Clinical Trials Scientific Affairs Analyst

ACM Global Laboratories; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical laboratory is seeking a Clinical Trials Scientific Affairs Analyst. This remote position requires a Bachelor's degree and a minimum of 5 years of Biomedical Science experience. The role involves ensuring complete study scoping, providing technical details for study design, and supporting data analysis to address trends. Strong communication and multitasking abilities are essential as you will collaborate with internal teams and external clients on operational optimization. Join us to help improve clinical trial processes and outcomes.

Qualifications

• 5+ years of Biomedical Science experience required.
• Clinical Trials experience preferred.

Responsibilities

• Ensure complete study scoping, including testing requirements and facilities.
• Provide technical details to the study team for study designs and updates.
• Support data addressing analytical trends or issues.

Skills

Strong communication skills

Interpersonal skills

Ability to multitask

Education

Bachelor's Degree

Job description

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

SUMMARY

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

RESPONSIBILITIES

• 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

REQUIRED QUALIFICATIONS

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

PREFERRED QUALIFICATIONS

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