Clinical Quality Operations Manager

We are currently seeking a Clinical Quality Operations Manager!

This is a full-time hybrid role based within Canada. This individual will need to be located in Canada Fluent in French and English and willing to go into the Montreal/Kirkland office twice a week.

If you join us you will work with some of the worlds leading pharmaceutical biotechnology and medical device companies in a vital stage of clinical development: establishing the safety tolerability and pharmacokinetics of a new drug.

WHAT YOU WILL DO

You will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Key responsibilities:

• It is critical that for all sponsor-sponsored clinical trials patient safety high quality data and compliance with company requirements and regulations are delivered and sustained. The CCQM position has a significant impact in achieving those objectives.
• Under the guidance of the Regional Director Clinical Quality Management (RCQM) the CCQM oversees all CQM activities in the respective country/cluster.
• The role requires the ability to properly implement local/global processes/procedures to identify opportunities for process improvement and to support continuous improvement addition the CCQMs support audits inspections as well as Quality Control and local training activities.

YOU NEED TO BRING

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

Experience:

• A minimum of 6-8 years of relevant experience in clinical research including direct field monitoring experience or management/oversight of such individuals with a demonstrated record of accomplishments. Experience in Country Operations preferred.
• Deep knowledge and understanding of Clinical Trial processes GCP and other clinical research related regulations.
• Solid track record of initiating planning and delivery of projects and knowledge of project management practices.
• Demonstrated experience in leading cross-functional teams.
• Experience in Clinical Quality Management including Quality Control Activities Process Management & Improvement.
• Experience in managing audits and inspections.
• Experience in coordinating and delivering training sessions.

Skills:

• Superior oral and written communication and leadership skills in an international environment.
• Excellent project management organizational and prioritization skills.
• Excellent teamwork skills including conflict resolution expertise and discretion.
• Ability to analyze interpret and solve complex problems.
• Ability to think strategically objectively and with creativity and innovation.
• Ability to proficiently interact with all levels of clinical research management and exert influence to achieve results.

Regulations & Processes:

• Local expert for ICH-GCP and local regulations (incl. impact assessment of new/updated local regulations on local processes).
• In close collaboration with local country operations management manages the local network of owners / Subject Matter Experts (SMEs) for global/local processes to ensure a proper implementation of global/local processes and the regular update of local Standard Operating Procedures (SOPs) / Work Instructions (WIs).
• Local expert for any quality-related local processes.
• Identifies process gaps / opportunities for process improvement and properly escalates to RCQM and/or Global Process Owners (if necessary).
• Leads continuous quality improvements activities at the country level as agreed with Country/Cluster CRD and RCQM and supports or co-leads continuous improvements activities at the global/regional level.

Training:

• Local training point of contact and the liaison between local country operations and client Learning & Development (L&D).
• In close cooperation with local country operations management identifies / coordinates local training needs.
• Supports local trainings (as needed).

Quality Control (QC) Activities:

• In conjunction with the local country operations management coordinates and oversees all QC activities. This includes to ensure a proper execution of the In-house Quality Control Plan (IHQCP) the Quality Control Visits (QCVs) as well as any other QC Checks.
• In mutual agreement with local country operations management and the RCQM performs QC activities (incl. QCVs) and conducts ad hoc site visits upon request.
• On a regular basis and in collaboration with local country operations identifies local trends performs root-cause-analysis (if necessary) develops local action plan (incl. sharing of results and training of local country operations if required).

Audits & Inspections:

• Primary local point of contact for sponsor Quality Assurance and Regulatory Agencies.
• Manages and supports activities during the preparation / ongoing / follow-up phase of an audit or inspection.
• In cooperation with local country operations and/or headquarters performs root-cause-analysis for audit observations/inspection findings manages and tracks the Corrective and Preventive Actions (CAPAs) and coordinates/facilitates the responses to audit/inspection reports.
• On a regular basis and in collaboration with local country operations identifies local trends performs root-cause-analysis (if necessary) and develops local action plan (incl. sharing of results and training of local country operations if required).

Quality / Compliance / Privacy Issue Escalation:

• Communicates/escalates quality/compliance issues (incl. any potential trends) to local country operations management and RCQM.
• Escalates significant quality/compliance issues and supports investigations (fact finding root-cause-analysis) as well as the reporting of Serious Breaches if applicable.
• Serves as local POC or supports local POC in case of escalations/reporting of Privacy Incidents if applicable.

Clinical Supplies GCP Investigations

• Evaluates trends on Clinical Supply GCP Inquiries and incorrect management of clinical supplies.
• Coordinates GCP Investigations of trends related to Clinical Supply GCP Inquiries and incorrect management of clinical supplies (if necessary).

Supplier Qualification:

• Leads local supplier qualifications and re-qualifications of locally selected suppliers and supports solving of quality issues with locally selected suppliers.
• Supports the Quality Management System (QMS) assessment for local supplier qualifications and re-qualifications.

Sponsor Compliance & Privacy Steward:

• Supports implementation of divisional compliance/privacy initiatives and reporting at the local level.
• Communicates compliance/privacy concerns to local legal/compliance/privacy department and/or sponsor Compliance/Global Privacy Office.

Global / Regional Key Initiatives / Projects

• Supports global/regional key initiatives/projects upon request of the RCQM.

What do you get

Regular full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

• Medical Dental Vision Life STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERGs (employee resource groups)

Physical Demands/Work Environment:

• Work Environment:

• Work is performed in an office environment with exposure to electrical office equipment.
• Frequent travel to clients/ site locations with occasional travel both domestic and international.

• Travel requirements: 15%

  Physical Requirements:

• Ability to sit for extended periods and operate a vehicle safely.
• Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists.
• Occasional crouching stooping with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Learn more about our EEO & Accommodations request here.