Senior Clinical Operations Manager

PPD (Thermo Fisher)

UK
Not specified; not specified; comprehensive benefi...
Fully remote
3+ years managing cras
Ich/gcp and fda guidelines knowledge
Ctms and clinical data systems proficiency
PPD (Thermo Fisher) is seeking a Senior Clinical Operations Manager to lead a team of Clinical Research Associates (CRAs) in a fully remote role. The position emphasizes performance management, training, and adherence to standard operating procedures while offering an opportunity to contribute to a company recognized for its commitment to scientific excellence

Job Summary

  • This role involves overseeing a team of CRAs to ensure adherence to company SOPs and regulatory standards while driving end results through key performance indicators.
  • The position requires conducting regular performance appraisals, recruiting staff, and facilitating training programs to meet operational needs across multiple countries.
  • Employees benefit from comprehensive health and wellbeing programs, flexible work arrangements, and access to continuous learning opportunities via Thermo Fisher Scientific University Plus.

Matching Summary

Match Score: 85

PPD (Thermo Fisher) is seeking a Senior Clinical Operations Manager to lead a team of Clinical Research Associates (CRAs) in a fully remote role. The position emphasizes performance management, training, and adherence to standard operating procedures while offering an opportunity to contribute to a company recognized for its commitment to scientific excellence.

Salary

Not specified; Not specified; Comprehensive benefits including wellness programs and paid volunteer time

Skills & Requirements

Must-have

  • 3+ years managing CRAs
  • ICH/GCP and FDA guidelines knowledge
  • CTMS and clinical data systems proficiency
  • Remote and on-site monitoring skills
  • Performance management and coaching

Nice-to-have

  • Process improvement initiative experience
  • Strong negotiation and conflict resolution
  • Bid support and business development input
  • Risk-based monitoring approach understanding
  • Strategic planning collaboration skills

Key Requirements

  • Minimum 3+ years managing CRAs
  • 5+ years relevant clinical trials experience
  • Knowledge of ICH/GCP and FDA regulations

Work Rights

Not specified

Tailored Resume

Cover Letter