Pharmaceutical research and development Work, Jobs in London, Eng (with Salaries)

Research Associate
Lumanity —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Bachelor's degree
- Medical terminology
Quick apply
Healthcare Analyst
GlobalData Plc. —London
- £35,000 - £40,000 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
1d
Research Scientist, Radiobiology
Bicycle Therapeutics —London
- Full-time
- Hybrid work
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
8d
Senior Research Executive-Custom Healthcare research
Ipsos —London
- Microsoft Powerpoint
- Microsoft Excel
- Business development
- Annual leave
Senior Consultant and Statistician (Patient Centered Research) m/w/d
IQVIA —London
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Communication skills
Programme Manager
Life Arc —London
- Full-time
- Hybrid work
- Management
- Project management
- Bachelor's degree
- Annual leave
7d
Medical Writer
Lucid Group —London
- Full-time
- Hybrid work
- Agile
- Employee assistance programme
Senior Research Executive - Syndicated Healthcare
Ipsos —London
- Data analysis skills
- Microsoft Office
- Business development
- Annual leave
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
Principal - Health Economics and Outcomes Research (Market Access)
Ipsos —London
- Microsoft Excel
- Master's degree
- Business development
- Annual leave
Development Scientist
Haleon —Weybridge
- Full-time
- Computer literacy
- Bachelor's degree
10d
Central Laboratory Vendor/Project Manager - Remote - FSP
Parexel —Greater London
- Remote
- Management
- Laboratory experience
Research Manager-Syndicated Healthcare
Ipsos —London
- Microsoft Outlook
- Data analysis skills
- Microsoft Office
- Annual leave
10d
Medical Writing Associate
Cancer Research UK —London
- £30,000 - £36,000 a year
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
13h
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Microsoft Excel
Quick apply
Programme Manager
LifeArc —London
- Full-time
- Hybrid work
- Management
- Project management
- Bachelor's degree
- Annual leave
7d
Conflicts Analyst
Ropes & Gray LLP —London
- Customer service
- Bachelor's degree
- Data entry
Vice President (Life Sciences Strategy Consulting, Pharma Practice)
BGBx Consulting —London
- Data analysis skills
- Business development
- Bachelor's degree
- Annual leave
- Life insurance
Quick apply
Portfolio Innovation Director - Global Clinical Operations
Novartis —London
- £83,510 - £155,090 a year
- Full-time
- Hybrid work
- English
- Bachelor's degree
4d

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Research Associate

Lumanity -
London

Apply Now

Job details

Full-time

Benefits

Annual leave
Company pension
Private medical insurance
Car scheme

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Qualitative analysis
Master's degree
Administrative experience
IT
Project leadership
Leadership
Communication skills

Full job description

Overview / About us:

Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product, translate the science and data into compelling product narratives, and enable commercial decisions that position these products for success in the market. We do this through strategic and complimentary areas of focus: Asset Optimization and Commercialization, Value, Access, and Outcomes, Medical Strategy and Communications, and Real-World Evidence.

The Lumanity Patient-Centered Outcomes (PCO) team wishes to hire a Research Associate in this UK-based hybrid role.

Responsibilities / Position overview:

Targeted Literature Review Execution: Conducts defined steps of an established search strategy by applying specified screening criteria and extracting required data to meet the objectives of a targeted literature review.
Study Document Drafting & Revision: Drafts, revises, and quality checks study documents by using approved templates and incorporating direction from project leadership to align content with study scope and requirements.
Qualitative Interview Preparation & Conduct: Completes required training and conducts high-quality qualitative interviews with research participants (e.g., patients, caregivers) virtually or in person (travel required), adhering to the interview guide and study protocol.
Qualitative Coding & Analysis: Codes and analyzes qualitative participant-level data by applying a coding framework developed with guidance and oversight from the project lead.
Survey Implementation & Analysis: Executes defined steps of survey implementation and analysis by conducting pilot testing, quality checking survey data, analyzing open-ended items qualitatively, and producing descriptive analyses.
Client Meeting Participation & Documentation: Attends select client meetings (primarily virtual and occasionally in person) and captures discussion points, decisions, and next steps by producing clear, complete meeting minutes.
Deliverable Content Development: Drafts assigned portions of client deliverables (e.g., introduction, methods, and results sections) for presentations, reports, and memos by following guidance from the project lead.
Quality Management & Quality Control (QC): Operates within the PCO Quality Management System by following standard operating procedures, including using the QC checklist to reduce errors before deliverables are finalized.
Multi-Project Task Delivery: Delivers assigned tasks across multiple concurrent active projects by confirming requirements with project leads, managing personal deadlines, and communicating status to maintain project momentum.

Qualifications:

Undergraduate or Master’s degree in health-related field.
No prior full-time professional experience required; prior internship, academic research experience, or administrative coordination experience in a health, research, or clinical setting is preferred.
Working knowledge of core research fundamentals (e.g., study design, literature review methods, and data synthesis) sufficient to execute defined tasks with guidance.
Ability to complete required training and conduct qualitative interviews with research participants virtually and in person, including willingness and ability to travel as required.
Ability to code and analyze qualitative participant-level data, including experience with qualitative analysis software or a demonstrated ability and willingness to learn it quickly.
Experience executing targeted literature review tasks, including structured searching, applying inclusion and exclusion criteria, and extracting data into standardized formats.
Strong writing skills to develop assigned sections of client deliverables in a clear, client-ready format under direction from project leadership.
Professional communication skills for internal project work and client-facing interactions, including the ability to document discussions accurately in meeting minutes.
Proficiency with Microsoft Word, Microsoft PowerPoint, and Microsoft Excel.
Experience with qualitative analysis software or desire to learn.
Ability to manage workload across multiple concurrent projects (typically 8–10 active projects) while meeting deadlines and maintaining accuracy.
Awareness of the drug development process, including regulations that govern the pharmaceutical industry.

Benefits:

We offer our employees a comprehensive benefits package that focuses on what matters to you – health and well-being, personal finances, professional development, and a healthy work/life balance.

Competitive salary plus bonus scheme
33.5 days of paid leave annually
Generous pension scheme
Private healthcare
Electric Car scheme for those based in the United Kingdom
Remote or hybrid working (remote plus working out of one of our local offices in London or Sheffield)

Apply Now

Refine Your Search

pharmaceutical research and development jobs in london, eng

Research Associate

Content Writer - Pharmacovigilance

Healthcare Analyst

Research Scientist, Radiobiology

Senior Research Executive-Custom Healthcare research

Senior Consultant and Statistician (Patient Centered Research) m/w/d

Programme Manager

Medical Writer

Senior Research Executive - Syndicated Healthcare

GCP Compliance Manager - Clinical Programs & Trials

Principal - Health Economics and Outcomes Research (Market Access)

Development Scientist

Central Laboratory Vendor/Project Manager - Remote - FSP

Research Manager-Syndicated Healthcare

Medical Writing Associate

Medical Information Specialist - US Hours

Programme Manager

Conflicts Analyst

Vice President (Life Sciences Strategy Consulting, Pharma Practice)

Portfolio Innovation Director - Global Clinical Operations

I want to receive the latest job alerts for pharmaceutical research and development in london, eng

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