Country Clinical Project Lead – Oncology/Respiratory

IQVIA Holdings Inc.

Reading

On-site

GBP 55,000 - 76,000

Full time

14 days+

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Job summary

IQVIA Holdings Inc. is seeking a Clinical Project Manager to lead study commitments at the country level in Reading, UK.

You will oversee a Local Study Team of CRAs and CSAs, ensure quality data delivery, and manage regulatory submissions with EC/IRB and authorities. You will coordinate site selection, feasibility assessments, and budgets, while maintaining country-level master documentation and CTMS setup.

Qualifications

  • Bachelor degree in life sciences or related field.
  • Minimum 1 year of local Clinical Project Management experience.
  • Strong knowledge of Oncology or Respiratory therapeutic areas.
  • Proven ability to lead cross-functional teams to deliver trials on time, budget and quality.
  • Excellent spoken and written English.

Responsibilities

  • Oversee country study commitments and timely data delivery to required quality.
  • Lead Local Study Team (CRA/CSA) for assigned studies.
  • Coordinate site selection, site risk assessment and site qualification visits.
  • Ensure timely regulatory submissions to EC/IRB and regulatory authorities.
  • Prepare country Master CSA and MICF and translations.
  • Set up CTMS and local websites as required by local laws.
  • Oversee monitoring activities from site activation to study closure.
  • Identify risks and resolve complex study issues.
  • Organise regular Local Study Team meetings.
  • Travel nationally and internationally as required.

Skills

Leadership
Cross-functional teamwork
Project management
Negotiation
Attention to detail
English language
IT systems
Travel

Education

Bachelor's degree in life science or related field

Tools

CTMS
Clinical financial system

Job description

IQVIA Holdings Inc. is seeking a Clinical Project Manager to lead study commitments at the country level in Reading, UK.

You will oversee a Local Study Team of CRAs and CSAs, ensure quality data delivery, and manage regulatory submissions with EC/IRB and authorities. You will coordinate site selection, feasibility assessments, and budgets, while maintaining country-level master documentation and CTMS setup.

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