Global Study Manager - Remote Clinical Trials Lead

Meeveem Limited; Reading; On-site; GBP 65,000 - 95,000; Full time

Benefits offered by this job

Competitive base salary

Health coverage

Retirement and pension plans

Life assurance

Wellbeing resources

Learning and development opportunities

Job summary

ICON is seeking a Global Study Manager to be fully integrated in the FSP clinical operations team and deliver global clinical studies. This permanent, home-based role requires managing study activities, vendors, budgets, and regulatory compliance across regions.

You will contribute to risk management, quality assurance, and documentation while collaborating with internal teams and external partners. Advanced degree is desirable.

Qualifications

• Bachelor’s degree in life sciences or related field and 5+ years in clinical research.
• Experience in global clinical project management and vendor oversight.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Proven ability to deliver projects on time and within budget.
• Experience with internal and external vendors and budgets.

Responsibilities

• Support planning, setup, execution, and close-out of global clinical studies.
• Oversee vendors and country teams to ensure smooth study delivery.
• Collaborate with internal teams and external partners.
• Help develop and update study documents (protocols, consent forms).
• Manage third-party vendors, contracts and budgets; ensure inspection readiness.

Skills

Global study management

Clinical operations

Vendor management

ICH-GCP

Regulatory knowledge

Communication

Problem solving

Matrix environment

AI automation usage

Multitasking

Education

Bachelor’s degree in life sciences

MSc/PhD (desirable)

Job description

ICON is seeking a Global Study Manager to be fully integrated in the FSP clinical operations team and deliver global clinical studies. This permanent, home-based role requires managing study activities, vendors, budgets, and regulatory compliance across regions.

You will contribute to risk management, quality assurance, and documentation while collaborating with internal teams and external partners. Advanced degree is desirable.