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.

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.

The Clinical Laboratory Study Manager supports precision medicine studies by managing biosample process planning (collection, storage, shipping, destruction), vendor selection and oversight, sample tracking and LIMS activities, and coordination with data management/biostatistics for data transfer and reporting. Requires a bachelor's degree (life sciences preferred) and a minimum of 6 years clinical research experience; programming skills (Python/R/Perl/SQL) and regulatory knowledge (ICH/GCP, FDA) are referenced when acting in programming or technical lead capacities.

Remote Senior PK Analyst role (based in listed countries) requiring 4+ years' programming experience in R and SAS to derive PK/PD parameters, program and validate NONMEM and derived datasets, and produce tables/listings/figures/statistical appendices. Role involves working to SOP/ICH/GCP standards, mentoring junior analysts, and contributing to process and quality improvements.

Role involves deriving PK/PD parameters, programming and validating NONMEM datasets and PK/PD-derived datasets, producing and validating tables/listings/figures and statistical appendices, following SOPs/ICH/GCP, mentoring junior analysts, and participating in process improvement. Requires 4-6 years' relevant experience and expert SAS and/or R skills; experience with Phoenix WinNonlin and knowledge of pharmacokinetic data and regulatory standards.

Parexel is hiring a Senior Statistical Programmer to support clinical trial analysis and reporting for a single sponsor. Responsibilities include producing and QCing derived datasets (SDTM, ADaM), TFLs, dataset specifications, reviewing SAPs and mock-shells, leading/coordination of programming teams, and project management (timelines, budgets, resourcing). Requires proficiency in SAS, knowledge of CDISC standards, experience with tools such as Pinnacle 21 and XML, a Bachelor's degree in a relevant field, and a minimum of 3 years' clinical/statistical programming experience. Remote work is supported; applicants must be authorized to work in South Africa and Parexel will not sponsor visas.

The Data Surveillance Analyst conducts data and operational reviews per project Data Surveillance Plans, helps develop DSPs (KRIs, QTLs, statistical parameters), configures surveillance technologies (e.g., CluePoints), documents findings and issues, and supports central monitoring reporting. Requires a university degree (medical/biological/pharmacy/data analytics), fluent English, hands-on experience with SAS/R/SQL, knowledge of RBQM and centralized/data-driven monitoring, and familiarity with CTMS/EDMS and SDTM concepts.

Parexel is hiring a home-based Data Surveillance Analyst for selected EMEA locations (Croatia, Hungary, Czech Republic, Lithuania, Poland, Serbia, Romania) and South Africa (Bloemfontein). The role involves developing Data Surveillance Plans (KRIs, QTLs, central statistical analysis), configuring and maintaining surveillance technologies (e.g., CluePoints), performing data reviews, documenting findings, and supporting meetings and audits. Requirements include a university degree (medical/biological/pharmacy/data analytics), fluent English, and hands-on experience with SAS, R, and/or SQL; experience with RBQM, centralized monitoring, CTMS/EDMS, and basic SDTM knowledge is also noted.

The Health Economics Associate will support development and adaptation of health economic models for country-specific reimbursement submissions, perform data analysis and model validation, conduct literature and HTA guidance searches, and assist with documentation and quality assurance. Required: a master’s degree in a quantitative or life science discipline and strong Excel skills (including macros/VBA).

Parexel seeks a Statistical Programmer II to produce and QC derived clinical trial datasets, tables, figures, and listings using SAS (including SDTM and ADaM). The role requires adherence to SOPs and regulations (ICH-GCP, 21 CFR Part 11), participation in project start-up and documentation, and providing training/mentorship as appropriate. Competent written and oral English and a relevant degree or equivalent experience are required.

Parexel seeks a Senior Associate with a Master's/PhD and at least 3 years' experience in pharma, consultancy, HTA/access, or academia. The role involves designing evidence-generation plans, conducting statistical analyses (e.g., GLMs, survival analysis, NMA, Bayesian methods), developing technical documentation and economic models, and contributing to cross-functional Access/HTA strategies. Proficiency in R and GitLab is required; familiarity with SAS, Python, WinBUGS, or JAGS is a plus.