Clin Ops Delivery Specialist I

Thermo Fisher Scientific Inc.; São Paulo; Presencial; BRL 30.000 - 70.000; Tempo integral

Resumo da oferta

An established industry player is seeking a highly independent professional to join their dynamic team. In this role, you will lead critical assessments and collaborate with study teams to optimize subject data manipulation strategies. Your expertise in data analysis and communication will be vital in reviewing clinical trial datasets and identifying trends, risks, and areas for improvement. This position offers an exciting opportunity to enhance your skills in a fast-paced environment while contributing to impactful clinical research projects. If you thrive under pressure and enjoy tackling challenges, this role is perfect for you.

Qualificações

• Bachelor's degree in life sciences or related fields is required.
• Prior experience in clinical research or data analytics is desired.

Responsabilidades

• Lead discussions on data manipulation and optimization strategies.
• Review and analyze clinical trial datasets for trends and risks.
• Provide updates to study teams on subject data statuses.

Conhecimentos

Database structure understanding

Microsoft Excel proficiency

Data capturing and reviewing

Quality control support

Attention to detail

Problem-solving skills

Written and verbal communication

Organizational skills

Adaptability to changing priorities

Self-motivation

Formação académica

Bachelor's degree in life science-related fields

Engineering

Biostatistics

Programming

Descrição da oferta de emprego

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Works highly independently and performs 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 and challenging interdepartmental discussions to explore best strategies and practices after understanding trial-specific needs and diverse databases that can be used as sources of information.

Reviews subject data from multiple sources with a data analytic mindset, capable of identifying trends, risks, gaps, and areas for optimization as the subject data and the trial develop. Prepares and analyzes clinical trial patient datasets. Adapts to constant changes as the trial develops. Capable of providing concise and clear updates to study teams and other key stakeholders after processing and reviewing subject data.

Continually makes efforts to increase knowledge base and professional skills in areas such as programming, technology and techniques, clinical trials, and the pharmaceutical industry by working closely with mentors, attending presentation/teaching events, and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles.

The RSM-Central generates a thorough understanding of protocol schedule of events (visits, activities, and procedures), contracts, budgets, and/or payment terms.

Escalates performance issues to clinical, site payments, and IT managers and may assist with resolution (follows escalation pathway as applicable). Leads internal team meetings and provides updates on subject data statuses. Manages escalations (project team, site, and sponsor) regarding tracking system setup/maintenance issues.

Qualifications and Skills (some of the below are desired):

• Bachelor's degree in life science-related fields, Engineering, Biostatistics, and/or Programming or related fields/degrees
• If possible (but not required), prior clinical research experience or related fields of minimum 6 months to 1 year or related experience involving knowledge of clinical trials.
• If possible (but not required), prior experience of minimum 6 months to 1 year on process development or process improvement.
• If possible (but not required), prior experience of minimum 6 months to 1 year on data assessments, analytics, or critical assessments.
• Highly independent and capable of leading multidisciplinary discussions as needed.
• Comfortable with decision making and proper documentation practices.
• Capable of working under continuous pressure and continuously changing challenges adapting to new priorities and needs as they arise.
• If possible (but not required), experience with databases with a scientific background.

Skills

• Understanding of database structure and complex data systems
• Proven understanding and use of Microsoft Excel
• Capable of effectively capturing and reviewing data
• Capable of providing quality control support
• Good attention to detail
• Good problem-solving skills
• Excellent written and verbal communications skills to effectively interface with teams, including proficiency in the English language
• Capable of effectively organizing and managing multiple assignments with challenging timelines
• Capable of adapting and adjusting to changing priorities
• Positive attitude and the ability to work well with others
• Demonstrate initiative and self-motivation