferred.
Maintains the accuracy, integrity and security of complex, large computerized records systems.
Understands regulations, policies, protocols, and procedures to control and maintain accurate records.
Performs data searches and other related administrative tasks.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Clinical Research Specialist I
By Cedars-Sinai At Los Angeles, CA, United States
May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
Participates in required training and education programs.
Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution.
Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
Coordinates research projects at an institutional or departmental level.
Communicates project status and improvement areas with leadership in a timely manner.
Transportation Data Specialist (Research Assistant 1)
By University of Connecticut At , Storrs, 06269, Ct $50,000 - $55,000 a year
Coordinate with data stewards on data development, asset digitization, and Linear Referencing system (LRS) integration requirements for physical asset data collection.
Excellent oral and written communication skills.
Basic knowledge of maps and spatial data.
Bachelor’s degree; civil engineering, transportation, or other related disciplines that are deemed appropriate and relevant to this position may be considered.
Ability to establish and maintain cooperative relations with superiors, associates, and additional data stakeholders, including municipal representatives and the general public.
Attention to detail, particularly related to enforcing data validation rules and quality assurance/quality control procedures.
Research Data Specialist ($25/Hour)
By WCG At Puyallup, WA, United States
Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement
Advanced knowledge of Microsoft Word, Excel, Outlook, Databases and Adobe Acrobat
Strong writing and interpersonal skills
Knowledge and ability to utilize computers and related technology efficiently
Demonstrated team player who is self-initiated to take on different roles/responsibilities and can work well in groups
Ability to function effectively in a fast-paced environment and manage multiple projects simultaneously
Research Data Specialist ($25/Hour)
By WCG At , Puyallup, Wa $25 an hour
Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement
Advanced knowledge of Microsoft Word, Excel, Outlook, Databases and Adobe Acrobat
Strong writing and interpersonal skills
Knowledge and ability to utilize computers and related technology efficiently
Demonstrated team player who is self-initiated to take on different roles/responsibilities and can work well in groups
Ability to function effectively in a fast-paced environment and manage multiple projects simultaneously
Clinical Research Data Coordinator
By Boston Childrens Hospital At , Brookline, 02445, Ma
Provide data coordination and data management support for Nelson Lab research studies.
Comfortable representing data-related, data management interests in team-wide conversations
Experience providing educational support and training to research investigators and staff
Interface with the Principal Investigators, project managers and staff, and external collaborators on a routine basis.
Excellent computer skills, including expertise in Microsoft Office software (e.g., Excel), R and/or Python, SPSS, and familiarity with SAS and STATA
Experience in formatting and exporting data for statistical analyses
Clinical Research Data Scientist
By SGS Consulting At United States

Location: Bay Area, CA(100% Remote) Approved Meta Remote Locations: Denver, CO, New York, NY, Houston, TX, Los Angeles, CA, and San Diego, CA. Clinical Research Data Scientist, Health ...

Clinical Research Contract Specialist (Paralegal Preferred)
By M3 USA At Raleigh, NC, United States
2+ years of experience of administrative, contract management or paralegal experience is required.
Collaborate with Finance and key operational team members to incorporate project status into projections.
CRO or site network experience
Prior experience work with clinical research site budgets.
Prior Paralegal or negotiation of contract language experience.
Basic knowledge of medical terminology and a working knowledge of drug development services desired.
Clinical Research Specialist Jobs
By croxconsulting At Naples, FL, United States
Knowledge and Skill Requirements/Specialized Courses and/or Training:
·Manage Investigator-Initiated clinical research studies.
·Lead required cross-functional research meetings to discuss studies and get input from product managers.
·Manage data collection compliance via tracked milestones.
·Responsible for the execution of clinical projects while adhering to budget, scope and schedule requirements.
•4 years of relevant clinical research experience required
Clinical Research Specialist Jobs
By Beacon Hill Staffing Group At Chicago, IL, United States
§ Create the protocol schedule of events/calendar within the Clinical Trial Management system.
§ Transcribe existing negotiated budgets into the Clinical Trial Management system.
§ Cross-reference the budget with the contract, payment terms, coverage analysis and informed consent to ensure consistency.
§ Set up financial and operational data of clinical studies in the CTMS
§ Other miscellaneous duties as needed.
Research Data Coordinator 1 - Clinical Research Management Office – Lombardi Comprehensive Cancer Center - Georgetown University Medical Center
By Georgetown University At , Washington, 20007, Dc
Ensures accuracy of data entered in the Clinical Trials Management System (CTMS) with patient information and key dates
Clinical Research Management Office (CRMO) members: Clinical Research Nurses, Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators, Laboratory Technicians
Ensures query resolution with proper physician and clinical study team oversight within site- and sponsor-specific time requirements
Assures ongoing compliance with all departmental, institutional, and federal requirements and regulations
Works in compliance with Human Subject Protection regulations, patient confidentiality/HIPAA requirements, and Good Clinical Practice
Up to 2 years of related experience
Research Data Specialist ($25/Hour)
By WCG At Cary, NC, United States
Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement
Advanced knowledge of Microsoft Word, Excel, Outlook, Databases and Adobe Acrobat
Strong writing and interpersonal skills
Knowledge and ability to utilize computers and related technology efficiently
Demonstrated team player who is self-initiated to take on different roles/responsibilities and can work well in groups
Ability to function effectively in a fast-paced environment and manage multiple projects simultaneously