Thermo Fisher Hiring Centralized Monitoring Analyst (Level I & II)

Thermo Fisher Scientific Recruitment – Centralized Monitoring Analyst (Level I & II)

Thermo Fisher Scientific is hiring for the Centralized Monitoring Analyst (Level I & II) position within its clinical research services team. This opportunity is associated with the company’s PPD clinical research portfolio and focuses on reviewing clinical trial data, identifying trends, and supporting risk-based centralized monitoring activities. Candidates with experience in clinical monitoring, clinical data management, biostatistics, or related clinical trial functions may be suitable for this role. Applicants should have a relevant degree or equivalent qualification and approximately two or more years of comparable experience.

Company Overview

Thermo Fisher Scientific provides scientific services and solutions, including clinical research services through its PPD clinical research business. The clinical research team supports the development of medicines and therapies by helping pharmaceutical and biotechnology companies conduct clinical trials.

Job Details

Job Role & Responsibilities

The Centralized Monitoring Analyst reviews clinical trial data and identifies issues, trends, signals, and potential risks that may require follow-up by project teams.

Key responsibilities include:

• Review clinical trial data using various tools and systems in accordance with the centralized monitoring plan, with support from senior team members.

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

• Ensure that review results are documented appropriately according to departmental procedures.

• Participate in the development of risk characterization and reporting, where required.

• Support review setup activities, including updating departmental databases and generating reports.

• Analyze operational and patient clinical trial data to identify trends and potential concerns.

• Communicate identified issues and potential risks to project team members for follow-up action.

Eligibility & Qualifications

Candidates should meet the following educational requirements:

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Microbiology, M.Sc. Microbiology, Statistics, Biostatistics, or related clinical research qualifications. These are examples of potentially relevant courses; the official posting specifies a bachelor’s degree or equivalent qualification rather than an exhaustive list of accepted degrees.

• Bachelor’s degree or equivalent, along with a relevant formal academic or vocational qualification.

• Previous experience providing the knowledge, skills, and abilities required for the role, comparable to 2+ years.

• Prior experience in clinical monitoring, data management, biostatistics, or a related field supporting clinical trials is preferred.

An equivalent combination of appropriate education, training, and directly related experience may also be considered.

Knowledge & Skills Required

Applicants should demonstrate the following skills and knowledge:

• Ability to apply fundamental knowledge while following regulatory guidelines, global standard operating procedures (SOPs), and client expectations.

• Strong attention to detail and numerical accuracy.

• Analytical thinking, problem-solving skills, and sound judgment.

• Ability to work productively under direct supervision.

• Ability to maintain confidentiality of clinical data and clients’ proprietary information.

• Flexibility and adaptability when project requirements change.

• Ability to work independently and collaboratively within a team.

• Good written and verbal English communication skills.

• Computer proficiency, including Microsoft Word, Excel, and PowerPoint.

• Ability to extract relevant information from study documentation, protocols, and electronic clinical study data systems.

• Ability to identify trends in site and study data.

• Workload prioritization and planning skills to manage changing project demands.

• Understanding of project protocols, centralized monitoring plans, and other functional plans.

• Broad knowledge of clinical trial roles, functions, and processes.

• Understanding of medical and therapeutic areas and medical terminology.

Work Schedule & Environment

The position is listed with a second-shift afternoon schedule and an office work environment. The job page also categorizes the role as remote/hybrid, so candidates should review the official listing for the applicable work arrangement at their location.

The description mentions possible exposure to biological fluids and infectious organisms in clinical or laboratory environments, as well as electrical office equipment. Personal protective equipment, including protective eyewear, garments, and gloves, may be required depending on the working environment.

How to Apply

Interested candidates can review the complete job description and submit their applications through the official Thermo Fisher Scientific careers portal.

Apply here: Centralized Monitoring Analyst (Level I & II) – Official Job Posting

Review the official listing for the latest application status, location-specific requirements, and employment details.

Job Summary