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ACM Global Laboratories

Associate 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
Quality assurance and regulatory professionals
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£48,200 (£24.72 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: Associate Scientific Affairs Analyst

Department: Scientific Affairs

Location: Remote, United Kingdom

Hours Per Week: 37.5

Schedule: Days, Monday – Friday


SUMMARY

The Clinical Trials PreAward Scientific Affairs Associate Analyst is responsible for the review of study protocols and investigating testing requirements to assist in facilitating the timely response for proposals. Coordinates the testing methods as needed with ACM Research and Development, ACM Laboratory, and referral laboratory partners for study support and set up. Obtains and document testing information throughout the course of the active trial.


RESPONSIBILITIES

  • Investigate testing requirements within a clinical trial protocol and help determine appropriate approach to required testing and associated nuances for the timely and accurate response for proposals.
  • Review pricing documents as needed for any discrepancies
  • Maintain relationship between ACM departments and referral laboratories.
  • Provide scientific/technical information to compile client RFPs and RFIs.
  • Provide feedback to Manager to address analytical trends in support of business needs
  • Assist in coordinating the testing methods as needed with referral labs.
  • Obtain and document referred testing information throughout the course of the active trial, including contracting with referral labs.
  • Assumes responsibility for channeling information to and from Laboratory Operations and Sales.
  • Alert management to issues during the life cycle of studies related to testing needs.
  • Report issues with referral laboratories.
  • Makes suggestions to manager for improved work methods and ways to increase efficiency, reduce costs, and solve operational problems.
  • Understands and follows company policies and procedures and respecting patient confidentiality.
  • Other duties as defined and requested by Operational Management

  • REQUIRED QUALIFICATIONS

    • BS required, laboratory science emphasis preferred, or minimum 2 years of experience as a biomedical scientist


    PREFFERED QUALIFICATIONS

    • 2 yrs clinical trials experience preferred
    • Excellent interpersonal and communication skills
    • Excellent time management and organizational skills
    • Ability to manage multiple projects with tight deadlines