Clinical project manager Work, Jobs in Chalgrove, Oxf (with Salaries)

Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Employee assistance programme
10d
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- Project management
- Team management
- Annual leave
13d
ECOA Project Manager
ICON Plc —Reading
- Full-time
- Remote
- Presentation skills
- Bachelor's degree
- Leadership
- Employee assistance programme
11d
Senior Study Startup Specialist
PSI CRO —Oxford
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
Quick apply
Clinical Research Administator
University of Oxford —Oxford
- £32,108 - £40,514 a year
- Full-time
- Oracle
- Administrative experience
- Organisational skills
Change Manager
Siemens Healthineers —Oxford
- Full-time
- Hybrid work
- Continuous improvement
- Communication skills
- Annual leave
3d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Data Team Lead
IQVIA —Reading
- Full-time
- Remote
- Oracle
- Bachelor's degree
- Leadership
- Work from home
3d
Project Manager, IRT
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Leadership
- Employee assistance programme
4d
Principal Investigator
Velocity Clinical Research, Inc. —High Wycombe
- Full-time
- Travel
Quick apply

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clinical project manager jobs near chalgrove, oxf

Clinical Registry Coordinator

ICON Plc -
Reading

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Job details

Full-time
10 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Stakeholder collaboration
Microsoft Office Suite
Project management
Bachelor's degree
Multidisciplinary collaboration
Pharmaceutical industry setting experience

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 project manager jobs in chalgrove, oxf

Clinical Registry Coordinator

Trial Manager

ECOA Project Manager

Senior Study Startup Specialist

Clinical Research Administator

Change Manager

Local Study Associate Director

Senior Clinical Data Manager - sponsor dedicated - oncology

Senior Clinical Programmer I

Data Team Lead

Project Manager, IRT

Principal Investigator

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