Senior Auditor, Clinical Quality and Compliance


The role of the Sr. Auditor, Clinical Quality and Compliance is to act as lead person in the establishing audit plans, assessing/securing compliance in study conduct and to provide strong support to operations via GxP consultation.

 

This role will be perfect for you if:

 

  • You approach challenges with an understanding of norms and regulations, combined with a creative and inquisitive mind
  • You enjoy working with a small team, contributing your experience and expertise to complete a variety of tasks , including special projects
  • You love being a mentor in different types of audits

 

RESPONSABILITIES

 

More specifically, the role of Sr Auditor, Clinical Quality and Compliance includes:

 

  • Implement robust audits plan and execute audits in accordance with the established audit program.
  • Act as a lead/mentor for the conduct of audit activities (site, studies, internal and vendors). Performs review of audit of reports issued by the auditors.
  • Coordinate and conduct clinical sites audit with the project management team. Where applicable, facilitate the audit with the external auditors.
  • Participate in the auditor’s training in providing guidance on audit techniques, risk assessment and system approach.
  • Formulate observation/recommendations and review appropriateness of audit responses/CAPA plan and track progress.
  • Review and assess non-compliances, adequacy of CAPA plan and track the progress of action items. Lead thorough and complete investigations where needed.
  • Provide solid recommendation/guidance via GxP consultation and support auditor in their consultation as needed.
  • Organize and hosts sponsor’s study audits and regulatory inspections including mock inspection activities.
  • Work closely with the Quality Systems group for internal, vendor audits and periodic risk review of vendors. Can also be involved in client’s qualification audits and review of SOPs.
  • Develop training content for topics related to SOP, regulations and GxP. Can provide training to Innovaderm employees.
  • Employee may be assigned to other responsibilities that do not pertain to their former description, if they have the required experience, are qualified and/or have received adequate training.

REQUIREMENTS

 

Education

  • Bachelor degree in a relevant discipline or equivalent experience;

 

Experience

  • 5-10 years’ experience in the pharmaceutical or research industry (more specifically in clinical quality)

 

Knowledge and skills

  • Excellent knowledge of ICH guidelines, FDA and Health Canada regulations and EU standards
  • Master the overall audit process and risk determination
  • Ability to communicate effectively both orally and in writing
  • Good organization skill and ability to adapt to a rapidly growing environment
  • Bilingual: French and English, written and spoken
  • Good knowledge of the Microsoft Office Suite (Word, Excel, PowerPoint)
  • Willing to travel 10-30% of the time

OUR COMPANY

The work environment

At Innovaderm, you will work with brilliant and driven colleagues. Our values are integrity, commitment and teamwork. We offer a stimulating work environment and attractive advancement opportunities. 

 

As a Senior Auditor, Clinical Quality and Compliance, you will be eligible for the following perks: 

  • Flexible work schedule
  • Permanent full-time position
  • Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
  • Offices near public transportation (Sherbrooke metro station or Saint-Laurent metro station)
  • Ongoing learning and development

 

About Innovaderm 

Innovaderm is a contract research organization (CRO) specialized in dermatology with a team of over 350 employees. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America. 

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. 

 

We thank you for your application and please note that only those selected for an interview will be contacted. 

 

Innovaderm only accepts applicants with a work permit for Canada. 

 

 

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