Quality Assurance Manager

TOTAL TRIALS INC • US,

1d • $70,000 - $108,000 • Onsite

About The Position

The Quality Assurance Manager assists the Global Head Quality and Compliance with the development and implementation of a broad spectrum of quality activities to demonstrate, document, and report compliance with client expectations in accordance with relevant guidelines and regulations. The Quality Assurance Manager may also assist with training compliance and document administration by helping to coordinate the flow of documents through ZenQMS, ensuring compliance with training curricula, and tracking and trending associated metrics.

Requirements

• Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint
• Knowledgeable in the content and application of clinical research processes, GxP, and other relevant requirements of major regulatory agencies (e.g., FDA, EMA, PMDA, SAHPRA).
• Highly effective oral and written English communication skills.
• Strong time management, follow-up, and organizational skills, with specific emphasis on attention to detail
• Problem solving/process improvement skills with the ability to be part of and own solutions
• Ability to work well independently, as part of a team, and in a coaching role.
• Bachelor’s Degree or the equivalent
• At least 6 years in a clinical research setting with increasing Quality Assurance responsibility is required.
• Proficiency with Microsoft Office applications (e.g., MS Word, MS Excel, MS PowerPoint, MS Teams, MS Power BI, as applicable)
• Experience with ZenQMS or similar document repository system
• valid driver’s license and passport
• ability to travel

Nice To Haves

• Experience in a dedicated auditing role.

Responsibilities

• Maintain knowledge of current and new regulations and guidelines and assist with their integration into the Total Trials Global Quality Management System.
• In coordination with functional leadership, develop and maintain policies and procedures that align with Total Trials mission and values, ICH GCP guidelines, and relevant regulations.
• Develop and implement internal audit plans according to the QMSS Annual Work Plan, performing internal audits as assigned to assess and monitor compliance with Total Trials Standard Operating Procedures, Policies, and study-specific plans.
• Develop and implement audit plans as assigned for fulfillment of contractual obligations and vendor qualification requirements.
• Serve as co-host of audits of FHI Clinical, assisting with coordination of documents and presentations before, during, and after audits. Assist with the coordination and review of audit responses from various functional areas.
• Serve as a GCP and regulatory resource to the project teams, assisting with quality oversight of projects, including tracking and trending of quality and risk metrics, as assigned.
• Other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior