Associate clinical trial Work, Jobs in London (with Salaries)

Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Master's degree
- Business development
- Psychology
- Annual leave
- Gym membership
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Nursing
- Doctoral degree
- Master's degree
Quick apply
Research Assistant or Associate for the PAiNTS human challenge study
Imperial College London —South Kensington
- £45,399 - £59,484 a year
- Full-time
- Hybrid work
- Doctoral degree
- Laboratory experience
- Research
5d
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
9d
Associate Practitioner
The Royal Marsden NHS Foundation Trust —Sutton
- £33,262 - £36,027 a year
- Full-time
- Laboratory experience
- Data entry
1d
Senior Clinical Research Associate
TFS HealthScience —London
- Part-time
- Remote
- Nursing
- Computer literacy
- English
Quick apply
2d
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Travel
Quick apply
Senior Analyst - BCG Vantage, Health Care - Biopharma R&D
Boston Consulting Group —London
- Full-time
- English
- Master's degree
- Travel
Business Development Associate
Medrio —London
- £45,000 - £48,000 a year
- Remote
- Salesforce
- Business development
- Presentation skills
Quick apply
Associate Director, Clinical Operations
TFS HealthScience —London
- Hybrid work
- Bachelor's degree
- Team management
- No degree
Quick apply
Research Associate (Mandarin Speaker)
Beacon Intelligence —London
- £27,000 a year
- Full-time
- Hybrid work
- Quality control
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
AWS Workspace Engineer- UK Remote
MEDIDATA —London
- AWS
- Communication skills
- Annual leave
Real World Data Strategy - Associate Consultant
ZS —London
- Hybrid work
- Doctoral degree
- English
- Master's degree
- Work from home
10d
Clinical Data Strategy, Manager
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation
Pharmaron —Hoddesdon
- Master's degree
- Bachelor's degree
- Mentoring
Senior Safety Scientist / Associate Director / Director
Roche —Welwyn
- Doctoral degree
- Master's degree
- Presentation skills
Associate Director - Healthcare Communications (DATA)
Burson Global —London
- Hybrid work
- Business development
- Mentoring
- Leadership
Associate Director, Global Medical Affairs (2-year contract)
BioNTech AG —London
- Full-time
- Doctoral degree
- Project management
- Travel
Associate Director, Regulatory Affairs
WEP Clinical —London
- Full-time
- Hybrid work
- Management
- Computer literacy
- Microsoft Office
- Employee assistance programme
10d
Research Associate in Host Immunity (FI/GSK)
Imperial College London —Hammersmith
- £45,399 - £59,484 a year
- Full-time
- Doctoral degree
- Research
- Mentoring
4d

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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

associate clinical trial jobs in london

Associate (Clinical Outcome Assessments - COA)

Drug Safety Associate II

Research Assistant or Associate for the PAiNTS human challenge study

Career Evening at Medpace London - Project Coordinator

Associate Practitioner

Senior Clinical Research Associate

Study Manager, Clinical Operations

Senior Analyst - BCG Vantage, Health Care - Biopharma R&D

Business Development Associate

Associate Director, Clinical Operations

Research Associate (Mandarin Speaker)

AWS Workspace Engineer- UK Remote

Real World Data Strategy - Associate Consultant

Clinical Data Strategy, Manager

Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation

Senior Safety Scientist / Associate Director / Director

Associate Director - Healthcare Communications (DATA)

Associate Director, Global Medical Affairs (2-year contract)

Associate Director, Regulatory Affairs

Research Associate in Host Immunity (FI/GSK)

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