Research operations occupations Work, Jobs in Middlesex, Gtl (with Salaries)

Study Owner, eClinical Services
TransPerfect —London
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Communication skills
Quick apply
Research and insights manager
Sense —London
- £49,949 a year
- Full-time
- Hybrid work
- Organisational skills
5d
Research Support Officer
Imperial College London —South Kensington
- £41,005 - £45,616 a year
- Full-time
- Microsoft Outlook
- Travel
- Communication skills
- Annual leave
1d
Study Research Assistant
University College London —London
- £39,148 - £41,833 a year
- Full-time
- Bachelor's degree
- No degree
- Organisational skills
- Annual leave
- Employee assistance programme
2d
Research Coordinator (PAFTOL Project)
Kew Gardens —Kew Gardens
- £39,243 - £42,154 a year
- Full-time
- Laboratory experience
- Master's degree
- Annual leave
- Employee assistance programme
12d
Senior Research Operations Coordinator
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Bachelor's degree
- IT
- Annual leave
- Employee assistance programme
2d
Translational Study Coordinator
ICR —London
- £31,445 - £33,100 a year
- Organisational skills
11d
Research & Innovation Programme Manager
Hesta Health —London
- £40,000 - £50,000 a year
- Temporary
- Hybrid work
- Supervising experience
- Project management
- Bachelor's degree
- Flexible schedule
Quick apply
AI Agent Operations Specialist (FTE 60%)
Delfa AI —London
- APIs
- AI
Quick apply
Clinical Guidelines Assistant
RCPCH —London
- £32,477 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Technical Program Manager, Human Research Lab Operations
Google —London
- Bachelor's degree
Agile Research Delivery Team Administrator B4
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Full-time
- IT
9d
Manager, Client Engagement
ICON Plc —Reading
- Full-time
- Remote
- Marketing
- Business development
- Bachelor's degree
- Employee assistance programme
Project Manager
University of Surrey —Guildford
- £18,847 - £23,025 a year
- Part-time
- Hybrid work
- Project management
- University
- AI
- Relocation assistance
9d
Site Enrollment and Engagement Lead
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
4d
Project Manager
MEDIDATA —London
- Hybrid work
- Microsoft Office
- Project management
- Travel
- Annual leave
Director Clinical Operations, Clinical Project Managers
IQVIA —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
11d
Project Manager, Clinical Trials
Cogstate —London
- £55,000 - £60,000 a year
- Remote
- Computer Science
- Engineering
- Master's degree
- Annual leave
Quick apply
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme

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research operations occupations jobs near middlesex, gtl

Study Owner, eClinical Services

TransPerfect -
London

Quick apply

Job details

Full-time

Qualifications

English
Bachelor's degree
Communication skills

Full job description

Position Summary:

The Study Owner (SO) forms part of the Client Services team within TransPerfect´s Trial Interactive division, working on behalf of clients as an extension to their study team. The Study Owner ensures a complete, contemporaneous and accurate Trial Master File (TMF) and electronic TMF (eTMF) across our clients’ clinical programs. Working with client study teams and functional leads, they assume a key role in the management of a study with a focus on study start up and the TMF with the goal of supporting inspection readiness.

Position responsibilities:

Participate in client Study Owner engagements and consistently deliver quality customer success
Own and account for the TMF on behalf of our clients, across multiple studies and programs
Support inspection readiness as a culture, and compliance with Good Clinical Practices (GCP) regulatory requirements
Assist study teams with all study start up activities utilizing Study Start Up, Clinical Trial Management Systems (CTMS) and eTMF systems
Assist study teams with all maintenance and close out activities utilizing systems such as, but not limited to, CTMS and eTMF systems
Create study-specific TMF Plans on behalf of clients
Help ensure TMF plan compliance
Ensure compliance with client Standard Operating Procedures (SOPs) and work instructions
Meet with study teams to understand events/activities that would impact the TMF
eTMF ongoing user management
May be responsible for creation and or maintenance of events/placeholders or equivalent in the eTMF
Resolve outstanding TMF queries on behalf of clients
Complete periodic TMF quality reviews, at agreed intervals, and ensure documentation is present/complete in the TMF
Identify and report to study leads on TMF trending issues/concerns, determining resolutions and course of actions
Identify continuous improvement opportunities to enhance TMF operational efficiencies
Monitor and assess the overall health of the TMF
Storyboard creation and maintenance to assist with inspection readiness
Support Audits/Inspections as needed
Complete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor

Essential skills required:

Superior written and spoken communication skills in English (written and verbal)
Strong presentation skills
Ability to effectively multitask in order to simultaneously execute multiple projects
Proactive and able to work on own initiative
Exceptional problem-solving/critical thinking skills
Detail-orientated and well organized

Required experience and qualifications:

Bachelor´s degree or equivalent
3 years+ of experience in the Life Sciences industry (pharmaceutical, biotechnology or CRO experience preferred)
Document management/TMF related industry experience in order to have a thorough understanding of the processes associated with the conduct of clinical trials and document management operations
International Council for Harmonization (ICH)/GCP knowledge and understanding
Experience working with eTMF or other eClinical systems such as Veeva Vault or Wingspan IQVIA TMF

Desired skills and experience:

Good interpersonal skills
Ability to build relationships with clients and co-workers
Knowledge of additional languages at professional working proficiency

Quick apply

Refine Your Search

research operations occupations jobs in middlesex, gtl

Study Owner, eClinical Services

Research and insights manager

Research Support Officer

Study Research Assistant

Research Coordinator (PAFTOL Project)

Senior Research Operations Coordinator

Translational Study Coordinator

Research & Innovation Programme Manager

AI Agent Operations Specialist (FTE 60%)

Clinical Guidelines Assistant

Technical Program Manager, Human Research Lab Operations

Agile Research Delivery Team Administrator B4

Manager, Client Engagement

Project Manager

Site Enrollment and Engagement Lead

Clinical Research Coordinator

Project Manager

Director Clinical Operations, Clinical Project Managers

Project Manager, Clinical Trials

Clinical Research Associate - 12 months' monitoring experience required

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