Senior clinical research associate Work, Jobs in England (with Salaries)

Senior Associate I, TMF Operations - UK - Remote
Worldwide Clinical Trials —England
- Full-time
- Remote
- Microsoft Word
- Bachelor's degree
- Quality control
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Associate Director, Clinical Operations
Jazz Pharmaceuticals —Cambridge
- Remote
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
Senior Site Contracts Associate, IQVIA Biotech - UK
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- Presentation skills
- Bachelor's degree
- Work from home
2h
Research Associate/Senior Research Associate in Evidence Synthesis
University of Bristol —Clifton
- £39,096 - £50,253 a year
- Part-time
- Hybrid work
- Doctoral degree
- University
- School
8d
Senior Clinical Research Associate
TFS HealthScience —London
- Part-time
- Remote
- Nursing
- Computer literacy
- English
Quick apply
1d
Research Associate (ADHD Project)
Manchester Metropolitan University —Manchester
- £35,608 - £39,906 a year
- University
- Presentation skills
- Travel
- Life insurance
8d
Research Assistant / Research Associate in Systematic Reviewing
University of Sheffield —Sheffield
- £32,080 - £51,753 a year
- Full-time
- Hybrid work
- Doctoral degree
- Research
- Master's degree
- Annual leave
- Employee discount
4d
Healthcare Analytics & Insights Associate
ReportedHealth —Leeds
- Up to £38,000 a year
- Part-time
- Microsoft Powerpoint
- Data analysis skills
- Business development
Quick apply
6d
Associate Director, Patient-Centered Outcomes (PCO)
Jazz Pharmaceuticals —Cambridge
- £172,000 - £258,000 a year
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
- Annual leave
2d
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —London
- Full-time
- Remote
- Leadership
Quick apply
Senior Associate, Clinical Excellence
Reckitt —Kingston upon Hull
- Employee assistance programme
- Life insurance
Senior Research and Development Scientist
Leica Biosystems —Newcastle upon Tyne
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Research Associate/ Senior Research Associate (Fixed Term)
University of Cambridge —Cambridge
- £37,694 - £59,966 a year
- Hybrid work
- University
- School
3d
Senior Analyst - BCG Vantage, Health Care - Biopharma R&D
Boston Consulting Group —London
- Full-time
- English
- Master's degree
- Travel
Associate Professor (Education) in Clinical Pharmacy - Department of Pharmacy - 49782 - Grade 9
University of Birmingham —Birmingham
- £58,225 - £87,974 a year
- Full-time
- Management
- Doctoral degree
- Research
10d
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- Research
- University
Onsite Sr. Associate, Research Services
Avantor —Cambridge
- Full-time
- Databases
- Bachelor's degree
- No degree
- Flexible schedule
2d
Senior eCOA Screenshot Review Associate
ICON Plc —Reading
- Full-time
- Analysis skills
- Bachelor's degree
- No degree
- Employee assistance programme
3d

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senior clinical research associate jobs near england

Senior Associate I, TMF Operations - UK - Remote

Worldwide Clinical Trials -
England

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Document control
Record keeping
Spreadsheets
Bachelor's degree
Quality control
Organisational skills
Clinical trials
Document management
Communication skills

Full job description

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Records Management Compliance Department does at Worldwide

TMF Operations handles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout Worldwide Clinical Trials, our culture of collaboration and innovation is what propels us in our pursuit of excellence in clinical research and making a meaningful impact on every patient's life. Roles within our TMF Operations department have a global scope, with the opportunity to regularly collaborate with members of the Worldwide Project Team.

What you will do

Perform RMC Lead Activities for 1-3 Studies.

Support TMF set-up, coordinate ‘Requests for Sites to be added in eTMF’ between Project. Teams (PT) and eTMF administrators; review eTMF access and coordinate updates, as necessary.

Provide Subject Matter Expert (SME) support for Project Teams and Sponsor related to TMF.

Oversee the QC process and makes sure the RMC is on track (compliant with timelines and documentation) and follow up on non-compliance accordingly.

Prepare, maintain , and share TMF metrics and spreadsheets for assigned studies with Project Teams and Sponsors. Review TMF Key Performance Indicators (KPIs) and makes sure that TMF KPIs are in compliance .

Support Regulatory and Sponsor audits and audits finding resolution, where necessary.

What you will bring to the role

Excellent written and verbal communication skills to clearly and concisely present information

Strong interpersonal skills

Ability to handle multiple, highly detailed tasks with exceptional accuracy.

Strong planning and organizational skills

Proficiency in Microsoft Word and Excel

Your experience

University Degree preferred ( Life Science desirable )

1-3 years of relevant experience

Knowledge of working within a highly regulated industry or experience of CRO/Pharmaceutical Company industry

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .

Apply Now

Refine Your Search

senior clinical research associate jobs in england

Senior Associate I, TMF Operations - UK - Remote

Local Study Associate Director

Associate Director, Clinical Operations

Senior Site Contracts Associate, IQVIA Biotech - UK

Research Associate/Senior Research Associate in Evidence Synthesis

Senior Clinical Research Associate

Research Associate (ADHD Project)

Research Assistant / Research Associate in Systematic Reviewing

Healthcare Analytics & Insights Associate

Associate Director, Patient-Centered Outcomes (PCO)

Associate Pharmacovigilance Project Manager (Europe)

Senior Associate, Clinical Excellence

Senior Research and Development Scientist

Senior Clinical Research Associate

Research Associate/ Senior Research Associate (Fixed Term)

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

Associate Professor (Education) in Clinical Pharmacy - Department of Pharmacy - 49782 - Grade 9

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

Onsite Sr. Associate, Research Services

Senior eCOA Screenshot Review Associate

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