Clinical research specialist Work, Jobs in Send, Sry (with Salaries)

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
- From £58,500 a year
- English
- Microsoft Office
- Bachelor's degree
Research Administrator
Great Ormond Street Hospital for Children —London
- £34,186 - £37,389 a year
- Part-time
- Computer literacy
- Administrative experience
- Organisational skills
6d
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
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Clinical Evaluation Specialist - Radiology
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
6d
Occupational Inclusion Specialist
The Fedcap Group —Guildford
- £33,048 - £35,535 a year
- Full-time
- Travel
- In-person
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Clinical Trial Manager at CCTU
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Travel
- Communication skills
- Time management
- Annual leave
- Employee assistance programme
10d
Senior Clinical Trainer
HCRG Care Group —Guildford
- £39,959 - £48,117 a year
- Supervising experience
- Project management
- Education
- Employee discount
Quick apply
7d
AI Health Technology Research Specialist
Veiksme Tech Limited —Ashford
- £45,000 - £55,000 a year
- Full-time
- Hybrid work
- Doctoral degree
- Communication skills
Quick apply
10d
Senior Clinical Scientist (Magnetic Resonance Physics)
University College London Hospitals NHS Foundation Trust —London
- £66,274 - £73,496 a year
- Full-time
- University
- Leadership
- Communication skills
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Specialty Doctor
Change Grow Live —West Sussex
- £92,575.07 - £103,849.41 a year
- Remote
- Travel
- IT
- Communication skills
- Annual leave
- Employee assistance programme
10d
Chief Clinical Physiologist – Arrhythmia Specialist
Great Ormond Street Hospital for Children —London
- £58,133 - £65,261 a year
- Full-time
- Master's degree
- Bachelor's degree
- Organisational skills
4d
Site Start-Up Specialist
Fortrea —Maidenhead
- Full-time
- Hybrid work
- Microsoft Office
- Communication skills
Data Manager -B4
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Full-time
- Administrative experience
- IT
- Medical terminology
4d
Science Education & Innovation Lead
Tropic Skincare —Croydon
- From £70,000 a year
- Hybrid work
- Doctoral degree
- Communication skills
- Employee assistance programme
- Employee discount
Quick apply
Medicine Specialist (Fluent in German) - Freelance AI Trainer Project
Meridial —London
- £8 - £65 an hour
- Remote
- Doctoral degree
- Engineering
- Master's degree
- Annual leave
Research GP
Healthcare Central London —London
- Part-time
- Hybrid work
- IT
- Leadership
- Communication skills
- Employee assistance programme
Quick apply
12d
Clinical Scientist/Clinical Scientist - Graduate Trainee
NHS Blood and Transplant —Tooting
- £39,959 - £56,515 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee assistance programme
16h

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Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

IQVIA -
Reading

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Job details

From £58,500 a year

Qualifications

Clinical research
Project coordination
English
Microsoft Office
Bachelor's degree
Communication skills

Full job description

The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials.

Senior Clinical Project Support Specialist will provide operational support and coordination for global clinical trials, ensuring efficient trial execution from planning through close-out. Responsible for managing trial-related documentation, systems, communication, and logistics in compliance with SOPs, ICH-GCP, and regulatory requirements, while meeting quality and timeline objectives.

Main Responsibilities

Plan, coordinate, and execute clinical trial activities across regions in compliance with ICH-GCP, ensuring timely and high-quality delivery.
Maintain and oversee trial documentation (e.g., ISF, TMF, submissions), ensuring completeness, accuracy, timeliness and audit readiness.
Collaborate with global and regional stakeholders, vendors, and trial teams to ensure seamless trial conduct and communication.
Manage and maintain clinical trial systems, databases, and tracking tools ensuring data accuracy.
Prepare and distribute project plans, status updates, reports, and presentation materials.
Monitor trial progress, budgets, and system data, identifying risks and implementing corrective actions as needed.
Coordinate documentation workflows, regulatory submissions, and communication with authorities and regional teams.
Support reporting, trial close-out activities, and preparation of key deliverables (e.g., CTR appendices).
Coordinate logistics for trial meetings, materials, and supplies.
Contribute to quality oversight, inspection readiness, and best practices in clinical trial conduct.
Act as a key point of contact for trial-related systems, documentation, and operational queries.

Required Skills and Qualifications

University degree qualified and/or comparable professional education.

At least 5 years’ experience in clinical trial operations or project coordination including solid background in vendor management.

Experience in global clinical trials.

Fluent in written and spoken English.

Exceptional communication and stakeholder management skills.

Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Excellent organizational and problem-solving skills with ability to work independently, prioritize tasks, and manage projects in a complex international environment.

Detail-oriented with strong commitment to quality and compliance.

Proficiency in MS Office and clinical trial systems/tools. Knowledge of OMP / Veeva system will be highly advantageous.

For candidates based in Austria, we offer a market-competitive gross annual salary starting at €58,500, depending on your qualifications and relevant professional experience.

Please apply with your English CV.

Please note this role is not eligible for the UK visa sponsorship.

Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical research specialist jobs in send, sry

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

Research Administrator

Clinical Research Fellow

Clinical Evaluation Specialist

Clinical Evaluation Specialist - Radiology

Clinical Research Scientist

Occupational Inclusion Specialist

Clinical Trial Manager at CCTU

Senior Clinical Trainer

AI Health Technology Research Specialist

Senior Clinical Scientist (Magnetic Resonance Physics)

Specialist, R&D Contracts & Business Operations

Specialty Doctor

Chief Clinical Physiologist – Arrhythmia Specialist

Site Start-Up Specialist

Data Manager -B4

Science Education & Innovation Lead

Medicine Specialist (Fluent in German) - Freelance AI Trainer Project

Research GP

Clinical Scientist/Clinical Scientist - Graduate Trainee

I want to receive the latest job alerts for clinical research specialist in send, sry

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