Clinical office coordinator, neuroscience, stroke and palliative care Work, Jobs in Bracknell, Brk (with Salaries)

Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
8d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
CHC Clinical Assessor
Central London Community Healthcare NHS Trust —Wembley
- £45,953 - £54,254 a year
- Full-time
- Rehabilitation centre
- Care plans
1d
Clinical Office Coordinator, Trauma & Orthopaedics
Ashford and St. Peter's Hospitals NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Customer service
- Communication skills
- Employee discount
2h
Patient Pathway Coordinator, Neuroscience, Stroke and Palliative Care
Ashford and St. Peter's Hospitals NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Organisational skills
- Communication skills
- Employee discount
8d
Medical Secretary – Oncology
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Full-time
- Microsoft Powerpoint
- Customer service
- Patient care
- Annual leave
2d
Research Assistant in Brain Vascular Epigenomics – UK Dementia Research Institute
Imperial College London —White City
- £43,863 - £47,223 a year
- Full-time
- C++
- University
- Linux
4d
Macmillan Clinical Nurse Specialist, Palliative Care
London North West University Healthcare NHS Trust —London
- £55,524 - £62,652 a year
- Full-time
- Hospice
1d
Learning Disability Clinical Assessor
Central London Community Healthcare NHS Trust —Wembley
- £45,953 - £54,254 a year
- Full-time
- Rehabilitation centre
3d
CRA II
Fortrea —Maidenhead
- Full-time
- Communication skills
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Research Associate in Brain Vascular Epigenomics – UK Dementia Research Institute
Imperial College London —White City
- £50,733 - £59,484 a year
- Full-time
- Microsoft Outlook
- Doctoral degree
- University
7h
Senior Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
Medical Advisor, Neuropsychiatry
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Project management
- Travel
- In-person
Operations Coordinator, Cell and Gene Therapies
UPS —London
- Full-time
- Microsoft Excel
- Heavy lifting
- Communication skills
PCN Care Coordinator
The Confederation, Hillingdon CIC —Hillingdon
- £26,000 - £36,000 a year
- Microsoft Office
- Travel
- Organisational skills
Quick apply
8d
Medical Receptionist/Administrator
Synthesis Clinic —Reading
- £15 - £17 an hour
- Full-time
- Google Suite
- Customer service
- Administrative experience
- Free parking
Quick apply
1d
Children & Young People's Coordinator
The Confederation, Hillingdon CIC —Hillingdon
- £35,000 - £42,000 a year
- Childcare
- Microsoft Excel
- Microsoft Office
Quick apply
9d
Research Technician in Neuroepigenomics
Imperial College London —White City
- £37,108 - £40,166 a year
- Full-time
- Laboratory experience
- University
- Communication skills
- Annual leave
9d
Care Coordinator (Care Home Team)
Procare Health Limited —Hindhead
- £24,785 - £28,500 a year
- Part-time
- Microsoft Office
- Organisational skills
- IT
Quick apply
9d

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clinical office coordinator, neuroscience, stroke and palliative care jobs near bracknell, brk

Clinical Registry Coordinator

ICON Plc -
Reading

Apply Now

Job details

Full-time
8 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Microsoft Office
Project management
Bachelor's degree

Full job description

Clinical Registry Coordinator

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Registry Coordinator at ICON Plc, you will be instrumental in ensuring the transparency and integrity of clinical trial data and results.

What You Will Do:

Key responsibilities include:

Provides clinical registry support, oversight and/or accountability for one or more development programs for clinical trials.
Takes a leadership role with the clinical development team and other internal and external partners to establish, align and confirm clinical registry expectations for assigned trial(s).
Develops and delivers the Disclosure Plan with the CDTL and Patent attorney.
With the CDT and other functional partners: – Gathers content and integration requirements for registration records – Establishes expectations for dataset content and structure. – Set timelines and follow-up regularly to ensure delivery of all clinical trial disclosure milestones.
Responsible for submission of approved documents and content to registries worldwide. . Submissions are made by the Clinical Registry Administrators, either directly such as for clinicaltrials.gov or the EU clinical trial register, or indirectly by providing to the local operating company staff for subsequent submissions to local registries
Responsible for tracking, reporting and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group
Assisting business partners, external partners and local operating companies in maintaining accurate and correct (source) data, relevant to the disclosure process
Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning

Your Profile:

Required qualifications and experience:

A minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO or other clinical development service organization) is required.
Bachelor’s degree in Health or Science discipline with experience in clinical research (typical roles: clinical trial manager, regulatory submissions lead)
Clinical Registry experience preferred
Experience working on a clinical trial or regulatory document management preferred
Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
Project management skills.
Vendor management skills.
Advanced Microsoft Office skills including the ability to manipulate and analyze data

#LI-Remote

#LI-RS1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

Apply Now

Refine Your Search

clinical office coordinator, neuroscience, stroke and palliative care jobs in bracknell, brk

Clinical Registry Coordinator

Clinical Research Associate I

CHC Clinical Assessor

Clinical Office Coordinator, Trauma & Orthopaedics

Patient Pathway Coordinator, Neuroscience, Stroke and Palliative Care

Medical Secretary – Oncology

Research Assistant in Brain Vascular Epigenomics – UK Dementia Research Institute

Macmillan Clinical Nurse Specialist, Palliative Care

Learning Disability Clinical Assessor

CRA II

Sr. Clinical Project Manager (Europe)

Research Associate in Brain Vascular Epigenomics – UK Dementia Research Institute

Senior Coordinator

Medical Advisor, Neuropsychiatry

Operations Coordinator, Cell and Gene Therapies

PCN Care Coordinator

Medical Receptionist/Administrator

Children & Young People's Coordinator

Research Technician in Neuroepigenomics

Care Coordinator (Care Home Team)

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