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Fortrea · 1 day ago

FSP - Assistant Clinical Quality Control Manager

United States

Full-time

Remote

Mid Level

$135K/yr - $148K/yr

3+ years exp

Fortrea is seeking an Assistant Clinical Quality Control Manager for their FSP team, which is home based in the US. The role is responsible for tracking, processing, and reporting Quality Control data, collaborating with various stakeholders to enhance quality management processes.

Clinical TrialsHealth Care

H1B Sponsor Likely

Responsibilities

As assigned, support the development of the functional/regional quality plan outlining processes, metrics, roles, and responsibilities

Support the development of functional processes that will be used to evaluate and identify performance trends that indicate the need for process improvement. This will include maintenance of a Quality Dashboard for reporting purposes to functional managers and leadership

Under guidance by the LM, identify important trends and best practices in quality management in the organization that need to be implemented globally. Develop effective ways to communicate these trends and practices throughout the organization to ensure maximum benefit is realized

As assigned, deliver training to functional stakeholders on quality control processes

As assigned, monitor compliance with quality control processes and develop plans to close compliance gaps

As assigned, monitor quality results against our KQI targets to ensure performance is acceptable. If performance is unacceptable or when significant unresolved quality concerns exist, support communication to senior management. As assigned, support the implementation of corrective action plans when performance gaps exist for KQIs

As assigned, deliver training related to quality control tools as required

All other duties as needed or assigned

Qualification

Quality ControlClinical ResearchData AnalysisProject ManagementComputer LiteracyFluent in JapaneseCommunication SkillsOrganizational SkillsTime Management

Required

University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)

In lieu of the above requirement, candidates with one (3-5) or more years of relevant experience in pharmaceutical or CRO industries will be considered

Fortrea may consider relevant and equivalent experience in lieu of educational requirements

Basic understanding of clinical research terminology and ICH-GCP

Ability to interact and engage employees across the globe

Excellent organizational and time management skills

Good communication skills, oral, and written

Good computer literacy. Knowledge of Excel and the ability to generate presentation slides is essential

Preferred

In lieu of the above requirement, candidates with one (3-5) or more years of relevant experience in pharmaceutical or CRO industries will be considered

One (1) or more years of experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management, technical writing, or business development)

Benefits

Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

401(K)

Paid time off (PTO)

Employee recognition awards

Multiple ERG’s (employee resource groups)

Company

Fortrea

Fortrea is a provider of comprehensive Phase I through IV clinical trial management, clinical pharmacology, patient access solutions.

Founded in 2023

Durham, North Carolina, USA

10001+ employees

https://www.fortrea.com

H1B Sponsorship

Fortrea has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2025 (14)

2024 (25)

2023 (6)