SR Project Coordinator

Thermo Fisher Scientific; São Paulo; Teletrabalho; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A Thermo Fisher Scientific está em busca de um Coordenador de Projetos Sênior para se juntar à equipe de Suprimentos Clínicos. O profissional apoiará as operações administrativas, garantindo que a documentação regulatória esteja correta e organizada, além de colaborar na manutenção de repositórios de dados. Uma ótima oportunidade de crescimento em um ambiente inovador e colaborativo.

Serviços

Remuneração competitiva

Bonus anual

Assistência médica

Várias vantagens para empregados

Qualificações

• Experiência anterior que forneça os conhecimentos e habilidades necessárias para desempenhar a função.
• Idealmente experiência em ensaios clínicos e cadeia de suprimentos clínica.

Responsabilidades

• Fornecer apoio administrativo e técnico à equipe de Projetos de Suprimentos Clínicos.
• Manter documentação, procedimentos e registros de projetos.

Conhecimentos

Interpersonal Skills

Organizational Skills

Problem Solving

Attention to Detail

Leadership Skills

Customer Service

Formação académica

High / Secondary school diploma or equivalent

Relevant formal academic / vocational qualification

Ferramentas

Microsoft Office Suite

Descrição da oferta de emprego

Join to apply for the SR Project Coordinator role at Thermo Fisher Scientific

Join to apply for the SR Project Coordinator role at Thermo Fisher Scientific

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

The role

We are seeking a Senior Project Coordinator to join our Global Clinical Supplies Team. This role can be fully homebased.

A day in the life

Provides administrative and technical support to our Global Clinical Supplies Project Team including planning, organizing and coordinating responsibilities of project administration. Maintains procedures, guidelines and documentation. Assists with maintaining project records and ensuring that all regulatory documents are correct, processed and approved. Completes data entry and supports maintenance of data base repositories. Assists in preparing reports and data collection for analysis. Supports quality review.

Key responsibilities:

• Assists with review, coordination and compilation of files and other materials.
• Distributes project documents and supplies.
• Processes and tracks local regulatory, study specific or department documents. Maintains trackers.
• Performs file reviews. Organizes and maintains correspondence files and other departmental records.
• Analyzes and reconciles project documents, metrics and findings reports within specified timelines.
• Assists with clarification and resolution of findings related to documentation.
• Composes, uploads, and distributes communications, reports, documents and forms.
• Provides accesses to company, client and vendor systems.
• Assists on project management ad-hoc activities, producing reports or on study
• plan edition.
• Coordinates and schedules team calls
  
  

Keys to success:

Education and experience:

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
• Technical positions may require a certificate
• Previous experience that provides the knowledge, skills, and abilities to perform the job
  
  

Knowledge, Skills and Abilities:

• Ideally experience in Clinical trials
• Ideally experience with Clinical Supply chain
• Strong English and interpersonal skills both written and verbal
• Strong interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills
• Effective leadership and team building skills
• Strong solid understanding of Microsoft Office suite
• Strong attention to detail
• Ability to work in team environment, as well as work independently with guidance
• Ability to provide customer service with the highest standards of quality and excellence
  
  

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Production, Supply Chain, and Manufacturing

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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