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Thermo Fisher Scientific

Manager, Clinical Operations

Thermo Fisher Scientific

. Lead the clinic operations team .

Posted 10/13/2026full-timeBrussels • BelgiumMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical operations management, ensuring compliance with ICH/GCP and FDA regulations while optimizing patient care processes. Proven ability to lead teams, manage performance, and facilitate training and development in a clinical research environment.

Highest-signal resume keywords
Clinical Research Associate ExperienceLeadership ResponsibilityExpert Knowledge of ICH/GCP and FDA GuidelinesPerformance Management AbilitiesEffective Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Operations ManagementProcess OptimizationRegulatory ComplianceStaff Training and DevelopmentPerformance ManagementTime ManagementAttention to DetailMicrosoft Office Proficiency
Soft Skills
Strong Organizational SkillsExcellent Judgment and Decision-MakingInterpersonal SkillsProblem-Solving AbilityMotivational Skills
Certifications & Qualifications
Bachelor's Degree or Equivalent
Industry Keywords
Healthcare RegulationsPatient Care StandardsVolunteer Safety RequirementsStudy-Award ProbabilityDepartmental Activities

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Lead the clinic operations team
  • Oversee day-to-day clinic activities and ensure high standards of patient care
  • Optimize processes and ensure compliance with healthcare regulations
  • Plan and coordinate general departmental activities
  • Work with Team Leaders on clinical team activities
  • Analyze and evaluate departmental efforts, including clinic adequacy and quality
  • Liaise with the medical director during feasibility processes to ensure volunteer safety requirements are addressed in scheduling
  • Manage internal and external communication and evaluate bed-space information to increase study-award probability and meet client deliverables
  • Oversee staff training and development and direct workflow for complex processes
  • Work with management to provide clinical team training and study-placement awareness
  • Manage staff, including interviewing, selection, job description preparation, professional development, goal setting, performance management, coaching, mentoring, counseling, and separations
  • Approve salary administration, hiring, corrective action, and termination decisions
  • Review and approve time records, expense reports, leave requests, and overtime

Requirements

What you’ll need
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • 5+ years of previous experience providing relevant knowledge, skills, and abilities
  • Ideally 1+ year of leadership responsibility
  • Experience working as a Clinical Research Associate required
  • Expert knowledge of relevant regulations, including ICH/GCP and FDA guidelines
  • Strong organizational skills
  • Performance management abilities
  • Excellent judgment and decision-making skills
  • Effective oral and written communication skills
  • Strong interpersonal skills and problem-solving ability
  • Time management skills
  • Attention to detail
  • Good computer skills, including Microsoft Office
  • Ability to motivate and integrate teams and teach/mentor team members
  • Ability to work remotely anywhere in Belgium and attend one office day on Tuesday
  • Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered

Benefits

Comp & perks
  • Global team environment
  • Career development opportunities
  • Resources to achieve individual career goals
  • Collaboration and development opportunities
  • Scientific excellence-focused work environment