Clinical Quality Manager. Madrid. Sponsor dedicated

hace 2 semanas

Madrid, Madrid, España Syneos Health A tiempo completo

Manager, Quality Assurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we're able to create a place where everyone feels like they belong.

Job Responsibilities

General Profile

Conducts audits in accordance with QA SOPs and WIs and oversees the conduct of audits. Responsible for generating own and reviewing others' audit reports. Prepares for and hosts or supports customer audits in accordance with QA SOPs and WIs. Coordinates responses to customer audits of investigator sites, and resolves issues with customers, where applicable. Plans and provides strategies for assessing readiness of Syneos Health offices for potential Regulatory Inspections and conducts such assessments (e.g. develops a program for and conducts 'mock inspections'). Develops and delivers inspection readiness training to staff. Prepares for and hosts or supports Regulatory Authority Inspections in accordance with QA SOPs and WIs. Coordinates the preparations and activities for inspections by Regulatory Authorities, including compilation of any pre-inspection required information. Communicates findings from customer audits and Regulatory Authority Inspections of Syneos Health promptly to appropriate Syneos Health personnel and provides support on root cause analysis, corrective and preventive actions. Provides consultancy on quality related matters as needed. Builds and maintains an organization that meets the needs of Syneos Health and its customers and ensures that his / her direct reports deliver against the budget, timeline, and quality requirements. Assigns local staff to Corporate Quality projects and supports the staff in project execution. Line management responsibilities for staff members. For direct and indirect reports, may participate and direct activities related to department staff operations such as interviewing and selection, professional development, performance management, employee counseling and separations. Works with and advises staff on administrative policies and procedures, technical problems, priorities and methods.

Functional and Technical Expertise

Knowledge of Medical and technical terminology related to the audit types to be conducted.

Complexity

Anticipates and resolves key technical, operational, or business problems related to non-compliance with GxP. Applies critical thinking to identify solutions to non-standard requests and complex problems. Well versed in personnel management, customer management and project management.

Supervision

Supervises a team of auditors.

Qualifications

What we're looking for

Requires a Bachelor's degree in a science/health care field or equivalent with significant experience and expertise in all aspects of GxP quality assurance auditing. Previous experience in the conduct of multiple audit types (e.g. vendors, investigator sites, trial master files, data management, safety reporting, and laboratories) is essential. Excellent knowledge of GxP regulatory requirements. Computer literacy commensurate with job requirements (Microsoft Office suite; basic Sharepoint proficiency). Able to act independently and proactively. Above average attention to detail. Able to handle multiple tasks to meet timelines in a dynamic environment. Strong organizational, presentation and interpersonal skills. Excellent team building skills. Cultural sensitivity to allow effective communication with stakeholders from diverse cultural backgrounds. Ability to negotiate and provide constructive feedback. Well-developed communication skills and the ability to write concise, accurate reports and other necessary documentation.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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