Clinical associate Work, Jobs in Little Warley, Ess (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
Career Evening at Medpace London - Project Coordinator
Medpace, Inc. —London
- Full-time
- English
- Bachelor's degree
- Organisational skills
- Annual leave
- Work from home
2d
QA Associate
hVIVO Services Limited —London
- Administrative experience
PLOS Medicine Associate Editor- 12 Month FTC
Public Library of Science —London
- £35,000 - £47,000 a year
- Remote
- Doctoral degree
- Communication skills
QC Associate Role (Fixed Term)
Thermo Fisher Scientific —Bishop's Stortford
- Full-time
- Continuous improvement
- Quality control
Sector Advisor – BTEC Level 2 Diploma Healthcare Science
Pearson —London
- Remote
- Word processing
- Writing skills
Sector Advisor – BTEC Level 4 Diploma Healthcare Science
Pearson —London
- Remote
- Word processing
- Writing skills
End Point Assessor - Apprenticeship - Senior Healthcare Support Worker (Allied Health Profession Therapy Support) (Level 3)
Pearson —London
- Travel
- Conflict management
- Hospice
Specialist Tutors & Mentors
A Space To Thrive Ltd —London
- £38 - £43 an hour
- Full-time
- Hybrid work
- University
- Bachelor's degree
- Mentoring
Quick apply
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
Clinical Editor - BMJ Women's Health
BMJ —London
- £28,827 a year
- Hybrid work
- Bachelor's degree
- Analytics
- Employee discount
Quick apply
4d
ADHD Assessor - Associate Network
Healios —London
- Remote
- Experience working with children
- Flexible schedule
Quick apply
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —London
- Full-time
- Remote
- Leadership
Quick apply
Associate Director, Medical Information
EVERSANA —London
- Full-time
- Remote
- Doctoral degree
- English
- Research
- Annual leave
Quick apply
Associate Clinician - Autism Assessment (ADOS and ADI-R)
Healios —London
- Remote
- Google Suite
- Experience working with children
- Flexible schedule
Quick apply
Full Time CCA/PCA London Fields
Hello Vet —London
- £27,000 a year
- Full-time
- Front desk
- Employee assistance programme
10d
Head of People
Paloma Health —London
- £90,000 a year
- Full-time
- Hybrid work
- Human resources
- Recruiting
- Contracts
- Annual leave
- Employee assistance programme
3d
Associate Consultant - Value & Access
Lumanity —London
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree

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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 associate jobs in little warley, ess

Associate (Clinical Outcome Assessments - COA)

Drug Safety Associate II

Career Evening at Medpace London - Project Coordinator

QA Associate

PLOS Medicine Associate Editor- 12 Month FTC

QC Associate Role (Fixed Term)

Sector Advisor – BTEC Level 2 Diploma Healthcare Science

Sector Advisor – BTEC Level 4 Diploma Healthcare Science

End Point Assessor - Apprenticeship - Senior Healthcare Support Worker (Allied Health Profession Therapy Support) (Level 3)

Specialist Tutors & Mentors

Study Manager, Clinical Operations

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

Clinical Editor - BMJ Women's Health

ADHD Assessor - Associate Network

Associate Pharmacovigilance Project Manager (Europe)

Associate Director, Medical Information

Associate Clinician - Autism Assessment (ADOS and ADI-R)

Full Time CCA/PCA London Fields

Head of People

Associate Consultant - Value & Access

I want to receive the latest job alerts for clinical associate in little warley, ess

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