Non-Interventional Study Research Manager

Parexel

Non-Interventional Study Research Manager at Parexel managing observational research studies and leading operational activities for clinical trials in Mexico and Brazil.

Posted 7/24/2026full-timeRemote • 🇲🇽 MexicoJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading operational activities for observational research studies, including study planning, execution, and compliance with GPP and SOPs. Proficient in project management, communication, and collaboration within clinical research environments, particularly in oncology.

Highest-signal resume keywords

Oncology ExperienceClinical Research ManagementProject ManagementEpidemiologic Research KnowledgeFluency in English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study PlanningStudy ExecutionData CollectionChart ReviewDatabase ManagementMolecular EpidemiologyProtocol PreparationLiterature Review Abstraction

Soft Skills

Excellent CommunicationInterpersonal SkillsPrioritization Skills

Certifications & Qualifications

Bachelor's Degree in Public Health or Science Discipline

Industry Keywords

Observational ResearchGPP ComplianceSOPsPrimary Data CollectionOutcomes Research

About the role

Key responsibilities & impact

Leads operational activities related to study planning, study execution, and the summarization of results from observational research studies
Coordinates the end-to-end process for executing observational or non-interventional research studies in compliance with GPP and SOPs
Plans, initiates, executes, and closes out primary data collection, chart review, database, and molecular epidemiology studies
Collaborates with colleagues in GMSA to support lead scientists in overall operational support for study conduct
Provides study-level management support including the execution of appropriate services for approved proposals/scopes of work
Participates in protocol and interim/final report preparation and literature review abstraction

Requirements

What you’ll need

Two or more years of work experience within clinical/observational research or equivalent experience
Oncology experience is required
Excellent communication and interpersonal skills
Basic knowledge of epidemiologic or outcomes research
Fluency in English (written and spoken)
Strong project management and prioritization skills
Bachelor's degree in public health or science discipline

Benefits

Comp & perks

Professional development opportunities
Flexible working arrangements