Clin Ops Delivery Specialist I

Thermo Fisher Scientific; São Paulo; Presencial; BRL 40.000 - 80.000; Tempo integral

Resumo da oferta

An established industry player is seeking a Clin Ops Delivery Specialist I to join their dynamic team. This role offers the opportunity to work independently while collaborating with study teams to analyze and optimize clinical trial data. The ideal candidate will possess strong analytical and communication skills, with a background in life sciences or engineering. As part of a supportive environment, you will engage in continuous learning through mentorship and contribute to impactful projects in the pharmaceutical and biotechnology sectors. If you're ready to make a difference in clinical research, this position is for you.

Qualificações

• Bachelor's degree in life sciences or related fields is required.
• Prior clinical research experience is preferred but not required.

Responsabilidades

• Review subject data and identify trends and risks.
• Prepare and analyze clinical trial datasets.
• Lead multidisciplinary discussions and manage escalations.

Conhecimentos

Understanding of database structures

Proficiency in Microsoft Excel

Data review and quality control

Attention to detail

Excellent communication skills in English

Organizational skills

Adaptability

Self-motivation

Formação académica

Bachelor's degree in life sciences

Bachelor's degree in engineering

Bachelor's degree in biostatistics

Bachelor's degree in programming

Descrição da oferta de emprego

Join to apply for the Clin Ops Delivery Specialist I role at Thermo Fisher Scientific

Work Schedule: Standard (Mon-Fri)

Environmental Conditions: Office

The role involves working highly independently, performing critical assessments in collaboration with study teams or other departments to determine the best approaches to manipulate subject data. The RSM-C is capable of leading active interdepartmental discussions to explore strategies and practices based on trial-specific needs and diverse data sources.

Responsibilities include reviewing subject data from multiple sources with an analytic mindset, identifying trends, risks, and optimization areas, and preparing and analyzing clinical trial datasets. The role requires adapting to ongoing trial developments and providing clear updates to study teams and stakeholders.

The position encourages continuous learning through mentorship, attending presentations, and contributing to departmental documents and policies. The RSM-Central should develop a thorough understanding of protocol schedules, contracts, budgets, and payment terms.

Key responsibilities also involve escalating performance issues, leading internal meetings, managing escalations related to tracking system setup/maintenance, and ensuring data integrity and compliance.

Qualifications and Skills

• Bachelor's degree in life sciences, engineering, biostatistics, programming, or related fields
• Prior clinical research experience (6 months to 1 year) is preferred but not required
• Experience in process development or process improvement (6 months to 1 year) is preferred but not required
• Experience in data assessments, analytics, or critical assessments (6 months to 1 year) is preferred but not required
• Ability to lead multidisciplinary discussions and work independently
• Strong decision-making and documentation skills
• Ability to work under pressure and adapt to changing priorities
• Experience with databases and scientific background is a plus

Skills

• Understanding of database structures and complex data systems
• Proficiency in Microsoft Excel
• Data review and quality control skills
• Attention to detail and problem-solving skills
• Excellent communication skills in English
• Organizational skills for managing multiple tasks
• Adaptability and positive attitude
• Self-motivation and initiative

Additional Information

• Seniority level: Not Applicable
• Employment type: Full-time
• Job function: Research and Science
• Industries: Pharmaceutical Manufacturing and Biotechnology Research