Global Study Manager - Cardiovascular Trials Lead

Remote Worker LTD.; United States; À distance; USD 93 000 - 146 000; Plein temps

Avantages offerts par ce poste

Competitive base salary

Wellbeing programmes

Retirement and pension plans

Life assurance and disability

Training and career development

Résumé du poste

ICON Strategic Solutions is seeking a Global Study Manager to lead and deliver global clinical studies from protocol to close-out, coordinating with cross-functional teams, CROs, and vendors to ensure high quality, on-time results and regulatory compliance. The role focuses on cardiovascular programmes and global trial execution across geographies.

The successful candidate will bring life sciences expertise, 3+ years in global trial management, and strong stakeholder communication, working in a

Qualifications

• Degree in Life Sciences, Medical Sciences, Biological Sciences or related field.
• 3+ years global trial management experience in clinical research, pharma or CRO.
• Strong understanding of clinical development and drug development process.
• Excellent knowledge of ICH-GCP and global trial regulations.
• Proven project management and organisational skills.
• Strong stakeholder management and communication skills.
• Experience in global cross-functional teams.
• Cardiovascular trials experience desirable.

Responsabilités

• Support delivery of global clinical studies from protocol development to close-out and archiving.
• Collaborate with internal stakeholders, CROs and external vendors globally.
• Ensure studies are delivered on time, within budget, and with high quality and compliance.
• Contribute to innovative programmes, including cardiovascular trials.

Connaissances

Global trial management

Stakeholder management

Cross-functional teamwork

Communication skills

Independent working

Formation

Life sciences degree

Description du poste

ICON Strategic Solutions is seeking a Global Study Manager to lead and deliver global clinical studies from protocol to close-out, coordinating with cross-functional teams, CROs, and vendors to ensure high quality, on-time results and regulatory compliance. The role focuses on cardiovascular programmes and global trial execution across geographies.

The successful candidate will bring life sciences expertise, 3+ years in global trial management, and strong stakeholder communication, working in a