Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe. Won’t you join us today as a Principal Quality Assurance Auditor?  

Position Summary: 

The Principal Quality Auditor is responsible for providing senior oversight and subject matter expertise to quality and compliance activities, supporting the Q&C Management team, Q&C team members, and the project teams during all stages of a clinical study.  

Essential functions of the job include but are not limited to:  

Serve as a subject matter expert for clinical project teams  Uses ability and specialized skill to complete difficult tasks. Develops and implements concepts and/or techniques to achieve objectives  Understands Precision processes and functional SME organization to work through complex tasks independently to resolution  Support the Quality Management System including SOPs, training and CAPA   Attends project meetings, representing Quality. Reviews project plans and provides compliance guidance on complex issues independently.   Process and maintain documentation for controlled documents, as required   Develop and administer training for employees and/or consultants   Host client/sponsor audits and support regulatory inspections   Coordinate and conduct assessments of potential and contracted vendors, including vendor audits as warranted   Coordinate and conduct internal audits of quality systems   Coordinate and conduct investigator site audits   Coordinate and conduct trial master file audits   Participate on computer systems validation projects and systems change control process   Monitor quality systems to provide feedback on compliance risks to QA management and identify opportunities for improvement   Maintains Q&C trackers, databases, metrics, and files   Follow applicable regulations and standards, including but not limited to local regulations (US FDA and EU), ICH and company policies and procedures   Support Proposals and Bid Defense meetings as needed  Additional tasks as required  

Qualifications: 

Minimum Required: 

5 years of experience  Working knowledge of GCP/ICH guidelines and FDA regulations and standards   Audit experience conducting a variety of audit types, including internal systems, vendors, TMF and investigator site audits. 

Other Required: 

Bachelor’s degree in a science, healthcare, or related field of study; combination of qualifications and equivalent relevant experience may be accepted as an alternative  Availability to travel up to 25% domestically and/or internationally  

Preferred: 

CRO, Pharmaceutical and/or Medical device experience   QA certification preferred (e.g., CQA, SQA, etc.)   Experience with electronic clinical trial systems (e.g., EDC, CTMS, IxRS, ePRO, etc.)  

Skills: 

Excellent interpersonal and problem-solving skills, effective verbal and written communication, computer skills 

Competencies  

Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient.   Demonstrates mastery knowledge of ICH-GCP, relevant Precision SOPs, and compliance guidance, as well as the ability to implement   Proficient in Microsoft Word, Excel, and PowerPoint   Ability to support senior leadership in Q&C Management tasks and projects, offering solutions and processes for increased efficiencies within the department.   Ability to develop, coach and mentor Q&C staff.   Demonstrates a solid working knowledge of e-Clinical systems/platforms.   Demonstrates strong interpersonal skills.   Ability to lead and inspire excellence within a team   Results oriented, accountable, motivated and flexible   Exhibits strong self-motivation, is detail-oriented and able to work and plan independently as well as in a team environment.   Demonstrates professionalism, as evidenced by punctuality, ability to deliver on commitments, possess good. interpersonal skills and maintain positive interactions with internal and external stakeholders.   Demonstrates values and a work ethic consistent with Precision Values and Company Principles.   Excellent verbal and written communications skills 

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