Senior Study Specialist - Global Clinical Operations

BioMarin Pharmaceutical Inc.; United Kingdom; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology company based in the United Kingdom is seeking a Sr. Study Specialist to lead oversight tasks related to site monitoring and vendor management. The ideal candidate should have a BA/BS or higher in nursing, life or health sciences and experience in a biotech or pharmaceutical environment. This role includes responsibilities such as developing study documentation and managing external vendor relationships, with a focus on ensuring data integrity and quality throughout the study lifecycle.

Qualifications

• Experience in a biotechnology or pharmaceutical company.
• Oversight of external vendors including SOW, budgets, POs, and invoice management.

Responsibilities

• Develop study specific documentation.
• Contribute to the oversight of country and site feasibility assessment.
• Oversight of CRO for IRB/EC related submission/approval activities.
• Develop/Oversee site and investigator training materials.
• Attend Global Study Operations team meetings as GSO representative.

Skills

Agility and Proactivity

Leadership

Communication and Collaboration

Education

BA/BS or higher in nursing, life or health sciences

Tools

DocuSign

Job description

A leading biotechnology company based in the United Kingdom is seeking a Sr. Study Specialist to lead oversight tasks related to site monitoring and vendor management. The ideal candidate should have a BA/BS or higher in nursing, life or health sciences and experience in a biotech or pharmaceutical environment. This role includes responsibilities such as developing study documentation and managing external vendor relationships, with a focus on ensuring data integrity and quality throughout the study lifecycle.