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ACM Global Laboratories

Clinical Trials Scientific Affairs Analyst

CompanyACM Global Laboratories
LocationUnited Kingdom
Posted At2/26/2026

UK Visa Sponsorship Analytics

Analytics are greyed out due to low classification confidence (42.0%).
Occupation Type
Biochemists and biomedical scientists
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£45,900 (£23.54 per hour)
Occupation rate applies

Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.

Disclaimer: Hunt UK Visa Sponsors aggregates job listings from publicly available sources, such as search engines, to assist with your job hunting. We do not claim affiliation with ACM Global Laboratories. For the most up-to-date job details, please visit the official website by clicking "Apply Now."

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 1 year Biomedical Science experience AND clinical trials experience OR 2 years Biomedical Science experience


    PREFERRED QUALIFICATIONS

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