Clinical Trials Scientific Affairs Analyst

Job Title: Clinical Trials Scientific Affairs Analyst

Department: Study Set Up

Location: Remote | United Kingdom

Hours Per Week: 37.5 hours

Schedule: Days;
Monday – Friday

The Clinical Trial Scientific Affairs (CTSA) Post-Award Analyst is responsible for investigating testing requirements and testing facilities to assist in facilitating the timely response for internal study operations team. The CTSM Post Award Analyst has proficient knowledge in laboratory science and assists with process improvement initiatives within Scientific Affairs

• Ensures complete study scoping, including testing requirements, facilities and other nuances
• Provides technical details to ACM study team for study designs and updates
• Provides data support to address analytical trends or issues
• Provides consultation to clinical trials operations and external clients, as needed
• Responsible for channeling information to and from Laboratory Operations and Study Management
• Conducts investigations and assists with implementation of corrective actions, as needed
• Investigates issues during the life cycle of the studies
• Manages low to medium complex assignments
• Assists with special projects, as needed
• Participates in cross functional process improvement initiatives to optimize operational capabilities
• Serves as a laboratory science expert for study optimization
• Participates in quality issue investigations, documentation and resolutions
• Understands and follows company policies and procedures, respecting patient confidentiality
• Performs other duties as assigned

• Bachelor’s Degree
• Minimum 5 year Biomedical Science experience

• Clinical Trials experience
• Strong communication and interpersonal skills
• Ability to multitask, working on multiple projects with tight deadlines