Clinical trial manager Work, Jobs in Oxford, Oxf (with Salaries)

Site Activation Specialist
IQVIA —Reading
- Full-time
- Remote
- Travel
- Work from home
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- Project management
- Team management
- Annual leave
Clinical Operations Manager
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Full-time
- Organisational skills
- Communication skills
Clinical Study Manager (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- Leadership
Quick apply
13h
Clinical Trials Administrator with Play
University of Oxford —Oxford
- £28,437 - £34,732 a year
- Full-time
- In-person
- Communication skills
12d
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Clinical Specialist
AtriCure International —Oxford
- Microsoft Powerpoint
- Up to 50% travel
- Bachelor's degree
- Annual leave
Data Team Lead
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Leadership
- Work from home
6d
Connected Devices - Primary analyst, Spirometry
IQVIA —Reading
- Full-time
- Remote
- Computer literacy
- Mentoring
- Computer skills
- Work from home
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Computer literacy
- Travel
- Computer skills
Senior Medical Writer (remote US-based)
Porterhouse Medical Group —Reading
- Remote
- Management
- Doctoral degree
- Master's degree
- Annual leave
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
- Work from home
Senior Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
NIHR SPCR Nursing Commercial Research Fellow
University of Oxford —Oxford
- £49,119 - £74,896 a year
- Part-time
- Research
- University
- Leadership
14d
Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)
IQVIA —Reading
- Full-time
- Remote
- English
- Databases
- Mentoring
- Work from home
Specialist Biomedical Scientist (x2)
Deciphex —Oxford
- 8 hour shift
- Laboratory experience
- Mentoring
- Annual leave
Quick apply
Sr. Manager, Site Budgets and Contracts
Moderna, Inc. —Oxford
- Full-time
- Travel
- Annual leave
12d
Senior Medical Writer
IQVIA —Reading
- Full-time
- Remote
- Doctoral degree
- Computer literacy
- Master's degree
- Work from home
Senior Clinical Researcher in Primary Care Clinical Trials, Infectious Diseases and Pandemic Preparedness
University of Oxford —Oxford
- £85,732 - £111,133 a year
- Full-time
- Doctoral degree
- Organisational skills
- Leadership
6d
Sample Management Technician
University of Oxford —Oxford
- £28,437 - £34,732 a year
- Weekend availability
- Travel
- Communication skills
19h

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Site Activation Specialist

IQVIA -
Reading

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Document control
Clinical research
Project schedule tracking
Multidisciplinary collaboration
Project progress tracking
Progress tracking

Full job description

Reading, United Kingdom | Full time | Home-based | R1554279

Business Unit: Global Site Activation

Location: UK, homebased, occasional travel to Reading office (monthly)

Make an impact on patient health!

IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.

We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.

IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.

We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

Job Overview:

You will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary
Review documents for completeness, consistency, and accuracy, under guidance of senior staff
Prepare site documents and inform team members of the completion of regulatory contractual documents
Distribute completed documents to sites and internal project team members
Update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information
Review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents

Requirements:

Experience of site activation activities including but not limited to regulatory submissions, site feasibility, site documentation (questionnaires, CDAs, regulatory, ethics, Informed Consent Forms and Investigator Packs), and negotiating contracts and budgets with sites
3 years’ minimum previous experience supporting clinical trials in a healthcare environment is required.

Join IQVIA and let’s create a healthier world together:

Exposure across 21 Therapeutic Areas
Be part of a global team who operate across 141 locations
Exposure across a variety of studies and projects
Access to new, innovative technologies
Work within a collaborative and vibrant environment
Own your career!

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical trial manager jobs in oxford, oxf

Site Activation Specialist

Trial Manager

Clinical Operations Manager

Clinical Study Manager (Medical Devices)

Clinical Trials Administrator with Play

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Clinical Specialist

Data Team Lead

Connected Devices - Primary analyst, Spirometry

Senior Quality Assurance Manager (Clinical)

Senior Medical Writer (remote US-based)

Senior Clinical Technology Specialist

Senior Coordinator

NIHR SPCR Nursing Commercial Research Fellow

Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)

Specialist Biomedical Scientist (x2)

Sr. Manager, Site Budgets and Contracts

Senior Medical Writer

Senior Clinical Researcher in Primary Care Clinical Trials, Infectious Diseases and Pandemic Preparedness

Sample Management Technician

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