Seeking a Regulatory Affairs Consultant to develop, review and manage regulatory submissions and compliance activities for pharmaceutical products in Switzerland (clinical through post-market). Role requires strong knowledge of Swissmedic regulations, experience with CTD/eCTD submissions, labeling (SmPC/PIL), CMC variations, and 5+ years' regulatory affairs experience. Fluency in German, French and English is required.

Parexel seeks a Clinical Research Associate with at least 12 months of direct onsite monitoring experience to manage clinical sites through qualification, initiation, monitoring, and closeout. The role involves ensuring study quality, participant safety, regulatory compliance, data integrity, and supporting enrollment across therapeutic areas. Experience with CTMS/EDMS and GCP is required; oncology, ophthalmology, CAR-T, or MASH experience is preferred.

Provides recruitment and engagement support to clinical trial site staff in Mexico (remote). Responsibilities include coordinating site credentials and training materials, monitoring and following up on referrals, maintaining site tracking information, escalating issues, contributing to study-level updates, and performing related administrative tasks. Requires a BA/BS (or equivalent), basic clinical research knowledge, minimal recruitment/retention experience, strong communication and organizational skills, and proficiency with Microsoft Office and database applications.

Parexel is hiring an Initiation Clinical Research Associate (iCRA) for Latin America (Brazil, Argentina, Mexico). The role is home-based and focuses on study start-up and site activation activities, regulatory submissions and approvals, eTMF/CTMS documentation, and ensuring sites remain audit-ready. Requires strong clinical research and study start-up experience, knowledge of ICH-GCP and clinical trial systems, and excellent written and oral English.

Parexel seeks a Clinical Data Associate II (remote, South Africa) to perform clinical data management activities across Phase I-IV studies, including EDC coordination (Rave preferred), eCRF design, query management, data reconciliation, database lock support, and vendor/CRO oversight. Requires a bachelor's in a scientific/healthcare field and at least 2 years' data management experience; knowledge of CDISC, ICH/FDA guidances, GCDMP, 21 CFR Part 11, MedDRA, and WHO drug dictionaries.

Parexel seeks a Senior Clinical Data Associate in South Africa (remote) to lead and support data management activities for Phase I–IV clinical trials. Responsibilities include EDC system coordination (RAVE preferred), eCRF design and annotated CRFs, query management, reconciliations, database migrations/upgrades, UAT, and supporting database lock and inspection readiness. Requires a scientific degree and at least five years' data management experience in pharma/biotech; knowledge of CDISC, GCDMP, 21 CFR Part 11, MedDRA, and WHO drug dictionaries.

The Programming Lead will manage and optimize biomarker sample handling, kit logistics, laboratory data and associated programming across clinical studies. Responsibilities include developing tracking tools and dashboards, collaborating with data management and biostatistics, overseeing laboratory databases and vendor activities, and ensuring compliance with clinical and regulatory standards. Requires a life sciences degree, at least 6 years' clinical research experience, and proficiency in Python/R/Perl/SQL and related technologies.

Parexel seeks a Statistical Programmer I (Intern) to perform SAS-based statistical programming for clinical studies, producing low-to-medium complexity derived datasets (SDTM, ADaM), tables, figures and listings. Responsibilities include maintaining study documentation per SOPs, following ICH-GCP and applicable regulations (e.g. 21 CFR Part 11), and participating in audits. Role requires degree-level education or equivalent experience and competency in written and oral English. Location indicated as Bloemfontein, South Africa (remote).

Parexel is hiring Project Leader and Senior Project Leader roles (home-based, United States) to lead global clinical trials for biotech clients across therapeutic areas including neurology, oncology, respiratory, dermatology, cardiology and GLP-1/obesity. Requires at least 2 years' experience leading global clinical trials (project management within CRO/biotech/pharma preferred) and experience in project scheduling, resource and budget management, team coordination and the full clinical development process through regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader candidates to provide leadership for global clinical trial projects across therapeutic areas. Roles are homebased (United States - Remote) and require a minimum of 2+ years' experience leading global clinical trials in project management within a CRO, biotech, or pharma, plus experience in project scheduling, resource and budget management, team coordination, and the clinical development process through regulatory submissions.

Parexel is hiring a Regulatory Affairs professional to prepare, compile, review, and submit regulatory applications to INVIMA (new registrations, variations, renewals, supplements, amendments, and responses), manage product lifecycle activities for Colombia, coordinate cross-functional dossier contributions, maintain submission trackers and schedules, monitor regulatory developments, and collaborate with regional/global stakeholders. Requires minimum 5 years' regulatory experience in the pharmaceutical/biotech industry and proven experience with Colombian regulatory requirements.

Parexel is hiring a Vendor Strategy Director / Project Director to define and execute program-level vendor strategies across clinical trials. The role partners with clinical program leads, procurement and cross-functional stakeholders to manage supplier performance, mitigate risks, support inspection readiness, enable early supplier engagement, and drive operational improvements. Requires 10+ years' industry experience and fluency in English.

Role provides coordination and administration across study start-up, execution and closeout; manages local eTMF/ISF and document tracking per ICH-GCP; supports EC/IRB and regulatory submissions, site-level contract/payment activities, meeting preparation, and liaison with internal/external stakeholders.

Parexel is hiring a Senior Data Engineer to design, develop, and support ETL programs and data integration solutions in Databricks and Azure (Azure SQL, Azure Data Factory). The role includes architecting software and product extensions, mentoring engineers, producing technical and architectural documentation, and supporting deployments using Azure DevOps Git in a clinical trials context.

Parexel is recruiting a Senior Medical Director. The role references clinical development solutions including clinical trials, regulatory, consulting and market access. The posting lists location as China (Shanghai) with remote.

Lead role responsible for sample management, biosample processing, data acquisition and programming (Python/R/SQL), LIMS and clinical trial logistics for precision medicine studies. Requires minimum 6 years clinical research experience and a bachelor's degree in life sciences or equivalent.

Programming Lead supporting sample management, biosample processing, kit logistics, LIMS and related data operations across the study lifecycle. Role includes collaborating with study teams, data management and biostatistics on data capture and transfer, vendor assessment and operational budgeting, and developing tools/dashboards and programming solutions (e.g., Python/R/SQL) to track samples, kits and laboratory data. Requires a minimum of 6 years clinical research experience and fluent English.

Role provides regulatory strategy and end-to-end management of submissions, registrations, post-approval changes and CMC activities for biologics across LATAM (Peru, Argentina, Brazil, Mexico). Requires 5+ years in the pharmaceutical industry, mandatory experience with biological products, strong CTD and dossier preparation skills, and proficiency in English and Spanish.

Responsible for coordinating clinical project teams on small to midsize studies, managing study start-up activities, monitoring timelines, patient recruitment and data cleaning, and resolving site issues. Ensures compliance with ICH-GCP, local regulations, and Parexel SOPs; prepares for audits/inspections and supports database lock, close-out, and archiving. Requires substantial clinical research experience (e.g., CRA), strong English communication, proficiency with Microsoft Office and WebEx, and ability to travel as required.

Parexel FSP seeks a Clinical Laboratory Study Manager based in Argentina to oversee biosample planning, storage, shipping, tracking, vendor management, and related data operations for precision medicine studies. The role partners with clinical, data management and biostatistics teams to develop sample-related protocol sections, manage LIMS and specialty lab databases, ensure regulatory compliance (ICH/GCP/US FDA), and may involve programming work (Python/R/SQL) and logistics oversight. Minimum 6 years clinical research experience and a life sciences bachelor degree or equivalent are required.