Sr. Centralized Monitoring Analyst I

Thermo Fisher Scientific Inc.; México; A distancia; USD 30,000 - 45,000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific Inc. is seeking a Sr CM Analyst I to lead centralized monitoring efforts in clinical research. The role involves developing monitoring plans, managing timelines, and ensuring data integrity to advance global health initiatives. Applicants should possess a Bachelor's degree and at least 5 years of relevant experience in clinical trials.

Formación

• Bachelor's degree or equivalent relevant qualification.
• Minimum 5 years' experience in clinical monitoring or related field.

Responsabilidades

• Lead Centralized Monitoring functional activities and develop monitoring plans.
• Generate reports, support budget management, and communicate with study team.
• Train and mentor junior team members.

Conocimientos

Analytical skills

Attention to detail

Problem-solving abilities

Organizational skills

Communication skills

Educación

Bachelor's degree or equivalent

Herramientas

MS Office

Interactive computer systems

Descripción del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific Inc., our mission is to make the world healthier, cleaner, and safer. As a Sr CM Analyst I, you will play a pivotal role in advancing global health initiatives through world-class clinical research. Our collaborative environment, dedication to excellence, and brand-new resources will empower you to excel and make a global impact.

Centralized Monitoring (CM) is an integral part of PPD’s risk-based quality management (RBQM) strategy. We deliver risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data. Ongoing data assessments from our Centralized Monitoring group facilitates dynamic adaptation of monitoring plans with a focus on critical-to-quality risks that drive data quality and have the greatest impact on data integrity and subject safety.

Job Responsibilities

·Serve as the Centralized Monitoring functional lead, with knowledge in RBQM methodologies, tools, and processes.

·Lead activities such as developing centralized monitoring plans and generating findings reports.

·Manage review timelines and support budget management.

·Serve as functional representative, communicating and working with the study team.

·Ensure reviews are complete, generate reports, and lead Centralized Monitoring Review meetings to discuss issues and risks with the study team.

·Contribute to risk assessment through department risk assessment tools and participate in cross-functional risk assessment review meetings.

·Characterize and track evidence of issues, signals, and potential risks.

·Provide training and mentorship to junior team members.

Education and Experience

·Bachelor's degree or equivalent relevant formal academic/vocational qualification.

·At least 5 years of experience in clinical monitoring, data management, biostatistics, or a related field in support of clinical trials.

·Equivalent combinations of education, training, and/or directly related experience will be considered.

Knowledge, Skills and Abilities

·Strong organizational skills with adherence to regulatory guidelines and global SOPs.

·Outstanding attention to detail and numerical skills.

·Proven analytical and problem-solving abilities.

·Ability to work independently and within a team environment.

·Solid oral and written communication skills.

·Proficiency with MS Office and interactive computer systems.

·Ability to extract pertinent information from standard study documentation.

Working Environment

Thermo Fisher Scientific values the health and well-being of our employees and encourages a balanced environment. You must be able to:

·Communicate effectively with diverse groups.

·Work upright, stationary, and/or standing for typical working hours.

·Lift and move objects up to 25 pounds.

·Work in non-traditional environments.

·Use and learn standard office equipment and technology proficiently.

·Perform under pressure while prioritizing multiple projects.