Clinical FSP – Quality Manager

IQVIA

Quality Manager at IQVIA ensuring compliance with GCP and risk management in clinical research projects. Collaborating with global teams to enhance quality control and project delivery.

Posted 5/19/2026full-timeDurham • North Carolina • 🇺🇸 United StatesMid-LevelSenior💰 $86,500 - $216,000 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality Management PlanRisk Management ProgramGood Clinical Practice (GCP)Standard Operating Procedures (SOPs)International Conference on Harmonization (ICH)quality management processesmedical terminologyrisk assessmentsquality improvement initiatives

Soft Skills

cooperationadvice and supportcommunicationfocus on quality

Tools & Technologies

IQVIA corporate standards

Certifications & Qualifications

Bachelor's Degree

Industry Keywords

pharmaceuticalbio-pharmaceuticalClinical Research Organization (CRO)National and International RegulationsDrug Development processes

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Adopt and implement the global Quality Management Plan within the scope of the assignment
Identify and assess risks through data review and quality control processes
Cooperate closely with the relevant business and other stakeholders, support maintaining focus on quality in project delivery
Contribute to the development and implementation of a Delivery Unit/Sponsor specific Quality Management plan and Risk Management Program
Provide advice and support to teams within the assigned business line and other key stakeholders on all aspects of Good Clinical Practice (GCP) compliance
Work closely with Quality Assurance and assigned business staff in case of suspected misconduct
Prepare periodic reports to business lines on quality related matters, risk assessments and specific quality improvement initiatives

Requirements

What you’ll need

Bachelor's Degree
Minimum of 5 years' experience in a pharmaceutical, bio-pharmaceutical, or CRO, or equivalent
Minimum of 3 years' experience in Quality Role
Sound working knowledge of medical terminology, Standard Operating Procedures (SOPs), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), applicable regulatory requirements, quality management processes
Knowledge of National and International Regulations and Drug Development processes
Knowledge of Clinical Research Organization (CRO) or Pharmaceutical industry operations
Knowledge of IQVIA corporate standards and SOPs
Fluent in English

Benefits

Comp & perks

Health insurance
Retirement plans
Flexible work arrangements
Professional development opportunities
Bonuses