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2,395

Clinical Research jobs in United Kingdom

Experienced Senior CRA - Oncology - Phase IIb-III

Experienced Senior CRA - Oncology - Phase IIb-III
ICON Strategic Solutions
United Kingdom
GBP 60,000 - 80,000
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Experienced Senior CRA - Oncology - Phase IIb-III

Experienced Senior CRA - Oncology - Phase IIb-III
ICON plc
United Kingdom
GBP 50,000 - 70,000

Locum consultant Obstetrician & Gynaecologist

Locum consultant Obstetrician & Gynaecologist
Barts Health NHS Trust
London
GBP 80,000 - 120,000

contentmarketing.ai - Trial Manager (remote UK)

contentmarketing.ai - Trial Manager (remote UK)
Brafton Inc.
United Kingdom
Remote
GBP 30,000

Head of Medical Oncology

Head of Medical Oncology
VCA Inc.
United Kingdom
GBP 60,000 - 100,000
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Business Development Director (Clinical Trials)

Business Development Director (Clinical Trials)
Clinigen
United Kingdom
GBP 80,000 - 120,000

Consultant in Ophthalmology - Glaucoma

Consultant in Ophthalmology - Glaucoma
Integrated Care System
Peterborough
GBP 80,000 - 130,000

Senior Product Manager - 12 Month Fixed Term

Senior Product Manager - 12 Month Fixed Term
NEOM Wellbeing
London
GBP 200,000 +
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Registered Nurse, Homecare - Generous Sign On Bonus!

Registered Nurse, Homecare - Generous Sign On Bonus!
Care New England Health System
Warwick
USD 60,000 - 80,000

Remote Senior Frontend Developer (m/w/d) - Vaadin/ GWT (Google Web Toolkit)/Apache Wicket

Remote Senior Frontend Developer (m/w/d) - Vaadin/ GWT (Google Web Toolkit)/Apache Wicket
IQVIA
London
Remote
GBP 55,000 - 75,000

Consultant Medical Oncologist

Consultant Medical Oncologist
NHS Scotland
Dundee
GBP 80,000 - 110,000

Experienced Senior CRA - Oncology - Phase IIb-III

Experienced Senior CRA - Oncology - Phase IIb-III
Pharmaceutical Research Associates, Inc
United Kingdom
GBP 50,000 - 70,000

Strategic Communications Writer – Pharma Review

Strategic Communications Writer – Pharma Review
IQVIA Ltd. (GB80)
London
GBP 40,000 - 60,000

Specialist grade Psychiatrist in General Adult Psychiatry

Specialist grade Psychiatrist in General Adult Psychiatry
Integrated Care System
Crawley
GBP 80,000 - 100,000

Presentation Design Manager

Presentation Design Manager
IQVIA
London
USD 40,000 - 65,000

Presentation Design Manager

Presentation Design Manager
QUK IQVIA Ltd.
London
GBP 35,000 - 50,000

Consultant in General Adult Psychiatry Community CMHT

Consultant in General Adult Psychiatry Community CMHT
Integrated Care System
Bury
GBP 70,000 - 100,000

Consultant in Rehabilitation Medicine: Community Rehabilitation

Consultant in Rehabilitation Medicine: Community Rehabilitation
Integrated Care System
Plymouth
GBP 76,000 - 104,000

Consultant Psychiatrist within Community Mental Health Service

Consultant Psychiatrist within Community Mental Health Service
Integrated Care System
Plymouth
GBP 70,000 - 100,000

Clinical Photography Lead

Clinical Photography Lead
The Royal Wolverhampton NHS Trust
Dudley
GBP 35,000 - 45,000

CK216107 - Consultant Gastroenterologist (Advanced Endoscopy)

CK216107 - Consultant Gastroenterologist (Advanced Endoscopy)
NHS Scotland
Aberdeen City
GBP 80,000 - 120,000

Clinical Photography Lead

Clinical Photography Lead
Integrated Care System
Dudley
GBP 35,000 - 50,000

Process Automation Manager

Process Automation Manager
Eucalyptus
London
GBP 60,000 - 85,000

Automation Manager

Automation Manager
Eucalyptus
London
GBP 70,000 - 100,000

Business Process Automation Manager

Business Process Automation Manager
Eucalyptus
London
GBP 70,000 - 100,000

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Experienced Senior CRA - Oncology - Phase IIb-III

ICON Strategic Solutions
United Kingdom
GBP 60,000 - 80,000
Job description

As an experienced Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

  • May serve as Lead CRA for specific study providing study level oversight and support for CRA's assigned to the study.
  • This assignment ensure study level information is shared with assigned CRA's and has key role in establishing site monitoring strategy for study.
  • Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
  • Responsible for the implementation of risk based monitoring approaches at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
  • Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
  • Responsible in close collaboration with study team for the activities during site activation phase to speed up the process and activate the site in the shortest possible timeframe.
  • Ensure site compliance with study protocol, ICH-GCP, and local/country regulations.
  • Ensure ongoing adequacy of site (facilities, staff) for trial conduct.
  • Ensure source and other site documentation is adequate and in compliance with ALCOA-CCEA
  • Involved with site level recruitment strategy and prioritization and implementation in partnership with other functional areas.
  • Ensures site non-IMP study supplies are adequate for trial conduct.
  • Ensures that clinical drug supplies are appropriately used, handled, and stored and returns are accurately inventoried and detailed.
  • Oversees the appropriate destruction of clinical supplies.
  • Ensures site staff complete data entry and resolve queries within expected timelines.
  • Ensures validity and completeness of data collected at trial sites.
  • Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs) are reported within the required reporting timelines and documented as appropriate.
  • Maintains complete, accurate and timely data and essential documents in relevant systems used for trial management.
  • Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs. Promptly communicates relevant status information and issues to appropriate stakeholders.
  • Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
  • Aligns with relevant training requirements. Act as local expert in assigned protocols. Develops therapeutic knowledge sufficient to support role and responsibilities.
  • Works closely with CTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and for quality issues identified at the site during routine monitoring visits.
  • Prepares trial sites for close out, conduct final close out visit.
  • Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff.
  • May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate.
  • May be responsible for up to 10 sites across 2-4 protocols, dependent on complexity of protocols and site activity. Responsible for managing own travel budget within provided guidelines.


Senior CRA: 5 years of experience minimum
  • May serve as Lead CRA for specific study providing study level oversight and support for CRA's assigned to the study.
  • This assignment ensure study level information is shared with assigned CRA's and has key role in establishing site monitoring strategy for study.
  • Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
  • Responsible for the implementation of risk based monitoring approaches at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
  • Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
  • Responsible in close collaboration with study team for the activities during site activation phase to speed up the process and activate the site in the shortest possible timeframe.
  • Ensure site compliance with study protocol, ICH-GCP, and local/country regulations.
  • Ensure ongoing adequacy of site (facilities, staff) for trial conduct.
  • Ensure source and other site documentation is adequate and in compliance with ALCOA-CCEA
  • Involved with site level recruitment strategy and prioritization and implementation in partnership with other functional areas.
  • Ensures site non-IMP study supplies are adequate for trial conduct.
  • Ensures that clinical drug supplies are appropriately used, handled, and stored and returns are accurately inventoried and detailed.
  • Oversees the appropriate destruction of clinical supplies.
  • Ensures site staff complete data entry and resolve queries within expected timelines.
  • Ensures validity and completeness of data collected at trial sites.
  • Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs) are reported within the required reporting timelines and documented as appropriate.
  • Maintains complete, accurate and timely data and essential documents in relevant systems used for trial management.
  • Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs. Promptly communicates relevant status information and issues to appropriate stakeholders.
  • Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
  • Aligns with relevant training requirements. Act as local expert in assigned protocols. Develops therapeutic knowledge sufficient to support role and responsibilities.
  • Works closely with CTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and for quality issues identified at the site during routine monitoring visits.
  • Prepares trial sites for close out, conduct final close out visit.
  • Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff.
  • May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate.
  • May be responsible for up to 10 sites across 2-4 protocols, dependent on complexity of protocols and site activity. Responsible for managing own travel budget within provided guidelines.

Experience required:

• BA/BS degree with ≥5years of experience in pharmaceutical related drug development or direct equivalent experience.

• Five years site monitoring and/or site management experience.

• A minimum of 2 years of Oncology, Ophthalmology, and/or Gene Therapy or other directly relevant therapeutic area experience.

• Strong working knowledge of GCP, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.

• Strong critical thinking and problem solving skills.

• Strong IT skills in appropriate software and company systems.

• Willingness to travel up to 40% with overnight stay away from home.

• Proficient in speaking and writing English.

• Good written and oral communication.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others


Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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