Clinical trials associate Work, Jobs in London, Eng (with Salaries)

Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —London
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Data analysis skills
CRA2 - Multi-Sponsor Department
IQVIA —London
- Full-time
- Remote
- No degree
- Work from home
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
Quick apply
Associate Director, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- In-person
CRA 2 - Single Sponsor Dedicated
IQVIA —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Professor in Implementation Science for Global Eye Health
London School of Hygiene & Tropical Medicine —London
- £64,469 - £73,994 a year
- Full-time
- Hybrid work
- Doctoral degree
- Annual leave
3d
Clinical Trials Research Nurse
The Princess Alexandra Hospital NHS Trust —Harlow
- £39,959 - £48,117 a year
- Travel
3d
Clinical Operations & Enablement Lead
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Presentation skills
- Bachelor's degree
Quick apply
Research Associate in Osteoarthritis Biostatistics
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Hybrid work
- Doctoral degree
- Computer skills
- Communication skills
10d
Associate Director, Clinical Operations
TFS HealthScience —London
- Hybrid work
- Bachelor's degree
- No degree
- Leadership
Quick apply
Data Associate
hVIVO Services Limited —London
- Microsoft Office
- Organisational skills
7d
Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —London
- £63,917 - £118,703 a year
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Associate Director, Medical Programs
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Project management
- Bachelor's degree
Quick apply
Senior Regulatory Associate
Pfizer —Walton-on-Thames
- Full-time
- Doctoral degree
- Marketing
- Computer literacy
4d
Senior Feasibility Associate / Feasibility Manager
Precision Medicine Group —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Data analysis skills

I want to receive the latest job alerts for clinical trials associate in london, eng

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trials associate jobs near london, eng

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

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

clinical trials associate jobs in london, eng

Associate (Clinical Outcome Assessments - COA)

Consultant (Clinical Outcome Assessment - COA)

Clinical Trials Manager

Drug Safety Associate II

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

CRA2 - Multi-Sponsor Department

Study Manager, Clinical Operations

Associate Director, Clinical Data Management

CRA 2 - Single Sponsor Dedicated

Associate Professor in Implementation Science for Global Eye Health

Clinical Trials Research Nurse

Clinical Operations & Enablement Lead

Research Associate in Osteoarthritis Biostatistics

Associate Director, Clinical Operations

Data Associate

Clinical Quality Assurance - Program Lead (Associate Director)

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Associate Director, Medical Programs

Senior Regulatory Associate

Senior Feasibility Associate / Feasibility Manager

I want to receive the latest job alerts for clinical trials associate in london, eng

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected