№ files_lp_4_process_3_099097
File format: docx
Character count: 9344
File size: 56 KB
Year:
Not specified
Location:
Morley, UK
Department:
Trading Standards
Position Level:
WY09
Reporting To:
Safeguarding and Investigations Manager
Work Style:
Office-based with fieldwork
Legislation Framework:
Proceeds of Crime Act 2002, Police and Criminal Evidence Act 1984, Regulation of Investigatory Powers Act 2000, Human Rights Act 1998, Theft Acts 1968 & 1978, Anti-Terrorism Crime and Security Act 2001, Criminal Procedures and Investigations Act 1996, Data Protection Act 1998, Fraud Act 2006, Serious Crime Act 2015, Criminal Justice Act 1988
Qualifications:
Degree level or equivalent, Accredited Financial Investigator (Part 2 & 8 powers)
Experience:
Criminal and financial investigations, money laundering investigations, working under pressure, court procedures
Skills:
Numerical and analytical skills, report writing, communication, collaboration with law enforcement and legal teams
Responsibilities:
Financial investigations, confiscation of criminal assets, liaison with law enforcement and legal authorities, preparing court applications, producing statements and evidence, maintaining stakeholder communication, managing restraint orders
Price: 8 / 10 USD
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Year:
Jubilee Year
Region / City:
Morley, WA
Topic:
Pilgrimage, Christian Hope, Religious Reflection
Document Type:
Religious Retreat Reflection
Organization / Institution:
Infant Jesus Church
Author:
Scott Cowdell
Target Audience:
Catholics, Christians, Pilgrims
Period of Validity:
Jubilee Year
Date of Approval:
Not specified
Date of Changes:
Not specified
Year:
2023
Organization:
Morley Newlands Academy
Position:
Level 1 Teaching Assistant
Application Deadline:
22 September 2023, 9am
Location:
Morley, Leeds, UK
Type of Document:
Employment Application Form
Author:
Applicant (confidential)
Target Audience:
Job applicants for teaching assistant role
Legal References:
Rehabilitation of Offenders Act 1974, Exceptions Order 1975 (2013 & 2020)
Data Privacy:
The GORSE Academies Trust Privacy Notice
Year:
2026
Location:
Morley College London – Waterloo
Position Type:
Part-time (0.8 FTE)
Salary:
£31,044 - £34,620.80 pro-rata incl. LWA
Grade:
AOC 35 - 39
Responsible to:
Head of School of Humanities and Applied Sciences
Responsible for:
Lecturers (Sessional, Lecturers, Senior Lecturers), other staff/volunteers in the programme area
Working Hours:
28.8 hpw including some evenings and occasional weekends
Annual Leave:
38 days per annum excluding public holidays and closure days
Main Activities:
Operational management, curriculum development, quality assurance, student advising, staff management, contribution to teaching
Target Audience:
Students and potential students in Health and Science courses
Reporting Requirements:
Self-Assessment Report (SAR), Annual Quality Review (AQR), Quality Enhancement Plans (QEPs)
Endorsing Bodies:
Ofsted, QAA, Awarding Bodies, Office for Students (OfS)
Type of Document:
Job description / institutional record
Grade:
8
Subject:
English Language Arts
Type of document:
Educational worksheet
Author:
Morley Callaghan (story), St. Paul’s Intermediate (worksheet)
Audience:
Students
Assignment type:
Reading comprehension and analysis
Content:
Short story analysis, multiple choice, short answer, and visual representation
Date assigned:
Not specified
School:
St. Paul’s Intermediate
Year:
2012
Location:
San Diego, California, USA
Topic:
Sports and Rehabilitation
Document Type:
News Article
Organization:
The San Diego Union-Tribune
Author:
Logan Jenkins
Event Date:
April 22–23, 2012
Related Event:
First national wounded warriors tennis camp, May 16–19, 2012
Sponsoring Organizations:
Balboa Tennis Club, San Diego District Tennis Association, U.S. Olympic Committee, ThanksUSA
Audience:
General public
Date of meeting:
7 November 2024
Location:
Morley, West Yorkshire, England
Organization:
Morley Town Council
Committee:
Community Support Committee
Document type:
Meeting minutes
Chair:
Cllr Kimberley Brown
Deputy Chair:
Cllr Edwards
Attendees:
Cllr Bullock, Cllr Hill, Cllr Dalton
Council officers present:
Town Clerk, Deputy Town Clerk
Public attendance:
8 members of the public
Apologies for absence:
Cllr Langstaff
Agenda topics:
Community grants, emergency bleed kits, CCTV servicing, community events, expenditure approvals
Grant recipients:
Morley Bridge Street FC; Morley Allstars; Legends of Morley
Approved grant amounts:
£500; £1,250; £500
Public safety initiatives:
Emergency bleed kit provision in Morley town centre
Legal references:
Public Health Act 1936 Section 234; Local Government and Rating Act 1997 Section 31
Financial decisions:
Creation of cost code and budget for life-saving equipment; transfer of £2,000 from policing budget; approval of CCTV servicing cost £330; approval of £385 invoice for event promotional materials
Community events discussed:
Yorkshire Day; Lantern Festival; Christmas Lights Switch On
Next meeting date:
9 January 2025
Year:
2026
Location:
Morley, West Yorkshire, UK
Department:
Trading Standards
Job Grade:
WY09
Reporting to:
Trading Standards Team Manager (WY11)
Employment Type:
Hybrid
Key Responsibilities:
Business development, regulatory compliance support, Primary Authority, ADR, training, partnership development
Qualifications:
Degree level or equivalent; relevant legal or regulatory qualification
Experience:
Delivering target-based outputs, legislative advice, project management, stakeholder engagement, training delivery
Skills:
Knowledge of civil law, Primary Authority regime, business advisory, report preparation, IT proficiency, communication, teamwork, problem-solving
Certifications:
Trading Standards Practitioner status (desirable)
Year:
20____
Region / City:
Randall County, Texas
Topic:
Legal Procedure
Document Type:
Motion
Organ / Institution:
Randall County District Court
Author:
[Attorney for Defendant]
Target Audience:
Legal Professionals, Court Officials
Period of Effectiveness:
From the date of approval
Date of Approval:
[DATE OF CASE ASSIGNMENT]
Date of Changes:
None indicated
Context:
This is a legal document requesting the appointment of a private investigator to assist a defendant in preparing a defense in a criminal case.
Note:
Year
Subject:
Clinical Trials, Medical Research
Document Type:
Template
Organization / Institution:
EU Clinical Trials Expert Group
Target Audience:
Sponsors of clinical trials
Note:
Year
Document type:
Checklist
Target audience:
Investigators, IRB staff
Context description:
A checklist for investigators and IRB staff to assess and ensure regulatory compliance in clinical and non-clinical research studies.
Year:
2025
Region / City:
Doha, Qatar
Topic:
Human Research Protection
Document Type:
Manual
Institution:
Virginia Commonwealth University
Author:
Huron Consulting Group
Target Audience:
Researchers, Investigators, Staff
Approval Date:
08/07/2025
Modification Date:
Not specified
Period of validity:
Not specified
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Year:
2025
Institution:
Yale University; Yale New Haven Health System
Document type:
Administrative request form
Subject area:
Human subjects research oversight
Regulatory framework:
U.S. federal human research protection regulations
Responsible body:
Institutional Review Board
Related system:
IRES IRB
Intended users:
Principal Investigators; Unaffiliated Investigators
Scope:
Authorization and oversight of unaffiliated investigators
Jurisdiction:
United States
Ethical standards referenced:
Belmont Report; HHS 45 CFR 46; FDA 21 CFR 50; HIPAA
Approval authority:
Yale/YNHHS Institutional Signatory Official
Note:
Year
Document Type:
Clinical Research Delegation Log
Author:
Principal Investigator / Investigator of Record
Target Audience:
Research Staff
Document type:
Agreement
Institution:
Oregon State University
Program:
Human Research Protection Program
Oversight body:
Institutional Review Board
Research area:
Human subjects research
Parties:
Individual Investigator; Oregon State University
Compliance framework:
International, federal, state, and local laws and regulations
Training requirements:
Research ethics training; CITI or equivalent
Approval requirement:
Institutional Review Board review and approval
Signature fields:
Investigator; HRPP Administrator
Year:
1989
Region / City:
Australia
Theme:
Clinical trials, therapeutic goods, medical research
Document Type:
Operational procedures
Organization / Institution:
SESLHD
Author:
SESLHD
Target Audience:
Coordinating Principal Investigators, Sponsors, Clinical Trial Coordinators
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Year
Document type:
Template
Institution / organization:
EU Clinical Trials Expert Group
Target audience:
Sponsors of clinical trials
Year:
2020
Region / City:
Tampa, Florida
Topic:
Human Subjects Research
Document Type:
Manual
Institution:
University of South Florida (USF)
Author:
USF Institutional Review Board
Target Audience:
Researchers and Investigators
Period of validity:
Ongoing from September 22, 2020
Approval Date:
September 22, 2020
Modification Date:
Not specified
Context:
A manual outlining procedures, regulations, and policies for conducting human subjects research at the University of South Florida, including requirements for IRB review and oversight.
Year:
Not specified
Region / City:
Maricopa County
Subject:
Law Enforcement, Criminal Investigations
Document Type:
Job Description
Agency:
Maricopa County Sheriff’s Office, Public Defender’s Office
Author:
Not specified
Target Audience:
Individuals seeking employment as investigators
Period of validity:
Not specified
Approval Date:
Not specified
Date of amendments:
Not specified