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Jobs at Iqvia in United Kingdom

Scientific Writer – Clinical Pharmacology & Pharmacometrics

IQVIA

England
On-site
GBP 35,000 - 50,000
7 days ago
Be an early applicant
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Hybrid Clinical Pharmacist - Career Growth

IQVIA

East Midlands
Hybrid
GBP 40,000 - 60,000
7 days ago
Be an early applicant

Clinical Pharmacist

IQVIA

East Midlands
Hybrid
GBP 40,000 - 60,000
7 days ago
Be an early applicant

Hybrid Clinical Pharmacist - Career Growth

IQVIA

Peterborough
Hybrid
GBP 40,000 - 50,000
7 days ago
Be an early applicant

Clinical Pharmacist

IQVIA

Peterborough
Hybrid
GBP 40,000 - 50,000
7 days ago
Be an early applicant
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Clinical Pharmacist – Primary Care (Hybrid) & Growth

IQVIA Ltd. (GB80)

East Midlands
Hybrid
GBP 45,000 - 60,000
8 days ago

Clinical Pharmacist

IQVIA Ltd. (GB80)

East Midlands
Hybrid
GBP 45,000 - 60,000
8 days ago

Global CDM Lead: Data Strategy & Delivery

QUK IQVIA Ltd.

England
On-site
GBP 55,000 - 70,000
8 days ago
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Clinical Data Management Lead

QUK IQVIA Ltd.

England
On-site
GBP 55,000 - 70,000
8 days ago

Consultant Cardiologist

IQVIA

Leeds
Hybrid
GBP 200,000 +
8 days ago

Paediatric Echocardiologist – Flexible Bank Roles

IQVIA

Leeds
Hybrid
GBP 200,000 +
8 days ago

Consultant Cardiologist

IQVIA

Warrington
Hybrid
GBP 80,000 - 120,000
8 days ago

Paediatric Echocardiologist – Flexible Bank Roles

IQVIA

Warrington
Hybrid
GBP 80,000 - 120,000
8 days ago

Consultant Cardiologist

IQVIA

Wolverhampton
Remote
GBP 70,000 - 90,000
8 days ago

Paediatric Echocardiologist – Flexible Bank Roles

IQVIA

Wolverhampton
Remote
GBP 70,000 - 90,000
8 days ago

Study Start Up Specialist (UK, homebased), IQVIA Biotech

IQVIA

Stafford
Remote
GBP 40,000 - 60,000
8 days ago

UK Study Start-Up Specialist – Homebased

IQVIA

Stafford
Remote
GBP 40,000 - 60,000
8 days ago

Paediatric Echocardiologist – Flexible Bank Roles

IQVIA

Manchester
Hybrid
GBP 80,000 - 120,000
8 days ago

Consultant Cardiologist

IQVIA

Manchester
Hybrid
GBP 80,000 - 120,000
8 days ago

Consultant Cardiologist

IQVIA

Liverpool
Hybrid
GBP 200,000 +
8 days ago

Paediatric Echocardiography Consultant - Flexible Bank Shifts

IQVIA

Liverpool
Hybrid
GBP 200,000 +
8 days ago

Data Management Team Lead — Strategy, Mentorship & Delivery

QUK IQVIA Ltd.

England
On-site
GBP 60,000 - 80,000
8 days ago

Senior Data Team Lead

QUK IQVIA Ltd.

England
On-site
GBP 60,000 - 80,000
8 days ago

Nursing IPPI Program Lead for Clinical Trials

IQVIA

Reading
On-site
GBP 40,000 - 60,000
8 days ago

Program Delivery Management - Nursing

IQVIA

Reading
On-site
GBP 40,000 - 60,000
8 days ago

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Scientific Writer – Clinical Pharmacology & Pharmacometrics
IQVIA
England
On-site
GBP 35,000 - 50,000
Full time
7 days ago
Be an early applicant

Job summary

A leading global clinical research provider in the United Kingdom is seeking a professional to coordinate the support for uploading CPP documents, prepare and review submissions, and provide scientific writing support. The ideal candidate will have a Bachelor’s degree in health sciences or related fields and experience in scientific writing. Strong organizational skills and proficiency in Word are essential. Join us in improving patient outcomes through innovative treatments.

Qualifications

  • Bachelor’s degree in health sciences, life sciences, or related field.
  • Industry experience in scientific writing and document QC.
  • Proficiency in Word templates and document formatting.

Responsibilities

  • Coordinate support for uploading CPP documents into regulatory systems.
  • Prepare and review CPP documents for submission.
  • Provide scientific writing support for memos and reports.
  • Implement and refine QC processes for CPP documentation.
  • Collaborate with CPP leaders and cross-functional teams.

Skills

Scientific writing
Document quality control
Project management
Attention to detail
Communication skills (English)

Education

Bachelor’s degree in health sciences or related field

Tools

Microsoft Word
Job description
Key Responsibilities
  • Coordinate centralized support for uploading CPP documents (e.g., population PK/PD data transfer plans, analysis plans, and reports) into regulatory systems in compliance with global procedures.
  • Prepare and review CPP documents for submission, ensuring accuracy, consistency, and inspection readiness.
  • Provide scientific writing support for memos, reports, and health authority responses.
  • Implement and refine QC processes for CPP documentation, including maintaining QC checklists and tracking comment resolution.
  • Collaborate with CPP leaders and cross-functional teams to ensure timely delivery of high-quality documents.
  • Support development of templates for CPP reporting, analysis plans, and data transfer plans.
  • Maintain central planning and tracking of CPP document deliverables and timelines.
Education & Experience Requirements
  • Bachelor’s degree in health sciences, life sciences, or related field.
  • Industry experience in scientific writing and document QC.
  • Proficiency in Word templates and document formatting.
  • Strong organizational and project management skills.
  • Excellent written and verbal communication skills in English.
  • Familiarity with population PK/PD report writing and review preferred.

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

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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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