Clinical research associate Work, Jobs in Notting Hill (with Salaries)

Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Master's degree
- Business development
- Psychology
- Annual leave
- Gym membership
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
3d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Research Associate in Translational Neuroimaging
Imperial College London —White City
- £50,733 - £52,675 a year
- Full-time
- Doctoral degree
- Research
- University
Associate Consultant - Value & Access
Lumanity —London
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Travel
Quick apply
Research Associate in Infectious Disease Modelling
Imperial College London —White City
- £50,733 - £59,484 a year
- Full-time
- Doctoral degree
- Travel
13d
Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- Research
- University
Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation
Pharmaron —Hoddesdon
- Master's degree
- Bachelor's degree
- Mentoring
Research Fellow in Brain Vascular Biology and Brain Cancer Biology
University College London —London
- £43,374 - £51,860 a year
- Full-time
- Doctoral degree
- English
- Research
- Annual leave
- Employee assistance programme
Associate Director, Precision Medicine (Clinical Diagnostics)
Regeneron —Uxbridge
- Doctoral degree
- Annual leave
Clinical Data Strategy, Manager
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
Associate Director, Clinical Trial Lead (all genders)
Merck KGaA —London
- Doctoral degree
- Master's degree
- Mentoring
Research Associate in Orthopaedic Surgical Robotics
Imperial College London —South Kensington
- £50,733 - £59,484 a year
- Full-time
- Hybrid work
- Doctoral degree
- Engineering
- Research
13d
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £230,000 - £270,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
Team Lead, Site Operations
ICON Plc —South London
- Full-time
- Bachelor's degree
- Team management
- Organisational skills
- Employee assistance programme
Senior Consultant Health Economist (Modeller)
Aquarius Population Health —London
- £63,000 - £73,000 a year
- Hybrid work
- Doctoral degree
- English
- Master's degree
6d
Market Research Associate (Danish Speaking) - Remote
M3EU —London
- Full-time
- Remote
- Computer literacy
- English
- Analysis skills
Quick apply

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Associate (Clinical Outcome Assessments - COA)

Clarivate -
London

Apply Now

Job details

Full-time

Benefits

Annual leave
Company pension
Private medical insurance
Gym membership
Life insurance

Qualifications

Report writing
Clinical research
Report generation
Microsoft Office Suite
Sociology
Master's degree
Business development
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

clinical research associate jobs in notting hill

Associate (Clinical Outcome Assessments - COA)

Career Evening at Medpace London - Project Coordinator

Clinical Research Associate I

Research Associate in Translational Neuroimaging

Associate Consultant - Value & Access

Study Manager, Clinical Operations

Research Associate in Infectious Disease Modelling

Associate Director / Associate Principal, Patient-centered Mixed Methods, Survey & Implementation Science Research

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences

Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

Associate Director, Precision Medicine (Clinical Diagnostics)

Clinical Data Strategy, Manager

Associate Director, Clinical Trial Lead (all genders)

Research Associate in Orthopaedic Surgical Robotics

Director, Portfolio Development Process & Standards Lead

Team Lead, Site Operations

Senior Consultant Health Economist (Modeller)

Market Research Associate (Danish Speaking) - Remote

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