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ACM Global Laboratories

Clinical Trials Scientific Affairs Supervisor

ACM Global Laboratories

. Manage daily departmental performance, resources, task prioritization, and metrics .

Posted 10/5/2026full-timeRemote • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical laboratory operations, including managing departmental performance, overseeing team workload, and ensuring compliance with clinical trial protocols. Proficient in developing training materials and providing mentorship while maintaining strong relationships with internal and external partners.

Highest-signal resume keywords
Clinical Laboratory ExperienceTeam LeadershipProject ManagementMT (ASCP) CertificationInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Laboratory ScienceProtocol Testing RequirementsPricing Document ReviewOperational Problem-SolvingGeneralist Laboratory Experience
Soft Skills
Time ManagementOrganizational SkillsPositive MindsetCoaching and MentorshipTeam Collaboration
Tools & Technologies
Microsoft Office
Certifications & Qualifications
MT (ASCP) Certification
Industry Keywords
Clinical TrialsRegulated EnvironmentSOPsReferral LaboratoriesTalent Management

About the role

Key responsibilities & impact
  • Manage daily departmental performance, resources, task prioritization, and metrics
  • Oversee the team's day-to-day workload
  • Hire, coach, train, develop, and performance-manage direct reports
  • Serve as an escalation and strategic contact for the department
  • Lead or participate in cross-functional process improvement initiatives
  • Develop and deliver onboarding and continuing education plans and materials
  • Provide coaching, mentorship, performance feedback, and career development plans
  • Partner with HR on talent management, performance, employee relations, and development activities
  • Investigate clinical trial protocol testing requirements and determine appropriate testing facilities
  • Review and prepare pricing documents and correct discrepancies
  • Maintain relationships with ACM and referral laboratories
  • Provide scientific and technical information for client RFPs and RFIs
  • Coordinate testing methods with referral laboratories
  • Obtain and document referred testing information and support referral-laboratory contracting throughout active trials
  • Channel information between Laboratory Operations and Sales
  • Escalate study, testing, and referral-laboratory issues; assist with root cause analysis
  • Improve work methods, efficiency, cost reduction, and operational problem-solving
  • Liaise with internal and external partners and participate in client teleconferences
  • Provide consultation and subject-matter expertise to clinical-trials operations and external clients
  • Update global SOPs and maintain templates and tools
  • Triage upcoming work and determine staffing capabilities and workloads
  • Perform other assigned duties

Requirements

What you’ll need
  • Bachelor's degree in a relevant scientific discipline or a minimum of 3 years of experience as a Clinical Laboratory Scientist
  • Minimum of 5 years of laboratory experience in a clinical setting, or a relevant regulated environment
  • Strong interpersonal and communication skills
  • Strong time management and organizational skills
  • Ability to manage multiple projects with tight deadlines
  • Ability to work independently and in a team setting
  • Proficient in Microsoft Office
  • Generalist laboratory experience
  • Ability to lead and positively motivate others
  • Models a positive and solutions-oriented mindset
  • MT (ASCP) Certification – Preferred
  • Schedule availability: Days, Monday–Friday
  • Ability to respect patient confidentiality and follow company policies and procedures