Global Project Manager - EU - Immunology/Oncology at ICON
Remote, Scotland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

04 Sep, 25

Salary

0.0

Posted On

05 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Risk, Cultural Awareness, Presentation Skills, Clinical Development, Clinical Research, Communication Skills, Strategic Thinking, Oncology, Critical Thinking, Analytical Skills, Interpersonal Skills, Neurology

Industry

Pharmaceuticals

Description

New opportubity for an experience Senior Global Clinical Project Manager to join our growing FSP program sponsor dedicated. This is a permanent and home-based role.

Responsibilities

THE ROLE

  • Accountable for the delivery and quality of site level activities in Phase I-IIIb Clinical Development studies; act as link between Clinical Site Leads, Global functions & CRO counterparts - single point of contact for site management & operational topics/escalations; support information channelling and issue resolution for the studyProvide leadership, strategic direction and operational oversight for Clinical Site Lead (CSL) activities across assigned study(ies) in response to quality and performance oversight measures and trends
  • Serve as the operational delivery expert for the study(ies) and promote data-driven, realistic planning at the site and study level. Drive delivery-focussed accountability and ownership amongst key external (CRO/vendor partners) and internal partners as appropriate
  • Facilitate identification and implementation of operational excellence strategies within studies - leveraging expertise within Global Development Operations (GDO) and other partner functions
  • Ensure timely and appropriate escalation of trends, issues and risks within the Clinical Operations Team/Clinical Trial Team/CRO/Vendor Team, department Leadership Team and/or Senior Management as appropriate
  • Promote solution-orientated thinking and issue resolution at the country and study team level. Provide an escalation pathway to ensure study-specific major observations from CSLs are relayed to and followed up by the appropriate internal and/or external business partners
  • Support product and study-specific onboarding for new CDPC team members and contribute to enhancing their site/study management capabilities/skills
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