CrawlJobs Logo
Kisaco Research Logo Kisaco Research · Media

Senior Conference Producer, Life Sciences

United Kingdom · Job Posted March 19, 2026
Apply Position
Job Link Share

Job Description

We are seeking a highly motivated and experienced conference producer to join our fast-growing event series in Life Sciences. The successful candidate will be responsible for managing and executing the production of industry leading events across the US, ensuring that they drive engagement and deliver exceptional value to our attendees.

Job Responsibility

  • Undertake research and analysis to determine the commercial viability of conferences within the portfolio, scaling existing products and launching new events
  • Collaborate with industry experts and thought leaders to develop engaging agendas
  • Develop ideas for creative digital content to support commercial campaign
  • Identify and recruit high-profile speakers and moderators
  • Work with the marketing lead to identify appropriate marketing channels and to ensure that the correct market segments are reached
  • Collaborate with the marketing team to develop and implement effective promotion strategies
  • Identify potential sponsors and work with the Commercial Partnerships Manager to agree on the sales plan for your event campaign
  • Work with speakers, consultants, journalists, and other information providers to source and repurpose materials for content marketing
  • Build the identity and create buzz around each event with the marketer in the build-up to and during a conference through social media including LinkedIn
  • Develop and manage budgets for each conference, ensuring financial goals are met
  • Work closely with cross functional teams to ensure seamless execution
  • Manage onsite delivery of the event being sure to gain feedback from all those attending
  • Actively participate in designing and delivering training for the production team and assume a mentor role for junior producers

Requirements

  • Graduated/graduating with a 2:1 or above
  • Minimum of 1-2 years’ experience in B2B Events
  • Analytical, commercially minded and dynamic
  • Ability to articulate and present complex information in an engaging and simple way
  • Great communication skills both written and verbal
  • English Fluency
  • Right to work in the UK
  • Ability to write crisp engaging copy for a technical/scientific audiences
  • Highly organised, methodical, and process-driven
  • High level of attention to detail

What we offer

  • £100 personal development budget
  • £200 personal wellness budget
  • Hybrid working (3 days in office, 2 from home)
  • Access to the best Tech – including Gong and Sales Navigator
  • 25 days of annual leave (in addition to bank holidays)
  • An additional day off for your birthday each year
  • 1 extra day of annual leave per year up to 30 days total
  • Regular social and charitable events
  • Annual Summer & Christmas parties
Kisaco Research - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Senior Conference Producer, Life Sciences

8 matching positions

Executive Director, HEOR Modeling

As part of Parexel Consulting, you will play a vital role in helping biopharmace...
Location
Location
United Kingdom
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Numerous years’ experience in the life sciences or consulting industries with many years of experience managing direct reports, directing teams and projects
  • 10+ years management experience
  • 15+ years general experience in the field
  • Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline
Job Responsibility
Job Responsibility
  • Monitors profitability of multiple projects through active involvement in the preparation of project plans and management of project budgets
  • Prevents and resolves issues with revenue recognition
  • Works within a team environment or individually based on project needs
  • Provides guidance to project team members and acts as a mentor to junior staff
  • Works within broad project guidelines and leads issue and conflict resolution
  • Prioritizes own workload and prioritizes the workload of the project team in order to achieve the project scope and objectives
  • Capitalizes on opportunities to improve project efficiency, results or team performance and proactively acts
  • Leverages information from previous projects or other client work to efficiently complete assigned project activities as well as facilitate business decisions
  • Produces quality work that meets the expectations of Parexel HEOR Consulting and the client
  • Reviews the work of colleagues for content and quality to ensure the expectations of the client and are met
Read More
Arrow Right

Senior Associate - RWE Obesity Statistical Programming

Amgen is seeking a dedicated Senior Statistical Programmer to join our Center fo...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
  • At least four (4) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
  • Experience in SQL, and statistical programming using SAS or R
Job Responsibility
Job Responsibility
  • Write, test and validate software programs in Unix and Databricks to produce analysis datasets and presentation output such as tables and figures, to be included in reports for submission to regulatory agencies, publications and other communications
  • Provide technical solutions to programming problems within CfOR
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming function and participate in multidisciplinary project team meetings
  • Manage all programming activities, according to agreed resource and timeline plans
  • Ensure all programming activities on the project adhere to departmental standards
  • Write and/or review and approve all programming plans
  • Write and/or review and approve analysis dataset specifications
  • Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc.
  • Write, test, validate and execute department-, product- and protocol-level macros and utilities
Read More
Arrow Right

Biostatistical Programming Senior Manager

In this vital role you will be responsible for developing and leading teams in t...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 2 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
  • Master’s degree and 8 to 10 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
  • Bachelor’s degree and 10 to 14 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
  • Diploma and 14 to 18 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
  • At least eight (8) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
  • Managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources in a statistical programming team working with real-world healthcare data (RWD)
  • Experience leading a statistical programming team within RWE
  • RWE generation in pharmaceutical or related research industries, or statistical programming for clinical trials
  • Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model
  • Department or multi-team management
Job Responsibility
Job Responsibility
  • Provide technical solutions to programming problems within the Centre for Observational Research (CfOR)
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming function and participate in multidisciplinary project team meetings
  • Project manage programming activities, according to agreed resource and timeline plans
  • Ensure programming activities adhere to departmental standards and SOPs
  • Write and/or review and approve programming plans
  • Write and/or review and approve analysis dataset specifications
  • Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc.
  • Write, test and validate software programs in Unix to produce analysis datasets and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications
  • Write, test, validate and execute department-, product- and protocol-level macros and utilities
What we offer
What we offer
  • Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Read More
Arrow Right

Senior Associate Biostatistical Programming

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Ta...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Business Analytics, or related field OR
  • Bachelor’s degree and 2 years of directly related experience OR
  • Associate’s degree and/or 4 years of directly related experience OR
  • High school diploma / GED and 6 years of directly related experience
  • At least four (4) years of relevant statistical programming experience in a clinical development or life sciences setting, including postgraduate research experience
  • Experience in SQL, and statistical programming using SAS and R
  • Track record establishing analysis standards, QC/QA processes, and controlled change management.
  • Experience or willingness to learn the process of delivering regulatory-grade analyses and submission-ready deliverables
  • Foundational understanding of medical statistics (e.g., study design, hypothesis testing, confidence intervals).
  • Real-world evidence (RWE) generation in pharmaceutical or related research industries, or statistical programming for clinical trials
Job Responsibility
Job Responsibility
  • Develop, test, validate, and execute programming code and macros that generate analysis datasets and tables, listings, and figures to support decision making in drug development
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming team and collaborate with peers in clinical and epidemiology functions
  • Manage programming activities and provide technical solutions to programming issues
  • Ensure programming activities adhere to departmental standards and SOPs as well as local compliance and regulatory standards
  • Write and review programming plans and dataset specifications
  • Review key study-related documents including but not limited to statistical analysis plans (SAPs) and data management plans (DMPs)
  • Participate in the development of departmental policies and controlled documents
  • Participate in the recruitment of programming staff
  • Actively participate in external professional organizations, conferences, and meetings
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
  • Fulltime
Read More
Arrow Right

Senior Associate Biostatistical Programming

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Ta...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Business Analytics, or related field OR Bachelor’s degree and 2 years of directly related experience OR Associate’s degree and/or 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience
  • At least four (4) years of relevant statistical programming experience in a clinical development or life sciences setting, including postgraduate research experience
  • Experience in SQL, and statistical programming using SAS and R
  • Track record establishing analysis standards, QC/QA processes, and controlled change management
  • Experience or willingness to learn the process of delivering regulatory-grade analyses and submission-ready deliverables
  • Foundational understanding of medical statistics (e.g., study design, hypothesis testing, confidence intervals)
  • Real-world evidence (RWE) generation in pharmaceutical or related research industries, or statistical programming for clinical trials
  • Strong individual contributor, proficient in developing analysis datasets, identifying data anomalies, and ensuring program accuracy
  • Motivated to learn how to work with real-world healthcare data (RWD) such as MDV and DeSC
  • Experience with Git-based version control and maintaining analysis documentation
Job Responsibility
Job Responsibility
  • Develop, test, validate, and execute programming code and macros that generate analysis datasets and tables, listings, and figures to support decision making in drug development
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming team and collaborate with peers in clinical and epidemiology functions
  • Manage programming activities and provide technical solutions to programming issues
  • Ensure programming activities adhere to departmental standards and SOPs as well as local compliance and regulatory standards
  • Write and review programming plans and dataset specifications
  • Review key study-related documents including but not limited to statistical analysis plans (SAPs) and data management plans (DMPs)
  • Participate in the development of departmental policies and controlled documents
  • Participate in the recruitment of programming staff
  • Actively participate in external professional organizations, conferences, and meetings
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Read More
Arrow Right

Senior Associate Biostatistical Programming

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Ta...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Business Analytics, or related field OR Bachelor’s degree and 2 years of directly related experience OR Associate’s degree and/or 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience
  • At least four (4) years of relevant statistical programming experience in a clinical development or life sciences setting, including postgraduate research experience
  • Experience in SQL, and statistical programming using SAS and R
  • Track record establishing analysis standards, QC/QA processes, and controlled change management
  • Experience or willingness to learn the process of delivering regulatory-grade analyses and submission-ready deliverables
  • Foundational understanding of medical statistics (e.g., study design, hypothesis testing, confidence intervals)
  • Real-world evidence (RWE) generation in pharmaceutical or related research industries, or statistical programming for clinical trials
  • Strong individual contributor, proficient in developing analysis datasets, identifying data anomalies, and ensuring program accuracy
  • Motivated to learn how to work with real-world healthcare data (RWD) such as MDV and DeSC
  • Experience with Git-based version control and maintaining analysis documentation
Job Responsibility
Job Responsibility
  • Develop, test, validate, and execute programming code and macros that generate analysis datasets and tables, listings, and figures to support decision making in drug development
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming team and collaborate with peers in clinical and epidemiology functions
  • Manage programming activities and provide technical solutions to programming issues
  • Ensure programming activities adhere to departmental standards and SOPs as well as local compliance and regulatory standards
  • Write and review programming plans and dataset specifications
  • Review key study-related documents including but not limited to statistical analysis plans (SAPs) and data management plans (DMPs)
  • Participate in the development of departmental policies and controlled documents
  • Participate in the recruitment of programming staff
  • Actively participate in external professional organizations, conferences, and meetings
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
  • Fulltime
Read More
Arrow Right

Senior Medical Writer - FSP

As a Medical Writer at Parexel, your strong scientific knowledge, writing skills...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
  • Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP
  • Extensive clinical/scientific writing skills
  • Scientific background essential
  • writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar
  • Advanced word processing skills, including MS Office (expertise in Word)
  • software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel)
  • Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation
  • Excellent interpersonal, verbal, and written communication skills
  • Ability to consistently produce documents of high quality
Job Responsibility
Job Responsibility
  • Author Clinical Documents: Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy
  • Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input
  • Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions and other processes, as applicable
  • Perform literature searches/reviews as necessary to obtain background information and training for development of documents
  • Review statistical analysis plans and mock statistical output to determine appropriateness of content/format for clinical writing
  • Quality Control: Ensure that all work is complete and of high quality prior to team distribution or shipment to client
  • Confirm data consistency and integrity across the document
  • Prepare documents for publishing readiness, when applicable
  • Ensure document structure, content, and style adheres to FDA/EMA or other appropriate regulatory guidelines, and comply with departmental, corporate or client SOPs and style guidelines, as applicable
  • Provide suggested alternative content when contributors provide content that does not meet document needs
What we offer
What we offer
  • Foster a culture of inclusivity, collaboration, and support
  • Continuous learning from being mentored to job shadowing, job rotation, and stretch assignments, as well as becoming a mentor or leading a team
  • Development and promotion based on global standards and your personal development plan
  • Supportive and inclusive environment
  • Career growth and development
  • Mentorship
  • Flexible work
  • Diverse projects
  • Culture of excellence
  • Global exposure
Read More
Arrow Right

Tax Assurance & Risk Management Assistant Manager / Manager

Our tax professionals draw on their comprehensive experience to deliver business...
Location
Location
United Kingdom , Greater Manchester
Salary
Salary:
Not provided
bdo.co.uk Logo
BDO UK LLP
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Can act as a key point of contact within the firm for the client, together with senior members of the team
  • Experience of TA&RM work (including such as tax process, tax strategy, SAO, CCO, tax risk registers etc) – with a keen interest in tax governance and developing tax operations
  • Broad tax technical experience to be able to talk knowledgeably at a good level about a range of tax issues
  • Experience in end-to-end project delivery and quality advice / report writing skills
  • Strong presentation style, and confidence in hosting workshops, training sessions and webinars, often to Board level
  • Educated to degree level, and/or CTA and/or ACA qualified or equivalent, or relevant experience
Job Responsibility
Job Responsibility
  • Excellent client relationship, communication and project management skills with the ability to distil tax concepts into easily understood information suitable for a wide array of stakeholders
  • Most of your work will be client facing, reporting to senior managers, directors and partners, and will require you to actively manage your client portfolio and manage project delivery, coordinating teams to deliver exceptional client service, in addition to supporting business development activities
  • This role will involve consideration of a range of taxes including corporate, indirect and employment taxes
  • act as a key point of contact within the firm for the client, together with senior members of the team
What we offer
What we offer
  • Health and wellness programmes
  • Pension plan
  • Private medical
  • Income protection plan
  • Holidays
  • Bike to work scheme
Read More
Arrow Right