Document reviewer Work, Jobs in England (with Salaries)

Associate II, TMF Operations - UK - Remote
Worldwide Clinical Trials —England
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Administrative experience
OCC Communications Officer
Warwickshire Police —Warwick
- £36,505 a year
- 12 hour shift
- Free parking
- Annual leave
Mortgage & Protection File Reviewer - MI280526
Mortgage Intelligence —Bournemouth
- £25,000 - £27,000 a year
- Hybrid work
- No experience needed
- IT
- Phone etiquette
- Annual leave
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
Final Reviewer & Certification Decision Maker
SGS —Frimley
- Full-time
- Hybrid work
- English
- University
- In-person
- Flexible schedule
Quick apply
Documentation Controller and Training Coordinator
Elanco —Speke
- Full-time
- Customer service
- Microsoft Office
- Continuous improvement
Document Controller
Dragados —London
- Full-time
- Microsoft Office
- SharePoint
- IT
Quick apply
Staff ML Systems Engineer - Media Intelligence
Tether Operations Limited —London
- Full-time
- Remote
- Azure
- System design
- English
Evidence and Evaluation Manager
Biotechnology and Biological Sciences Research Council —Swindon
- £46,743 a year
- Part-time
- Hybrid work
- Analysis skills
- Presentation skills
- Communication skills
- Annual leave
11d
Evidence and Evaluation Manager
UK Research and Innovation (UKRI) —Swindon
- £46,743 a year
- Full-time
- Hybrid work
- Analysis skills
- Communication skills
- Annual leave
- Employee assistance programme
Principal Data Scientist
CoMind —London
- £152,000 - £190,000 a year
- Full-time
- IT
- AI
- Leadership
- Employee discount
Social Impact Reporting and Operations Analyst
Fitch Group —London
- Microsoft Excel
- Analysis skills
- APIs
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £230,000 - £270,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
Technical Author
Watson Marlow Fluid Technology Solutions —Redruth
- English
- Project management
- Annual leave
Design Assurance Coordinator
SCS Railways —London
- Civil engineering
- Microsoft Excel
- Engineering
2d
Cyber & eDiscovery Expert
Forcyd —London
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Travel
- Flexible schedule
Quick apply
Technical Author
Watson-Marlow Fluid Technology Solutions —Falmouth
- English
- Project management
- Annual leave
Business Development Representative
FloQast —London
- Full-time
- Salesforce
- Accounting
- Communication skills
Junior Information Manager
Assystem —Bristol
- Engineering
- Project management
- Communication skills
Quality Advisor
CAD and ProjectWise System Administrator - Austin locations Austin, TX posted on Publicado hace más de 30 días Ferrovial Construction —Heathrow
- Full-time
- Computer literacy
- Communication skills

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Associate II, TMF Operations - UK - Remote

Worldwide Clinical Trials -
England

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
Clinical research
Administrative experience
Organisational skills
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

Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP) and working practices.

Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio of studies both in an electronic and hard copy format.

Prepare periodic TMF Quality Control checklists for review by Project Team review.

Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices.

Work with a variety of Electronic Document Management and electronic TMF Systems to review, classify and process Essential Documents

What you will bring to the role

Possess data collection, indexing and editing skills, including ability to adhere to standardized document naming conventions

Possess excellent written and verbal communication skills to clearly and concisely present information

Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment

Handle multiple, highly detailed tasks with exceptional accuracy. Demonstrate strong planning and organizational skills

Demonstrate proficiency in Microsoft Word and Excel

Develop proficiency in use of an electronic document repository or eTMF. General understanding of clinical research principles and processes

Your experience

Minimum 6 months of administrative experience, preferably but not strictly in the CRO or Pharma industry

Knowledge of working within a highly regulated industry (desirable)

A strong, long ‑ term interest in administrative ‑ focused work, with close attention to detail and comfort handling routine, process ‑ driven tasks

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

document reviewer jobs in england

Associate II, TMF Operations - UK - Remote

OCC Communications Officer

Mortgage & Protection File Reviewer - MI280526

Associate (Clinical Outcome Assessments - COA)

Final Reviewer & Certification Decision Maker

Documentation Controller and Training Coordinator

Document Controller

Staff ML Systems Engineer - Media Intelligence

Evidence and Evaluation Manager

Evidence and Evaluation Manager

Principal Data Scientist

Social Impact Reporting and Operations Analyst

Director, Portfolio Development Process & Standards Lead

Technical Author

Design Assurance Coordinator

Cyber & eDiscovery Expert

Technical Author

Business Development Representative

Junior Information Manager

Quality Advisor

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