Poland - Clinical FSP Quality Manager

IQVIA Inc; Warszawa; On-site; PLN 151,000 - 374,000; Full time

Job summary

IQVIA Inc in Poland is seeking a seasoned Quality Management professional to join our Delivery Unit and sponsor teams in Warsaw. You will define and adopt the global Quality Plan, ensure GCP compliance and risk management, and guide corrective/preventive actions to improve staff performance and processes.

You will collaborate with global/ regional Quality Management and other stakeholders to monitor KPIs, implement SOPs, and advise on quality control across clinical staff and projects.

Qualifications

• Bachelor's degree or equivalent qualification is required.
• At least 7 years of overall working experience.
• At least 3 years of extensive GCP experience.
• Knowledge of regulatory and drug development processes.
• Experience in CRO or pharmaceutical operations.
• Strong organizational and communication skills.
• Ability to travel within the region/country.
• Ability to lead and motivate a clinical team.
• Strong stakeholder management and interpersonal skills.

Responsibilities

• Adopt and implement the global Quality Management Plan within the assignment scope.
• Identify risks and support corrective/preventive actions.
• Collaborate with stakeholders to maintain quality focus in projects.
• Develop and monitor a Delivery Unit/ Sponsor quality plan and risk program.
• Provide guidance on GCP compliance and quality issues.
• Assist audits and regulatory inspections as agreed.
• Serve as primary Quality Assurance contact for quality matters.
• Prepare periodic quality reports for business lines.

Skills

Fluent in English

Education

Bachelor's Degree or equivalent qualification

Job description

Job Overview

This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s), functional teams, and other stakeholders in a joint effort to clearly define the global Quality Plan, carry out, and adopt the plan according to the specific needs defined by the scope of assignment, assist staff in improving compliance with relevant International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), Key Performance Indicators (KPIs), applicable regulatory requirements, and guidelines. This role provides advice and supports clinical staff and other relevant key stakeholders with regard to quality control, risk management, and corrective/preventive actions.

Essential Functions

• Adopt and implement the global Quality Management Plan within the scope of the assignment, this will include: Planning and executing the Quality Management activities. Risk identification and assessment through data review and quality control processes. Providing support in risk mitigation, in planning corrective/preventive actions, and guidance for improvement. Supporting the assigned business line management and staff to enhance effectiveness.;
• 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, monitor the implementation and delivery.
• 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 in close cooperation with teams to manage non-compliance, quality issues, support in planning corrective/preventive actions, as applicable according to Standard Operating Procedures (SOPs.); Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.; Inform Quality Management, the assigned business line, and Quality Assurance of quality issues according to SOPs.
• Work closely with Quality Assurance and assigned business staff in case of suspected misconduct, as required by the applicable SOPs.
• May provide assistance during audits and regulatory inspections to the teams to the extent agreed with the business lines, as required by the applicable SOPs.
• Act as the primary contact for Quality Assurance on quality matters - on the level of the assignment, attend meetings/teleconferences.
• Prepare periodic reports to business lines on quality related matters, risk assessments and specific quality improvement initiatives.
• Upon agreement with the line manager: Perform any other reasonable tasks as required by the role.;

Qualifications

• Bachelor's Degree Bachelor's Degree or equivalent qualification Req
• At least 7 years of overall working experience is a must.
• At least 3 years of extensive working experience in Good Clinical Practice (GCP) environment is a must.
• Knowledge of National and International Regulations and Drug Development processes.
• Knowledge of Clinical Research Organization (CRO) or Pharmaceutical industry operations is a must.
• Good organizational, interpersonal and communication skills.
• Excellent problem solving skills.
• Ability to travel within the region/country.
• Ability to lead and motivate a clinical team.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers.
• Fluent in English.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is zł 151.200,00 - zł 374.100,00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.