Global Study Manager, Gene & Cardiovascular Therapies

KCR Placement; Reading; On-site; GBP 70,000 - 110,000; Full time

Job summary

ICON Strategic Solutions is seeking a Global Study Manager to support the delivery of Cell Therapy global clinical studies from protocol development through close-out and archiving. Working in a cross-functional global study team, you will collaborate with internal stakeholders, CROs, and external vendors to ensure studies are delivered on time, within budget, and to the highest quality and compliance standards.

Ambitious cardiovascular programmes may be included.

Qualifications

• Degree qualified in Life Sciences, Medical Sciences, Biological Sciences, or related field.
• 3+ years of experience in clinical research, pharmaceutical development, biotechnology, or a CRO environment.
• Strong understanding of clinical development and the drug development process.
• Excellent knowledge of ICH-GCP and global clinical trial regulations.
• Proven project management and organisational skills.
• Strong stakeholder management and communication skills.
• Experience working effectively within global, cross-functional teams.
• Previous experience supporting cardiovascular clinical trials is highly desirable.
• Proactive, collaborative, and able to work independently in a fast-paced environment.

Responsibilities

• Support delivery of Cell Therapy global clinical studies from protocol development through study close-out.
• Collaborate with internal stakeholders, CROs and vendors to ensure on-time, on-budget study delivery.
• Ensure high-quality and regulatory-compliant study conduct across global teams.

Skills

Project management

Stakeholder management

Global cross-functional collaboration

ICH-GCP knowledge

Communication skills

Cardiovascular trials experience

Education

Life Sciences degree

Job description

ICON Strategic Solutions is seeking a Global Study Manager to support the delivery of Cell Therapy global clinical studies from protocol development through close-out and archiving. Working in a cross-functional global study team, you will collaborate with internal stakeholders, CROs, and external vendors to ensure studies are delivered on time, within budget, and to the highest quality and compliance standards.

Ambitious cardiovascular programmes may be included.