HVIVO SERVICES Salary

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7 reviews in total
  London
QUEEN MARY BIOENTERPRISES INNOVATION CENTRE 42 NEW ROAD LONDON E1 2AX
TIN: 02326557
Rating of the company
based on 0 evaluations
7 reviews in total

Earnings on positions in HVIVO SERVICES

HVIVO SERVICES is looking for employees for positions:

it apprentice

Responsibility

  • the Key Resposibilities of the role will be
  • promptly respond to enquiries, helping staff troubleshoot hardware and software issues, ensuring their problems are resolved efficiently
  • offer guidance and support to users in navigating computer equipment and software applications as needed
  • take ownership of user problems, demonstrating a proactive approach in addressing their issues, and providing clear explanations of potential solutions
  • create comprehensive follow-up actions and escalate issues to the appropriate teams within the organisation when necessary
  • delegate more intricate service issues to our skilled 2nd Line IT Engineers for resolution
  • generate and deliver supporting reports to stakeholders as requested, ensuring transparency and communication throughout the support process
  • friendly face and voice of our IT support team, serving as the first point of contact for users via face-to-face, email, or chat, offering assistance to our user base

Requirements

  • skills and experience
  • ensuring the Windows operating systems are up-to-date
  • building and maintaining laptops
  • daily checks of services and alerts
  • procurement of accessories used by IT and staff
  • IT helpdesk overview and ticket updates, escalation or closure
  • provide IT project support to the business
  • can do attitude

marketing manager

Working hours

  • permanent

Responsibility

  • including
  • develop and execute volunteer enrolment marketing plan
  • support the FluCamp contact centre with volunteer communication materials
  • management of the lead generation for FluCamp Clinical Trials Recruitment
  • management of dedicated lead generation budgets
  • management of external vendors
  • the marketing manager will be responsible for all activities relating to the development and the day-to-day execution and administration of the marketing plan
  • creation of advertising material for all different channels

Requirements

  • previous experience within a CRO or a pharmaceutical / healthcare environment would be advantageous
  • the successful candidate will be responsible for understanding our organisation, key priorities and applying a digital approach to marketing campaigns including content creation and distribution as well as logistical and operational aspects in-person and using digital aspects to enhance community engagement
  • attention to detail, ability to manage within a high demand environment, strong interpersonal communications skills, and a focus on execution and results are a must

laboratory technician

Responsibility

  • produce and maintain required documentation concerning study-specific sample receipt, processing and storage
  • perform receipt, processing , storage and transport of subject’s samples as specified by Standard Operating Procedures and GCP
  • perform molecular, cell culture and assays as required and as specified by SOPs and GCP
  • develop laboratory skills as required for assigned projects
  • maintain compliance with Good Clinical Practice, all relevant SOPs, to company standards and guidelines
  • work as part of a team, maintaining excellent communication between staff at different sites and between divisions
  • perform receipt, processing and storage of samples according to an analytical plan, within specified timeframes to GCP standards, ensuring milestones are reached
  • assist with the production of kits and labelled samples

Requirements

  • GCSE or BTEC in a Science subject
  • previous experience of working within a laboratory environment
  • good communication skills
  • to be able to work as a member of a team, responsible for organising own time and resources in an optimal fashion, with some guidance

systems administrator

Responsibility

  • implement industry best practices
  • system owner responsibilities including validation, documentation, and end user training
  • maintenance and administration of existing systems
  • on site & offsite IT and Vendor engagement as required
  • key point of contact for all ‘owned’ internal/external IT project issues
  • keeping your knowledge of systems up to date in order to support the business needs
  • interdepartmental and cross-functional work to ensure delivery of business and project targets
  • IT helpdesk support for tickets raised against supported applications

Requirements

  • essential
  • MS Windows 7/10
  • MS Office
  • validation of business systems
  • system testing
  • end user testing
  • experience automating website workflows
  • project management skills

financial accountant

Working hours

  • permanent

Responsibility

  • financial and Management Reporting
  • balance sheet reconciliations
  • supporting the preparation of VAT returns
  • supporting the timesheet submission process
  • assisting the Financial Accountant with debtor recovery
  • support with project/departmental accounting ensuring that costs are recorded in the correct place, driving the revenue recognition process
  • the role will support the Group Financial Controller and Financial Accountant with the day to day, month to month running of the operational finance department
  • assisting with audit requests

Requirements

  • required experience
  • part qualified and working towards an accounting qualification
  • experience with balance sheet reconciliations
  • full understanding of debits and credits and accrual accounting
  • bonus experience
  • experience within a clinical research organisation or within the life sciences sector

clinical lead

Responsibility

  • management of the company’s computer systems validation processes
  • responsible for maintaining overall CSV compliance and supporting each systems owner in doing so for their system
  • work as part of system implementation teams for the implementation of LIMS and clinical e-source systems
  • liaise with business stakeholders to define user requirements and create user test scripts
  • perform computer system validation testing and error resolution
  • work with development teams and validation teams to refine detail and resolve issues
  • challenge business to simplify process and introduce efficiency
  • maintain CSV documentation

Requirements

  • demonstratable hands on experience in GxP computer systems validation
  • excellent written and verbal communication skills
  • strong project management skills including scope and timeline management
  • be capable of championing the adoption of systems and process and embedding their use within the organisation
  • A strong working understanding of GCP and GCLP

senior systems engineer

Working hours

  • permanent

Responsibility

  • maintain the validation status of required systems in line with GxP and in line with good system life cycle management
  • assist other departments with change controls that affect IT systems
  • provide operational and IT support to areas of the business, ensuring keen prioritisation and project documentation
  • system/SQL Server administration
  • testing and documentation of system deployment, ongoing maintenance, and retirement
  • work with external suppliers and systems to deliver to business needs
  • documentation and trending of ongoing system technical issues

Requirements

  • MS Windows
  • MS Windows Server
  • MS Office
  • windows Active Directory
  • group Policies
  • MS Exchange
  • MS SQL Server
  • linux

internal auditor

Working hours

  • permanent

Responsibility

  • identify and assess Quality Management System non-compliances and ensure appropriate actions are agreed and effectively followed up
  • support with CAPA investigations, and/or conduct CAPA investigations under supervision
  • support QA team with eQMS SOP activities as required
  • become familiar with and maintain an up-to-date knowledge of the current legislation
  • ensure compliance of the quality management system documentation
  • under supervision, plan, conduct and follow up internal process, system, facility, study and document audits and external supplier audits in line with the audit programme to verify compliance
  • support with QA training delivery and organisation
  • work cross functionally to follow up and close out audits including review/agreement of appropriateness of corrective actions to audit findings with relevant hVIVO staff

Requirements

  • GCP or GCP for laboratories experience
  • knowledge of drug development processes
  • working knowledge of GCP and GCP for laboratories regulatory standards
  • excellent attention to detail
  • degree in Science or equivalent
  • knowledge of GLP and GMP standards and Quality Assurance auditing experience would also be desireable

marketing executive

Working hours

  • permanent

Requirements

  • the successful candidate will be responsible for understanding our organisation, key priorities and driving a digital approach to marketing campaigns including content creation and distribution
  • attention to detail, ability to manage within a high demand environment, strong interpersonal communications skills, and a focus on execution and results are a must

Responsibility

  • ensuring all events are communicated effectively to the wider team
  • manage spend under the direction of the Marketing Manager

recruitment administrator

Working hours

  • permanent

Responsibility

  • the main responsibilities for the role are as follows
  • responsible for production and distribution of routine operational reports within the agreed schedule
  • ensure departmental databases are updated and maintained at the agreed frequency
  • ensure the timely delivery of external client and vendor reports within the agreed schedule
  • assist with ad-hoc data requests as necessary
  • provide support with minute taking and maintaining action logs
  • provide assistance in study funnel maintenance
  • provide QC of databases and support stakeholders with the identification and resolution of data quality issues within their respective areas

Requirements

  • if you have the following skills and experience we would like to hear from you
  • demonstrated experience in reporting and data in a commercial environment
  • understanding of good data recording practices; ability to spot data anomalies and escalate as appropriate
  • comfortable with sharing and presenting data/reports and dealing with queries for a wide range of business stakeholders
  • experience in a clinical research environment desireable
  • if you feel you would like to be