Research operations occupations Work, Jobs in Hartfield, Esx (with Salaries)

Clinical Research Associate
IQVIA —Brighton
- No degree
- Travel
Clinical Research Nurse/Coordinator
Surrey and Sussex Healthcare NHS Trust —Redhill
- £39,959 - £48,117 a year
- Full-time
- Organisational skills
- Communication skills
5d
Technician - Clinical Trials
The Royal Marsden NHS Foundation Trust —Sutton
- £33,262 - £36,027 a year
- Full-time
13d
Applied Research Manager DEMEA
Berry Gardens Limited —Maidstone
- Spanish
- English
- Master's degree
Quick apply
Head of Clinical Research Performance
The Royal Marsden NHS Foundation Trust —Sutton
- £85,641 - £97,746 a year
- Full-time
- Project management
10h
Clinical Trials Programme Manager
ICR —Sutton
- From £50,825 a year
- Call to connect
- Hybrid work
- Laboratory experience
- No degree
8d
Senior Haemato-Oncology Clinical Research Nurse
East Sussex Healthcare NHS Trust —Eastbourne
- £49,387 - £56,515 a year
- Full-time
- Leadership
- Communication skills
- Employee assistance programme
5d
Sussex Commercial Research Delivery Centre (CRDC) Agile Research Nurse
University Hospitals Sussex NHS Foundation Trust —Brighton
- £39,959 - £48,117 a year
- Full-time
- Driving
- Communication skills
- Nursing
8d

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research operations occupations jobs near hartfield, esx

Clinical Research Associate

IQVIA -
Brighton

Apply Now

Job details

Qualifications

Project implementation

Full job description

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK

Apply today and forge a career with greater purpose, make an impact and never stop learning!

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.

Apply Now

Refine Your Search

research operations occupations jobs in hartfield, esx

Clinical Research Associate

Clinical Research Nurse/Coordinator

Technician - Clinical Trials

Applied Research Manager DEMEA

Head of Clinical Research Performance

Clinical Trials Programme Manager

Senior Haemato-Oncology Clinical Research Nurse

Sussex Commercial Research Delivery Centre (CRDC) Agile Research Nurse

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