Evidence Synthesis Manager Job at SRG (Berkshire)

Associate Director – Value Communication and Evidence Synthesis

As Associate Director – Value Communication & Evidence Synthesis, you will play ...

Location

United Kingdom

Salary:

Not provided

Bioscript Group

Expiration Date

Until further notice

Requirements

Postgraduate degree (MSc or PhD) in Health Economics, Public Health, Epidemiology, Biostatistics, or related life sciences discipline
7+ years in market access, value communication, HEOR, or HTA consulting, with proven ability to lead complex, multi-disciplinary projects
Deep understanding of global HTA processes, payer evidence requirements, and market access dynamics
Demonstrated experience in evidence generation and synthesis, including systematic literature reviews, indirect treatment comparisons, and meta-analyses
Excellent analytical and writing skills, with the ability to distil complex data into actionable insights
Strong project and client management skills, with experience overseeing multiple projects and engaging senior stakeholders
Proven leadership and people management abilities, with a track record of mentoring and developing high-performing teams
Effective communicator with confident presentation skills and the ability to build trusted relationships with clients and colleagues
Experience contributing to business development, including proposal development and client pitches

Job Responsibility

Lead and deliver a diverse portfolio of projects across value communication, evidence synthesis, and HTA
Provide scientific and strategic oversight for the design, execution, and quality assurance of deliverables, including: global value dossiers, payer and reimbursement submissions, systematic and targeted literature reviews (SLRs, TLRs), evidence synthesis and meta-analyses (including ITCs and NMAs)
Translate complex data and analyses into clear, evidence-based narratives aligned with payer and stakeholder needs
Oversee multiple project teams, ensuring deliverables are completed on time, within budget, and to the highest quality standards
Manage project resourcing, timelines, and workload allocation to optimise team performance and impact
Line manage and mentor consultants and analysts, providing technical guidance and supporting professional growth
Foster a high-performance culture focused on collaboration, learning, and continuous improvement
Strengthen team capability in HTA, HEOR, and evidence synthesis methodologies
Collaborate across Valid Insight’s three core pillars—Strategy, Evidence Synthesis, and Value Communication—to deliver integrated, end-to-end market access solutions
Work with cross-functional teams within the Bioscript Group to leverage shared expertise and enhance project delivery

What we offer

Competitive salary package
Flexible and remote working options
Generous annual leave policy which includes a winter shutdown
Birthday charity donation to a charity of your choice
Bonus Day off for community volunteering
Opportunities for professional development and career progression

Fulltime

New

Health Economics Consultant (Evidence Evaluation)

As part of Parexel Consulting, you will play a vital role in helping biopharmace...

Location

India , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Training/experience in health economics and/or outcomes preferred
Minimum 5 years of experience in a relevant role preferred
Experience in Health Economics Outcomes Research (HEOR) and Systematic Literature Review (SLR), or evidence evaluation environments
Master's degree or equivalent in Life Science/MBBS/BDS/PhD is essential
Strong computing skills (MS Office)
High analytical ability
High degree of written accuracy and attention to detail
Strong oral and written communication of technical information
Self-motivation and enthusiasm
Flexible attitude for new learning and varied tasks

Job Responsibility

Provide high-quality, timely, scientific/strategic solutions to meet client needs
Understand client objectives and customize evidence delivery using innovative strategies
Lead conduct and analysis of research to shape strategic recommendations under guidance of Project Director
Manage and execute Systematic Literature Review (SLR) tasks: screening, data extraction, protocol design, quantitative feasibility
Prepare synthesis and review of findings
Develop SLR deliverables: reports, slide decks, manuscripts, abstracts, posters
Produce quality work aligned with expectations of Project Lead/Manager and clients
Work within broad project guidelines under Project Director/Technical Subject Matter Experts (SMEs)
Take initiative to prioritize work while aligning with Project Lead and Line Manager
Follow and implement organization’s consulting models and methodologies

Scientific Coordinator Science-Policy Interface

The Scientific Coordinator is responsible for the gathering, synthesising and de...

Location

France , Paris

Salary:

3470.00 - 3560.00 EUR / Month

WOAH - World Organisation for Animal Health

Expiration Date

June 29, 2026

Requirements

A graduate degree in veterinary sciences (DVM)
At least 10 years of professional experience in animal health, veterinary public health, epidemiology, or related fields with at least 3 years of international experience
Professional experience within Veterinary Services, competent authorities, or areas related to international trade of animals and animal products (e.g., SPS measures, import/export controls, risk analysis)
Demonstrated experience working at the science–policy interface, including the translation of scientific evidence into policy-relevant outputs
Experience participating in, supporting, or coordinating expert groups, scientific committees, or technical advisory processes
Excellent scientific and technical writing skills including risk assessment principles, and WOAH’s mandate
Strong skills in evidence assessment, including literature review, data interpretation, and synthesis of complex scientific topics
Good working knowledge of Microsoft 365
Excellent knowledge of English, both spoken and written
Good knowledge of French or Spanish (desirable)

Job Responsibility

Collect and Synthesise Scientific Information
Support the Work of ad hoc Groups of experts
Support the Secretariat of the Specialist Commissions
Provide support to the work of the Department

What we offer

Salary is exempt from income tax in France

Fulltime

Senior User Researcher

Whitehall Resources are looking for a Senior User Researcher. This role is hybri...

Location

United Kingdom , London

Salary:

Not provided

Whitehall Resources Ltd

Expiration Date

Until further notice

Requirements

Genuine user/customer engagement experience (could be industry like market research, field research)
Public Sector experience as user researcher is important, as would experience of taking digital services through GDS assessments – taking a service from Discovery, Alpha, Beta and into Live
Empathetic, human-centred design led thinker (vs. requirements/business analyses type user engagement)
Evidence of working in multidisciplinary team and working with Product Managers, Content Designers, Interaction Designers Analysis and synthesis
You can turn research data into clear findings that inform decisions. You know how to involve colleagues in analysis and synthesis to increase consensus and challenge assumptions
Inclusive research- You understand the diversity of users of government services. You know how to include all kinds of users in appropriate research activities to help teams deliver accessible services
Research skills – You understand and have experience of a range of user research methods. You can choose appropriate methods for different stages of the product life cycle and situations. You know how to apply methods correctly
Society and technology – You understand the social and technological context for government services. You can help colleagues understand how digital technology is changing user behaviour, and the challenges and opportunities for government services
Strategic insight – You understand organisational strategy and objectives. You can align user research activities with objectives to create strategic insights that inform policy and proposition
Technical understanding – You demonstrate knowledge of the technologies used to build and operate digital services. You understand the different technical roles in a multidisciplinary team

Medical Librarian I

The Medical Librarian is a key member of Boston Children's Hospital's Research I...

Location

United States , Boston

Salary:

52228.80 - 83564.00 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Master's degree in Library and Information Science, Information Science, Biomedical Informatics, or a closely related field
Prior experience in a biomedical, academic, hospital, or research library is preferred but not required
Strong interest in biomedical research, clinical information services, scholarly communication, and modern library services
Familiarity with medical literature databases, citation management tools, point-of-care resources, or digital library systems
Interest in emerging digital tools, AI-enabled discovery platforms, and modern research workflows
Excellent written, verbal, organizational, and customer service skills
Ability to learn quickly, take initiative, work collaboratively, and grow rapidly into the role
Strong attention to detail and comfort preparing user guides, training materials, and presentations
Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook

Job Responsibility

Provide expert literature search support for clinicians, researchers, and staff, including development of structured search strategies for research projects, evidence reviews, grant applications, and publication support
Develop, maintain, and assess access to the library's core portfolio of search platforms, journals, databases, point-of-care tools, citation managers, and related discovery services
Deliver individual and group training on medical literature databases, citation management systems, evidence synthesis methods, current awareness tools, and other research support technologies
Build advanced digital services that may include AI-assisted discovery workflows, literature surveillance, natural language processing and summarization awareness, alerting and RSS strategies, and programmatic retrieval using APIs where appropriate to the service model
Advise researchers and staff on publication and dissemination best practices, including public-access requirements, appropriate repositories, author identity and persistent identifiers, and methods for increasing discoverability and impact
Provide or coordinate guidance on research data management, data management and sharing plans, repository selection, and reproducible documentation of methods and protocols
Evaluate new and existing tools for accuracy, usability, accessibility, privacy, interoperability, licensing fit, and workflow relevance in a pediatric clinical and research environment
Coordinate access questions involving Harvard-affiliated resources, remote authentication, shared platforms, proxy or sponsored-access arrangements where applicable, and interlibrary loan and document-delivery pathways
Represent the library in presentations, committees, and collaborative initiatives across the hospital and affiliated environments
Use service data, user feedback, and usage metrics to assess outcomes, improve workflows, and communicate library value to Research Informatics and hospital leadership

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Senior Manager, Medical Affairs

As the Senior Manager, UCAN Medical Affairs, you will play a pivotal leadership ...

Location

United States , Deerfield

Salary:

160000.00 - 220000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Advanced healthcare degree with 8+ years of clinical experience
Background in ICU, Med-Surg, or Clinical Informatics strongly preferred
Prior Medical Affairs experience highly desirable
Proven experience within the healthcare or life sciences industry
Strong leadership, interpersonal, analytical, and problem-solving skills
Clinical trial experience with a solid understanding of Good Clinical Practice (GCP)
Working knowledge of biostatistics and clinical trial design
Expertise in literature review, synthesis, and scientific analysis
Confidence and effectiveness in public speaking and scientific presentations
Ability to travel up to 50%

Job Responsibility

Provide regional Medical Affairs leadership for new product development, ensuring scientific rigor and clinical relevance
Identify evidence-generation gaps and drive regional evidence strategies in alignment with Global Medical Affairs
Develop and execute scientific communication and non-promotional education plans supporting product and portfolio strategy
Lead and support advisory boards, investigator meetings, roundtables, and scientific forums
Partner cross-functionally to shape long-term Medical Affairs strategies and thought leader engagement plans
Represent Medical Affairs at medical congresses, translating emerging data into actionable insights
Monitor scientific trends and oversee regional activities including grants, sponsorships, and Investigator-Initiated Research
Contribute to clinical and scientific training while building a strong NPE offering for the UCAN HST portfolio
Lead, coach, and develop the Medical Science Liaison (MSL) team
Establish and execute strategies for Key Opinion Leader (KOL) identification, development, and engagement

What we offer

Medical and dental coverage that start on day one
Basic life insurance
Accident insurance
Short-term and long-term disability insurance
Business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays

Fulltime

Manager, Product Design

Bentley Systems is the infrastructure engineering software company, advancing th...

Location

Canada , Toronto

Salary:

Not provided

Bentley Systems

Expiration Date

Until further notice

Requirements

8+ years in UX, UI, or Product Design, with 3+ years managing or leading designers
Experience leading transformation-scale design work – consolidating experiences, rethinking journeys end to end, and bringing cross-functional teams along for the ride
Strong track record contributing to digital buying or growth experiences – ecommerce, conversion flows, content-led journeys, or equivalent
A genuine people leader who invests in their team's growth, creates clarity, and holds high standards without creating fear
Strong facilitation skills – you know how to create alignment across functions and turn ambiguity into a shared direction
Comfortable working within a broader strategic framework – translating vision into delivery and keeping the team focused on the right problems
A solid foundation across UX, UI, and interaction design – enough to coach others, spot quality issues, and know when to bring in specialist support
Strong communication and storytelling skills – you make complexity accessible without oversimplifying it
A practical, data-informed approach: you know when to follow the data and when to push back on it
Fluency in modern design tools (Figma, Miro, Adobe CC) and genuine curiosity about how AI is changing the craft

Job Responsibility

Lead and develop the team: Coach and develop your Designers through regular 1:1s, honest feedback, and genuine investment in their careers. Create the conditions for great work — shared clarity on priorities, the safety to experiment, and high standards for craft. Contribute to hiring, onboarding, and supporting performance across the portfolio
Drive experience transformation: Lead the Design work to consolidate and reimagine Bentley's buying experiences — bringing fragmented journeys together into something coherent, considered, and conversion-focused. Use design thinking and facilitation to align teams and turn that alignment into experiences that are clear, trustworthy, and effective at every touchpoint
Drive outcomes, not just outputs: Work cross-functionally to define what good looks like — conversion, engagement, drop-off, user confidence — and connect your team's design decisions directly to those metrics. Draw on data and user insight to understand where experiences are underperforming and why. Make outcome-thinking part of how the team works every day
Own discovery and delivery: Hold both ends of the process with equal rigour. Discovery means deeply understanding the problem before designing the solution — through research, usability evaluation, and talking to real users. Delivery means shipping work that performs, iterating based on evidence, and maintaining quality under pressure. Your laser focused on building a team that does both well
Raise the bar for design quality: Set high expectations across UX, UI, interaction design, IA, accessibility, and content clarity. Coach designers to think about the person on the other side — their psychology, their hesitations, the moments where trust is won or lost. Contribute to the design system as a foundation for consistency and scale
Build a culture of experimentation: Make testing and learning a normal part of how the team works — not an exception. Create space for fast, low-cost experiments and use what you find to make better decisions faster
Be a strong collaborative voice across disciplines: Communicate decisions, trade-offs, and rationale clearly — in commercial rooms and design rooms alike. Bring the user perspective into every shared conversation and help the wider team make better decisions because design is at the table
Help define design in an AI-augmented world: Help your team explore and integrate AI tools in ways that genuinely improve the work — faster exploration, sharper synthesis, less time on repetitive production. And be the person leading the charge on where AI helps, and where human judgment needs to lead?

What we offer

Step into a collaborative work environment where ideas flourish, and teamwork propels us forward towards shared success
An attractive salary and benefits package
Bentley Impact Day: take a day off from work to volunteer with an organization of your choice
Celebrate milestone achievements and moments that matter through our colleague recognition award programs and our Bentley Achievers platform
A commitment to inclusion, belonging and colleague wellbeing through global initiatives and resource groups
Be part of a company committed to making a real difference by advancing the world’s infrastructure for better quality of life, where your contributions help build a more sustainable, connected, and resilient world

Fulltime

US Medical Affairs Lead, Oncology - Lung

The US Medical Affairs Lead (MAL), Lung is the single point of medical accountab...

Location

United States , Durham; Philadelphia

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Advanced scientific or clinical degree such as MD, PharmD, PhD, or equivalent
Eight or more years of Oncology experience in Medical Affairs, including US launch or launch preparation experience
Three or more years of experience shaping clinical trial design to fit US Market needs
Five or more years of experience developing medical strategy and evidence generation plans, and to deliver against asset operational plans

Job Responsibility

Accountable for development and execution of US medical strategy for lung oncology pipeline assets, ensuring alignment with asset strategy and Emerging Therapeutic Area priorities
Leads the US Medical Affairs Plan and Medical Matrix Team, adapting global strategy to US clinical practice, research infrastructure, and stakeholder needs
Represents the US medical perspective on Global Medical Teams, providing a strong US voice on unmet need, trial feasibility, and external expert expectations
Partners closely with Clinical Development to inform protocol design, eligibility criteria, endpoints, and site selection to optimize US relevance and enrollment
Drives systematic generation, synthesis, and communication of US medical insights from investigators, HCPs, and research networks
Provides strategic direction to Lung MSLs on engagement priorities, insight focus areas, and ISS/SCS concepts aligned to US medical strategy
Works with Value Evidence & Outcomes partners to identify US evidence gaps and shape local evidence generation plans
Ensures high‑quality, compliant medical engagement with external lung oncology experts and cooperative groups
Manages budget and spend for assigned lung oncology assets in accordance with governance requirements
Applies sound medical governance and is accountable for medical review, approval, and compliance oversight for assigned assets

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Select Country

Evidence Synthesis Manager

Job Description

Job Responsibility

Requirements

Looking for more opportunities?