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EUC Specialist (SC Cleared) - Outside IR35 - Home-based

We are currently partnering with a client who are in the market for an EUC Specialist with expertise around Windows 10 build/deployment, SCCM, InTune, Defender, End Point, and Office 365 to join the team on an initial 6-month contract to deliver several high impact projects across the organisation.

Please see a summary of the requirement below:

Role: EUC Specialist (SC Cleared)
Contract Length: 6 months

IR35 Status: Outside
Location: home-based
Start Date: ASAP
Rate: £DOE

Skills:

  • Windows 10
  • O365
  • SCCM
  • Defender ATP
  • End-Point
  • AzureAD
  • Active SC Clearance

Interviews will be taking place this week so, if you are interested, please apply today and we will be in touch as soon as possible.

Alternatively, you can reach out to Ben McKay directly and he will be in touch as soon as possible.

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Azure Engineer (SC Cleared) - Azure DC Migration - Outside IR35 - Home-based

We are currently partnering with a client who are in the market for an Azure Engineer with expertise around Windows Server, MS Azure, application re-platforming, and ideally Terraform to join the team on an initial 6-month contract to deliver several high impact projects across the organisation.

You will work on the deployment a new and migration of existing DC based applications and split them between new data centres and Azure Tenant.

Please see a summary of the requirement below:

Role: Azure Engineer (SC Cleared)
Contract Length: 6 months
IR35 Status: Outside
Location: home-based
Start Date: ASAP
Rate: £DOE

Skills:

  • Azure
  • Data centre migration
  • Windows Server
  • Experience deploying via Terraform
  • Data centre migration
  • Active SC clearance

Interviews will be taking place this week so, if you are interested, please apply today and we will be in touch as soon as possible.

Apply
*BASIC FUNCTIONS:* Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors..*SENIOR CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:* + Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study. + Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents + Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities. + Trains site staff on the EDC system and verifies site computer system. + Assists in resolving any issues in order to ensure compliance with site file audits in conjunction with ISSC. + Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports. + Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required. + Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. + May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA. + Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested. + Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items. + Assists with, and attends, Investigator Meetings for assigned studies. + Authorized to request site audits due to data integrity concerns. + Attends study-related, company, departmental, and external meetings, as required. + Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should be current at all times with the pertinent site updates/contacts. + Ensures all study deliverables are completed per IQVIA Biotech and study timelines + Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs. + Serves as mentor for junior CRAs and those new to the company and/or study. + Performs other duties, as requested..*KNOWLEDGE, SKILLS AND ABILITIES:* + Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology. + Four+ years of oncology experience and/or medical device. + Experience in monitoring and/or coordinating clinical trials required. + Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions. + Demonstrated ability to form strong functional relationships. + Excellent, presentation, organizational and interpersonal skills. + Ability to interact with all levels of staff to coordinate/execute study activities. + Ability to handle several priorities within multiple, complex trials. + Ability to reason independently and recommend specific solutions in clinical settings. + Able to mentor other CRAs and co-monitor, as required. + Understand electronic data capture including basic data processing functions. + Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research. + Able to qualify for a major credit card. + Valid driver's license; ability to rent automobile. + For the Technical CTM role, the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more..*CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:* + Ability to travel domestically and internationally + Very limited physical effort required to perform normal job duties.*MINIMUM RECRUITMENT STANDARDS:* + BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience. + Computer literacy and knowledge of electronic data capture required. + Must possess excellent verbal and written communication, interpersonal, and organizational skills. + Requires and ability to work independently, prioritize, and work within a Matrix team environment. + Prior Clinical Research Organization (CRO) experience preferred. + Prior project team leadership experience preferred. + Working knowledge of budget management preferred. + Must be able to travel domestically and internationally approximately 65%-85%. #LI-RW1 #LI-Remote At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com . IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA's Talent Acquisition team at (see below) to arrange for such an accommodation. IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
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*BASIC FUNCTIONS:* Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors..*SENIOR CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:* + Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study. + Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents + Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities. + Trains site staff on the EDC system and verifies site computer system. + Assists in resolving any issues in order to ensure compliance with site file audits in conjunction with ISSC. + Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports. + Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required. + Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. + May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA. + Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested. + Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items. + Assists with, and attends, Investigator Meetings for assigned studies. + Authorized to request site audits due to data integrity concerns. + Attends study-related, company, departmental, and external meetings, as required. + Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should be current at all times with the pertinent site updates/contacts. + Ensures all study deliverables are completed per IQVIA Biotech and study timelines + Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs. + Serves as mentor for junior CRAs and those new to the company and/or study. + Performs other duties, as requested..*KNOWLEDGE, SKILLS AND ABILITIES:* + Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology. + Four+ years of oncology experience and/or medical device. + Experience in monitoring and/or coordinating clinical trials required. + Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions. + Demonstrated ability to form strong functional relationships. + Excellent, presentation, organizational and interpersonal skills. + Ability to interact with all levels of staff to coordinate/execute study activities. + Ability to handle several priorities within multiple, complex trials. + Ability to reason independently and recommend specific solutions in clinical settings. + Able to mentor other CRAs and co-monitor, as required. + Understand electronic data capture including basic data processing functions. + Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research. + Able to qualify for a major credit card. + Valid driver's license; ability to rent automobile. + For the Technical CTM role, the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more..*CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:* + Ability to travel domestically and internationally + Very limited physical effort required to perform normal job duties.*MINIMUM RECRUITMENT STANDARDS:* + BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience. + Computer literacy and knowledge of electronic data capture required. + Must possess excellent verbal and written communication, interpersonal, and organizational skills. + Requires and ability to work independently, prioritize, and work within a Matrix team environment. + Prior Clinical Research Organization (CRO) experience preferred. + Prior project team leadership experience preferred. + Working knowledge of budget management preferred. + Must be able to travel domestically and internationally approximately 65%-85%. #LI-RW1 #LI-Remote At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com . IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA's Talent Acquisition team at (see below) to arrange for such an accommodation. IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
Apply
*BASIC FUNCTIONS:* Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors..*SENIOR CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:* + Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study. + Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents + Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities. + Trains site staff on the EDC system and verifies site computer system. + Assists in resolving any issues in order to ensure compliance with site file audits in conjunction with ISSC. + Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports. + Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required. + Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries. + May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA. + Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested. + Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items. + Assists with, and attends, Investigator Meetings for assigned studies. + Authorized to request site audits due to data integrity concerns. + Attends study-related, company, departmental, and external meetings, as required. + Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should be current at all times with the pertinent site updates/contacts. + Ensures all study deliverables are completed per IQVIA Biotech and study timelines + Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs. + Serves as mentor for junior CRAs and those new to the company and/or study. + Performs other duties, as requested..*KNOWLEDGE, SKILLS AND ABILITIES:* + Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology. + Four+ years of oncology experience and/or medical device. + Experience in monitoring and/or coordinating clinical trials required. + Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions. + Demonstrated ability to form strong functional relationships. + Excellent, presentation, organizational and interpersonal skills. + Ability to interact with all levels of staff to coordinate/execute study activities. + Ability to handle several priorities within multiple, complex trials. + Ability to reason independently and recommend specific solutions in clinical settings. + Able to mentor other CRAs and co-monitor, as required. + Understand electronic data capture including basic data processing functions. + Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research. + Able to qualify for a major credit card. + Valid driver's license; ability to rent automobile. + For the Technical CTM role, the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more..*CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:* + Ability to travel domestically and internationally + Very limited physical effort required to perform normal job duties.*MINIMUM RECRUITMENT STANDARDS:* + BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience. + Computer literacy and knowledge of electronic data capture required. + Must possess excellent verbal and written communication, interpersonal, and organizational skills. + Requires and ability to work independently, prioritize, and work within a Matrix team environment. + Prior Clinical Research Organization (CRO) experience preferred. + Prior project team leadership experience preferred. + Working knowledge of budget management preferred. + Must be able to travel domestically and internationally approximately 65%-85%. #LI-RW1 #LI-Remote At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com . IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA's Talent Acquisition team at (see below) to arrange for such an accommodation. IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
Apply
  • £500.00 - £600.00

Dynamics 365 Functional Consultant - Dynamics 365, Dynamics CE, Dynamics CRM, D365, D365 Functional Consultant, CE Consultant, Dynamics CRM Functional Consultant, Waterfall, Agile, D365, Functional Consultant - UK - Remote - £500-600pd

Our client, a growing Microsoft partner is actively looking for a number of Dynamics 365 Functional Consultants to join them on a contract basis and assist with a large-scale implementation of Dynamics 365 CE. This role will be remote for the foreseeable but in the future will require some time on-site in Central London.

Key Skills & Experience:

  • 3+ years experience as a D365 Functional Consultant
  • Previous experience working for a Microsoft Partner as a Functional Consultant is essential
  • Experience of working on 2+ full life cycle implementations of D365 CE is essential
  • Strong knowledge of D365 CE from a functional perspective
  • Full software development life cycle, in either Waterfall or Agile methodologies
  • Business analysis and best practices within the context of Microsoft Dynamics
  • Configuration of Dynamics 365 and supporting technologies
  • UI customisation (supported)
  • Business Rules and Process flows
  • Client-Side Scripting beneficial
  • Ability to build and maintain strategic relationships with Executive Level, Operational Level, IT, or business owners
  • Ability to travel and flexibility in work schedule
  • Ability to communicate with & present to all levels within a customer's business
  • Demonstrated ability to be a self-starter & independent thinker with the aptitude to work autonomously
  • Good communication skills, both verbal and written
  • Full UK driving licence

Responsibilities:

  • Documenting business needs, identify gaps between business needs and standard application functionality, design and document solutions that fill the gaps, and provide detailed business requirements specifications for developers
  • Developing and maintain business process documentation and consider compliance in all business process analysis and redesign activities
  • Performing application configuration, testing and evaluation to ensure quality and consistency
  • Developing, documenting, and executing test plans to assess the integrity and accuracy of business processes, module functionality setups and modifications, enhancements, customisations, and patches
  • Developing and maintaining end-user training documentation and deliver training as required

Location: UK Remote

Candidates must be eligible to work in this country.

Catch Resource Management is a leading provider of Dynamics 365, JD Edwards, NetSuite and other ERP resources to both end users and to product suppliers/authors.

Our consultants deliver a completely professional resourcing service, always backed up by our team of ERP specialists who are all experienced in full project life cycle implementation and support, thus ensuring that we fully understand our clients' requirements and our candidates' skills.

If you have the relevant skills and experience for this position we would welcome your application, however please note that we receive high levels of responses to our advertisements so can only immediately respond to those that are a close match. However, if you are interested in hearing about similar positions then please register on our website.

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  • £35.00 - £38.00/hour Negotiable upon experience
Senior Social Worker - MASH - Home-based - £38.00 per hour I am currently working hand-in-hand with a growing MASH Team within the Devon region as they seek to expand their team long-term to accommodate for the natural growth that is happening in 2021. As a result of this growth, they are seeking an individual to join them at a Senior Social Worker level and will provide plenty of opportunity for personal development and growth. What they can offer you: Competitive rate - Up to £38.00 hourly DOE. Consistent contract length. Home-based working (after your 1st week on the job being inducted) What they are looking for: 3 years experience working within Children's Services in MASH. Social Work England registered. If you would like to have a catch up regarding this opportunity or wish to have a confidential chat then please get in touch on (phone number removed) and ask for Liam Woods. Due to high demand this role is unlikely to remain on the market for long. Alternatively if you're not looking, you may know a colleague who might be able to benefit from knowing about these positions and I offer a referral bonus of £200 if I place your referral
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SAP Assessor 3 Month Contract Home-Based Competitive Starting Salary + Benefits Ref: SH1306 Penguin Recruitment is working alongside a specialist Sustainability Consultancy, currently looking for a Qualified SAP Assessor to join their technical team. You will be joining a growing team in a progressive company, with large projects across the area. You will be working in a home-based capacity so having the ability and confidence to work on your own initiative is ideal. This role will have a strong focus on SAP Assessments, so experience with SAP Assessments and Calculations would be ideal. Your SAP Assessor new role will also see you completing a number of tasks and duties, including: Liaise with clients to develop the Sustainability Strategy Produce SAP Calculations Being involved in SAP Assessments Consult on building design to comply with Part L Building RegulationsTo be considered for this role of SAP Assessor, you will ideally: Hole a Degree in a relevant subject/field Have experience in a similar position Be a qualified OCDEA (On-Construction Domestic Energy Assessor) Have a working knowledge of Part L Building Regulations Have a good eye for detailInterested? To discuss this position or other roles in the Sustainability Sector, please contact Sam Harris on (phone number removed), or email a copy of your CV over to and we will be in touch shortly
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Job Title: Home-based Customer Service Agent Location: Preston - CANDIDATES MUST BE ABLE TO COMMUTE TO PRESTON FOR 3 DAYS TRAINING Salary: £8.91 per hour Hours: Shift hours (40 hours per week) - We require flexibility over 7 days a week, as your shifts will be a mix of weekday and weekend hours. About Us: R2R People is a fast-growing agency with Temporary, Contract and Permanent work in the Health and Social care, Outsourcing and Legal sectors with aspirations to expand into new industries as part of a strategic plan. About the roles: We are looking to speak with anyone who is currently seeking work, as the roles we offer are varied and will suit a wide range of skillsets. The positions are in all the industries mentioned above, although we welcome applicants from all sectors, as training will be provided. The contracts will vary from 3 to 6 months, and the pay rate is £8.91 per hour. The positions we have offer shift hours (40 hours per week). Training will be delivered, which must be completed in person, usually taking around 3 days. Essential skills and experience: * Can work flexible hours * Able to work from home * Attend training sessions before the start * Able to communicate effectively Benefits: * Work from home * Training provided
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Over time, there will be opportunities to move to a permanent part-time or full-time contract with guaranteed hours if that suits you and depending on…
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