Clinical research coordinator Work, Jobs in Stratfield Saye, Ham (with Salaries)

Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
3d
Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
3d
Linguistic Validation & eCOA Team Lead
IQVIA —Reading
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Bachelor's degree
Senior Site Activation Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
13d
Youth Support Worker
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Part-time
- Hospital
- Travel
- Communication skills
9d
Senior Registered Veterinary Nurse - HDU & Wards
IVC —High Wycombe
- Up to £37,500 a year
- Weekend availability
- Leadership
- Nursing
- Annual leave
- Employee discount

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Clinical Registry Coordinator

ICON Plc -
Reading

Apply Now

Job details

Full-time
3 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?

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Refine Your Search

clinical research coordinator jobs in stratfield saye, ham

Clinical Registry Coordinator

Clinical Registry Coordinator - UK Based

Linguistic Validation & eCOA Team Lead

Senior Site Activation Coordinator

Youth Support Worker

Senior Registered Veterinary Nurse - HDU & Wards

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