Clinical Quality Assurance Specialist Ii

Detalles de la oferta

**Work Schedule**Standard (Mon-Fri)**Environmental Conditions**OfficeWhen you are part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals.**Summarized Purpose**:Conducts internal computer system validation deliverable reviews to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identifies issues impacting quality and/or regulatory compliance, determines root cause of non-conformance and develops strategies to address issues. May perform technical document review and other GxP activities in support of ISQA project work or company process.**Essential Functions and Other Job Information:**Job Description**:Responsibilities will include the reviewing and approving of Computer System Validation documentation to succeed in the:- Facilitation of closure of the more than 500 gaps identified due to the EMA Guideline on computerized systems and electronic data in clinical trials- Reviewing and approving End User Tool documentation (Power BI dashboards, spreadsheets, reports, etc.)- Reviewing and approving Audit Trail Review Plans and supporting documentation- Supporting additional computer system validation initiatives within the ISQA Computer Validation Compliance team, as required**Knowledge, Skills and Abilities**:Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.- Thorough knowledge of applicable GxP regulations, including 21 CFR Part 11, EMA, ICH and appropriate regional regulations- Strong computer skills; ability to learn and become proficient with appropriate software- Firm knowledge of Power BI/apps experience- Good knowledge of SOPs and WPDs- Excellent oral and written communication skills (including appropriate use of medical and scientific terminology)- Strong attention to detail- Effectively works independently or in a team environment- Effective problem solving skills- Solid organizational and time management skills including ability to multitask and prioritize competing demands/work load- Proven flexibility and adaptability**Our 4i Values**:Integrity - Innovation - Intensity - Involvement


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

Requisitos

Clinical Research Associate Ii

**More about you**On your first day we'll expect you to have:- Site Management or equivalent experience in clinical research, with understanding of clinical ...


Parexel - Tamaulipas

Publicado 11 days ago

Research Consultant

.**Fòs Feminista**Fòs Feminista is an intersectional feminist organization centered around the sexual and reproductive health and rights of women, girls, and...


Fos Feminista - Tamaulipas

Publicado 11 days ago

Study Start Up Associate I

.At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to adv...


Icon - Tamaulipas

Publicado 11 days ago

Desarrollador De Negocios

**Cápita Works** was founded in 2020, amid a global pandemic, to provide people with remote jobs to work from home and offer small and medium-sized companies...


Cápita Works - Virtual Assistants In Mexico - Tamaulipas

Publicado 11 days ago

Built at: 2024-12-12T08:27:39.323Z