Clinical associate Work, Jobs in Long Sutton, Ham (with Salaries)

Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
Community Healthcare Assistant - SW Surrey
HCRG Care Group —Guildford
- From £27,674 a year
- Call to connect
- Hybrid work
- Experience working with children
- Training & development
- Communication skills
- Employee discount
Quick apply
10d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Associate Clinical Project Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Leadership
- Work from home
Clinical Trial Supplies Associate ** Farnborough, UK **
サイネオス・ヘルス —Farnborough
- English
- Travel
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
- Recruiting
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Associate Case Processing Manager (Line Management position)
PrimeVigilance —Guildford
- Full-time
- Hybrid work
- Nursing
- Team management
- Quality control
Quick apply
Experienced Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
- Recruiting
10d
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Sales Specialist, Peripheral Vascular Disease - South West & South Wales
BD —Winnersh
- £43,300 - £66,025 a year
- Presentation skills
- Travel
- Organisational skills
13d
Clinical Business Operations Associate - Portfolio & Operations Support
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Analysis skills
- Bachelor's degree
- Work from home
Medical Director - Oncology , Sponsor Dedicated (Home-Based)
IQVIA —Reading
- Full-time
- Remote
- Management
- Sales
- Business development
- Work from home
9d
Experience Patient Services Receptionist Administrator
Farnham Road Practice —Slough
- From £14 an hour
- Full-time
- Computer literacy
- Administrative experience
- Travel
- Free parking
- Store discount
Quick apply
11d
Associate Pharmacovigilance Project Director (Delivery)- Europe
PrimeVigilance —Guildford
- Full-time
- Remote
- Management
- Conflict management
- Leadership
Quick apply
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Safeguarding Care Coordinator ( Maternity Cover )
Andover PCN —Andover
- £13.57 - £15.27 an hour
- Full-time
- Hybrid work
- Microsoft Outlook
- Writing skills
- Research
- Store discount
- Health & wellbeing programme
Quick apply
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- Research
- University
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development

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clinical associate jobs near long sutton, ham

Clinical Research Associate - IQVIA Biotech

IQVIA -
Reading

Apply Now

Job details

Full-time

Qualifications

Clinical research
Stakeholder liaison
Filing
Recruiting
Clinical compliance monitoring
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination
Project progress tracking

Full job description

Reading, United Kingdom | Full time | Field-based | R1521406

At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech tailored delivery model, we accelerate clinical development from early phase through global registrational studies.

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites as required

*Please note - this role is not eligible for visa sponsorship*

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

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

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 associate jobs in long sutton, ham

Clinical Research Associate - IQVIA Biotech

Community Healthcare Assistant - SW Surrey

Clinical Research Associate I

Associate Clinical Project Manager - Sponsor Dedicated

Clinical Trial Supplies Associate Farnborough, UK

Clinical Research Associate II

Senior Clinical Research Associate

Local Study Associate Director

Associate Case Processing Manager (Line Management position)

Experienced Clinical Research Associate

Senior Regulatory Affairs Specialist

Sales Specialist, Peripheral Vascular Disease - South West & South Wales

Clinical Business Operations Associate - Portfolio & Operations Support

Medical Director - Oncology , Sponsor Dedicated (Home-Based)

Experience Patient Services Receptionist Administrator

Associate Pharmacovigilance Project Director (Delivery)- Europe

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Safeguarding Care Coordinator ( Maternity Cover )

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

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

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