Parexel seeks a Senior Solution Consultant (pharmacovigilance/drug safety) to lead design and delivery of bespoke safety solutions, support pre-award and post-award activities, manage client relationships, and inform strategic direction. Requires a bachelor's in life sciences (or related) and a minimum of 5 years' experience in pharmacovigilance, drug safety services, or clinical research. Position based in India (Mohali/remote) with travel up to 30%.

Parexel Clinical Research Associate II role (China/Beijing, remote) responsible for monitoring investigator sites (SDV), managing site issues, ensuring patient safety and regulatory compliance (ICH-GCP and local laws), maintaining TMF/ELARA and site documentation, training site staff, and producing monitoring reports. Requires a degree in life science/nursing/pharmacy (Bachelor's or above) and at least 1.5 years (2 years preferable) of clinical monitoring/site management experience. Proficient in Chinese and good written and spoken English required.

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.

Senior domain-aligned technical execution leader responsible for orchestrating delivery across Data Ingestion, Data Engineering, and Data Distribution for Real-World Data in life sciences. The role focuses on technical leadership for scalable RWD pipelines, lakehouse design, Azure Databricks, data quality and governance, plus matrixed stakeholder coordination, intake and roadmap management, prioritization, and delivery tracking.

Parexel is hiring a Senior Clinical Research Associate (Core Team) to manage and monitor clinical trial sites (initiation through close-out) for oncology studies. Responsibilities include ensuring protocol adherence, site training and support, CTMS/EDC/TMF maintenance, SAE follow-up, regulatory documentation, audit/inspection readiness, and supply accountability. Role requires at least 4 years CRA experience from Australia or New Zealand and will include remote and on-site visits with extensive travel as required.

The Site Payment Lead manages end-to-end site/investigator payments for assigned studies in a remote capacity (Argentina). Responsibilities include payment setup and modifications, coordinating with project teams and internal stakeholders, ensuring timely and compliant payments, resolving escalations, participating in study start-up and strategy meetings, and producing payment reports. Requires a bachelor's degree, advanced English, and preferred 4+ years' experience in CRO, finance/accounting, or related roles.

Lead planning, coordination, and execution of Clinical Trial Applications (EU CTR and ROW), manage clinical and regulatory documentation, mitigate risks, and coordinate cross-functional global teams. Requires a bachelor's in life sciences/pharmacy and minimum 5 years' industry experience in pharmaceutical/CRO/regulatory submission environments.

Parexel is recruiting an experienced Clinical Project Leader or Senior Project Leader to lead global project delivery for Large Pharma Partnership clients. The role requires demonstrable CRO project leadership across Phase I–III clinical trials, strong financial and client relationship skills, oncology expertise (essential) and familiarity with ICH/GCP and eClinical systems. The position is available remote in specified countries (EMEA and South Africa).

Implements and monitors clinical trials at investigative sites (on-site and remotely), assesses site qualification, conducts source document verification, oversees IP accountability and SAE reporting, completes monitoring documentation, updates trial tracking tools, facilitates audits, mentors junior CRAs, and performs related clinical operations tasks (e.g., protocol amendments, site budget negotiation).

Parexel is hiring a Patient Safety Associate I to support pharmacovigilance operations including ICSR processing, coding, literature monitoring, safety submissions, regulatory database maintenance, and affiliate support. Requires a bachelor’s in life/health sciences or equivalent, foundational drug safety knowledge, and familiarity with safety systems (Veeva Safety preferred). Role is remote within the United States.

Parexel seeks a Senior eClinical Business Lead to support RTSM and DHT study design, requirements analysis, system configuration, integration validation, and UAT across clinical trials. The role requires translating protocol and business requirements into actionable solutions, ensuring regulatory and data-standard compliance (ICH-GCP, CDISC), managing quality and risk, and interfacing with clients and cross-functional teams. Required: bachelor's degree or equivalent and 5+ years building RTSM and/or DHT clinical trial systems.

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.

Parexel is seeking a Senior CRA on an independent contractor basis (6–12 months). Candidates should have ~5+ years CRA experience in Australia (NSW, VIC, SA or QLD preferred). Responsibilities include site management and monitoring (on-site and remote visits), ensuring protocol compliance, CTMS/EDC/TMF maintenance, ICH-GCP and regulatory compliance, SAE follow-up, and participation in audits and investigator meetings. Oncology experience is desirable.

Parexel seeks a Program Lead for FSP Clinical Operations to drive operational excellence, financial performance, and scalable FSP solutions across assigned programs. The role requires leadership of cross-functional teams in a CRO setting, experience with workforce forecasting, billing and financial tracking, and ensuring regulatory-compliant clinical trial operations.

Parexel Consulting (regulatory) is hiring a (Senior) Project Manager to act as client-facing lead for regulatory submission projects (PMDA consultation, CTD support, KOL engagement) from initiation to completion. Responsibilities include scope and budget confirmation, schedule and resource management, coordination of PMDA meetings, vendor and interpreter liaison, training setup, and reporting to an overseas (Europe) manager. English communication skills and project management experience are required; pharmaceutical industry experience is desirable.

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).

Responsible for on-site monitoring including SDV, site management from selection to closeout, training site staff, maintaining TMF/ELARA and SMF, generating monitoring reports, and ensuring compliance with ICH/GCP and local regulations. Requires a degree in life sciences/nursing/pharmacy (or equivalent) and at least 1.5 years (2 years preferable) clinical monitoring/site management experience; proficient in Chinese and good written/spoken English.

Responsible for site monitoring and management including SDV, ensuring studies follow ICH-GCP and local regulations, maintaining TMF/ELARA and SMF, reporting progress and issues, training site staff, and supporting site set-up and closeout. Requires degree in life sciences/nursing/pharmacy, proficiency in Chinese and good written/spoken English, and ~1.5–2 years clinical monitoring/site management experience.

Parexel is seeking a Clinical Research Associate II for its Multi-Sponsor Clinical Trials Team in Poland (remote). The role includes conducting site qualification, initiation, monitoring and termination visits; ensuring patient safety, protocol and regulatory compliance; overseeing data quality and drug accountability; and supporting patient recruitment. Requires site management/clinical research experience, ability to perform monitoring independently, a bachelor’s degree in a life/health science, and proficiency with CTMS/EDMS and MS Office.

Parexel is hiring an Investigator Contract Lead (FSP) responsible for standard site contracting (CSA/CRC/ICD review & execution), site budget development aligned with Fair Market Value principles, basic legal/cost negotiation with sites, and coordination with CTM/Legal/study teams. Requires legal background, preferably an MS degree, and more than 3 years' clinical trial site contracting experience; strong communication, writing and PowerPoint skills are requested.