Clinical research associate Work, Jobs in Banstead, Sry (with Salaries)

Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
8d
Research Associate
Imperial College London —South Kensington
- £43,863 - £57,582 a year
- Full-time
- Doctoral degree
- University
- Machine learning
7d
Clinical Research Fellow
University College London —London
- £48,705 - £69,584 a year
- Full-time
- Computer literacy
- Computer skills
- Communication skills
- Annual leave
- Employee assistance programme
9d
Research Fellow
University College London —London
- Full-time
- Doctoral degree
- Annual leave
- Employee assistance programme
11d
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Research Assistant Working Collaboratively with the Homeless Sector
University of Surrey —Guildford
- £36,636 a year
- Full-time
- Hybrid work
- Master's degree
- University
- Psychology
- Relocation assistance
- Annual leave
3d
Senior Clinical Research Associate - UK&IRE - 0.5FTE
ProPharma Group —London
- Part-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
11h
Senior Technician - Clinical Trials
The Royal Marsden NHS Foundation Trust —Sutton
- £36,943 - £44,900 a year
- Full-time
10d
Senior Data Manager / Clinical Trials Associate
University College London Hospitals NHS Foundation Trust —London
- £47,951 - £56,863 a year
- Full-time
- Organisational skills
- Leadership
- Communication skills
4d
Senior Clinical Research Fellow in Clinical Academic Networks and Grant Development
Kingston and Richmond NHS Foundation Trust —Kingston upon Thames
- £45,715 - £69,976 a year
- Part-time
- Doctoral degree
- Master's degree
- Project management
- Employee assistance programme
2d
Assistant Professor / or Associate Professor (Clinical & non clinical) in Public Health and Community Involvement
Imperial College London —White City
- £70,718 - £145,477 a year
- Full-time
- Doctoral degree
- University
- Leadership
Consultant (Clinical Outcome Assessment - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Doctoral degree
- Annual leave
- Gym membership
2d
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
Research Associate* in Trustworthy MRI Reconstruction with Uncertainty Modelling
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Doctoral degree
- Master's degree
- Analysis skills
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
- University
- Annual leave
- Employee assistance programme
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Manager - Patient Experience Data
IQVIA —London
- Project management
- IT
- Time management
Associate Director
Cancer Research UK —London
- Full-time
Associate Director, Translational Medicine Expert, TM Clinical Pharmacology
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Doctoral degree
- English
Trial Vendor Associate Director
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Communication skills

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clinical research associate jobs near banstead, sry

Associate (Clinical Outcome Assessments - COA)

Clarivate -
London

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Job details

Full-time
8 days ago

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.

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Refine Your Search

clinical research associate jobs in banstead, sry

Associate (Clinical Outcome Assessments - COA)

Research Associate

Clinical Research Fellow

Research Fellow

Clinical Trial Associate Manager

Research Assistant Working Collaboratively with the Homeless Sector

Senior Clinical Research Associate - UK&IRE - 0.5FTE

Senior Technician - Clinical Trials

Senior Data Manager / Clinical Trials Associate

Senior Clinical Research Fellow in Clinical Academic Networks and Grant Development

Assistant Professor / or Associate Professor (Clinical & non clinical) in Public Health and Community Involvement

Consultant (Clinical Outcome Assessment - COA)

Clinical Quality Assurance - Program Lead (Associate Director)

Research Associate* in Trustworthy MRI Reconstruction with Uncertainty Modelling

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

Clinical Trials Manager

Manager - Patient Experience Data

Associate Director

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

Trial Vendor Associate Director

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