Remote clinical research associate Work, Jobs in London (with Salaries)

Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
PLOS Medicine Associate Editor- 12 Month FTC
Public Library of Science —London
- £35,000 - £47,000 a year
- Remote
- Doctoral degree
- Communication skills
Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
Market Research Associate (Danish Speaking) - Remote
M3EU —London
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
Quick apply
Clinical Operations & Enablement Lead
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Presentation skills
- Bachelor's degree
Quick apply
Market Research Associate (Dutch AND French speaking) Remote
M3EU —London
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
Quick apply
Associate Director, Qualitative Research
M3EU —London
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Quick apply
Associate Director, Regulatory Diagnostics
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Communication skills
- Negotiation
Trial Vendor Associate Director
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Communication skills
Associate Director, Global Publications & Foundational Content
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Communication skills
17h
Self-Employed Children and Young People ADHD Prescriber - Remote
CareADHD —Canary Wharf
- £37 - £74 an hour
- Temporary
- Remote
- Communication skills
Quick apply
Global Labelling Associate Director, Content (Established Products)
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Continuous improvement
Associate Director, Medical Programs
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Project management
- Bachelor's degree
Quick apply
Associate Director, Statistical Programming
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Nursing
- Computer Science
- Organisational skills
Director, Therapeutic Area Biomarker Lead (Neuroscience)
Novartis —London
- £83,510 - £155,090 a year
- Full-time
- Hybrid work
- Management
- Doctoral degree
- English
11d
Associate Director, Medical Safety Assessment Physician, Cell Therapy
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Analysis skills
- Travel
- In-person
5d
Head of Study, Site Management and Monitoring
Ipsen Biopharm Ltd —London
- Full-time
- Doctoral degree
- English
- Master's degree
Senior Medical Science Liaison EMEA
Terumo —London
- Doctoral degree
- Sales
- English
Senior Principal Statistical Programmer
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- Bachelor's degree

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PLOS Medicine Associate Editor- 12 Month FTC
Public Library of Science —Cambridge
You will collaborate with PLOS operations teams and vendors to ensure smooth and efficient manuscript processing, and to deliver an outstanding experience for…
£35,000 - £47,000 a year

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Associate (Clinical Outcome Assessments - COA)

Clarivate -
London

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Job details

Full-time

Benefits

Annual leave
Company pension
Private medical insurance
Gym membership
Life insurance

Qualifications

Microsoft Powerpoint
Report writing
Sociology
Microsoft Office
Master's degree
Psychology
Organisational skills
Communication skills
FDA regulations
Time management

Full job description

We are seeking a London, Hybrid based Associate (Clinical Outcome Assessments - COA) to serve as a critical member of project teams by providing analytical insight, leadership and creativity to billable client engagements, business development efforts and internal initiatives.

The Associate will help to define projects, build work plans, and develop robust and valuable conclusions and recommendations for our clients. Associates are vital to ensuring that we provide our clients with the insights and information they need to achieve success.

This role is focused in a high-growth area of the consulting business; the Clinical Outcome Assessment (COA) team. You will be expected to:

Contribute to projects focused on the development, evaluation, and implementation of COA research including Patient Reported Outcomes (PROs).
Provide research support in all aspects of project delivery including qualitative and quantitative data collection, data analysis, report writing, and writing abstracts and manuscripts

About You – experience, education, skills, and accomplishments

A master’s degree in health psychology, psychology, sociology, life sciences or other relevant topic (a 2:1 or higher)
Experience in qualitative and quantitative research methods
Proven experience in MS office suite including Excel, PowerPoint, and Word
At least 6 months experience working in a team (either vocational or academic)
Excellent verbal and written communication
Ability to work on multiple projects and prioritize workload
Good time management and organizational skills
Attention to detail
Hard-working with a commitment to high-quality deliverables
Ability to work within a team
Ability to work proactively and on own initiative and actively solve problems when required

It would be great if you also have:

Experience in outcomes research and/or patient-reported outcomes development and evaluation (desired but not critical)
Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance
Knowledge of the pharmaceutical/medical device industry and the client's operating environment

What will you be doing in this role?

Conduct research to produce consistently high-quality deliverables including:
- Develop qualitative and quantitative research study protocols and associated documents including interview guides and informed consent forms
- Conduct literature and instrument reviews including development of search strategy protocols, citation screening, literature review, development of data extraction tables, and review of social media data where appropriate
- Plan and conduct reviews of relevant COA/PRO instruments according to scientific and regulatory guideline
- Plan and conduct competitor landscaping activities e.g., review of PROLabels, clinicatrials.gov, EPARs, approved FDA and EMA labels, and regulatory meeting minutes and communications
- Plan and conduct qualitative interviews/focus groups with patients, clinicians, caregivers, and other relevant stakeholder groups
- Report writing and delivery of findings (Word/PowerPoint)
- Distil key messages from data analysis and write recommendations
Attend and present at client meetings
Attend training as required
Work with project team to meet project deadlines and achieve project objectives
Effective and timely administration (conform to house styles and processes)

About the Team :
Our team consists of 30+ outcomes researchers who have extensive methodological and commercial experience. We are experienced in the design, validation, and implementation of PRO measures and other COA instruments for clinical trials and clinical practice, with a focus on FDA, EMA, and HTA bodies. We have significant experience across a range of therapy areas, such as rare disease, oncology, immune disorders, respiratory, psychiatry, CNS, autoimmune, infectious diseases, pain, and women's health. Supported by a global multi-disciplinary team from the wider Clarivate team, we can involve medical writers, health economists, systematic reviewers, and strategic advisors in our projects as needed. Together, our experts provide integrated health economics and outcomes research (HEOR) and market access solutions across the product life cycle.

Hours of Work

This is a full-time permanent position based in London, UK and will require hybrid working in our Liverpool Street office (2-3 days per week in office, rest of week remote).

This position requires weekday (Monday - Friday) attendance with some scheduling flexibility available around core working hours.

Our UK Employee Benefits include :

Private Medical Insurance or Health Cash plan
Generous Pension Plan contribution rates
Income protection insurance
Life insurance
Sports Club Subsidy (Company pays 50% of gym membership, or up to £500)
Emergency Childcare or Adult care cover
Eyecare vouchers
From 25 Days Annual Leave + 8 Bank Holidays (option to buy and sell Annual leave)

#LI-Hybrid, #LI-Onsite #LI-SK1

At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

Apply Now

Refine Your Search

remote clinical research associate jobs in london

Associate (Clinical Outcome Assessments - COA)

PLOS Medicine Associate Editor- 12 Month FTC

Consultant (Clinical Outcome Assessment - COA)

Market Research Associate (Danish Speaking) - Remote

Clinical Operations & Enablement Lead

Market Research Associate (Dutch AND French speaking) Remote

Associate Director, Qualitative Research

Associate Director, Regulatory Diagnostics

Trial Vendor Associate Director

Associate Director, Global Publications & Foundational Content

Self-Employed Children and Young People ADHD Prescriber - Remote

Global Labelling Associate Director, Content (Established Products)

Associate Director, Medical Programs

Associate Director, Statistical Programming

Director, Therapeutic Area Biomarker Lead (Neuroscience)

Associate Director, Medical Safety Assessment Physician, Cell Therapy

Head of Study, Site Management and Monitoring

Senior Medical Science Liaison EMEA

Senior Principal Statistical Programmer

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