Hands-on Senior Power Apps Developer (6+ years) experienced in model-driven and canvas Power Apps, Power Automate, Power BI, Power Pages, Power Query and SharePoint. Responsibilities include designing, coding, testing and documenting solutions, providing architecture/configuration/administration for Microsoft 365 technologies, customizing SharePoint lists, and working with business stakeholders. Experience in clinical research is desired.

Parexel seeks a Senior Clinical Research Associate to perform onsite and remote site monitoring, manage site activation through database lock, ensure protocol compliance and patient safety, support enrollment and investigator interactions, maintain TMF and trial documentation, and mentor junior staff. Role is remote for candidates based in Istanbul or Ankara and requires willingness to travel ~60–80% within the region; fluency in English and Turkish is required.

Director-level individual contributor who serves as primary technology advisor for strategic client accounts. Responsibilities include building senior client relationships, defining account-level technology strategies and roadmaps, facilitating cross-functional collaboration, supporting commercial proposals and contract alignment, enabling delivery and escalation management, and mentoring related roles. Requires 10+ years in client-facing technology or consulting roles; experience in regulated or life-sciences environments and knowledge of SDLC, validation, and enterprise integrations preferred. Role is remote from multiple Indian cities.

Responsible for end-to-end proposal development and strategy: collaborating with proposal managers, sales leaders and cross-functional teams; conducting market and therapeutic-area research; maintaining proposal and contract templates; contributing to case studies and thought leadership; and mentoring junior team members. Role is homebased and supports business development for a CRO across multinational environments.

Senior/Vice President Technical on the Regulatory Science team providing high-level regulatory and clinical consulting across the product lifecycle. Responsibilities include leading teams of subject-matter experts, managing client engagements, authoring clinical regulatory materials, advising clients to health authorities, mentoring staff, and contributing thought leadership. MD or PhD required; 15+ years' experience in clinical development/clinical trial design and regulatory submissions; prior regulatory agency medical review experience preferred. Preferred therapeutic experience: neuroscience, rare disease, immunology, endocrinology/metabolism. Role is home-based (United States) with travel up to 20–30%.

Lead FSP Clinical Operations activities including program and line management, resourcing and staff development, client governance, KPI and financial tracking, escalation/CAPA management, and cross-functional collaboration. Requires minimum 5 years FSP Clinical Operations experience, 3 years line management experience, remote work capability, and proficiency in English.

Parexel seeks Project Leader and Senior Project Leader candidates to lead global biotech clinical trials (Oncology/Hematology, Respiratory/General Medicine, Obesity/Endocrine). Responsibilities include providing leadership to project teams, managing day-to-day operations, scheduling, resources and budgets, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Undergraduate degree in a clinical/health field required (advanced degree preferred); minimum 2+ years' experience leading global clinical trials in a CRO, biotech, or pharma environment.

Responsible for implementing eClinical technology for studies, including requirements gathering, design, configuration and integrations; primary contact for study technology with internal teams and external clients. Requires clinical trials experience, familiarity with CTMS/EDMS/EDC/IVRS, knowledge of CDISC SDTM, ICH-GCP and 21 CFR Part 11, and strong project/client management and communication skills.

Role leads eClinical technology implementation for studies (design, requirements gathering, documentation, configuration, integrations and delivery). Position is available in Romania, Poland, Serbia and South Africa and supports remote/home-based working. Requires proven clinical trials experience, knowledge of eClinical systems (CTMS/EDMS/EDC/IVRS), regulatory standards (ICH-GCP, 21 CFR Part 11) and familiarity with CDISC SDTM.

Client-dedicated Regulatory Affairs Consultant responsible for strengthening global regulatory compliance and quality operations across GxP environments. Key responsibilities include controlled document management and governance, training governance and compliance, inspection readiness (FDA, EMA, MHRA and other authorities), QMS process management (deviations, CAPA, change control, SOPs) and supporting remediation and continuous improvement. Requires 8+ years in regulatory compliance/QA in pharma/biotech and experience with eDMS/Veeva Vault; fluent English.

Senior RWE/RWA Analyst Programmer (remote) responsible for designing and coding R and SQL programs, cleaning and validating real-world data from sources such as Optum and Flatiron, implementing analyses per RWE protocols, and developing dashboards/reports. Requires an MS in a related field, at least 7 years of RWD/RWE experience, fluency in R and SQL, and familiarity with healthcare coding systems; SAS/Python experience is advantageous.

Role involves validating, maintaining, and submitting regulatory data for medicinal products in compliance with EMA guidelines, including xEVMPD submissions and PLM activities. Requires hands-on experience with Veeva Vault RIM, RIMS/DMS, preparation of EMA deliverables (eAF, eSMP), and management of SmPC/PIL and post-marketing activities.

Parexel seeks a Clinical Research Associate I-II to monitor clinical trial sites (initiation through close-out). The role requires minimum 1 year of independent CRA monitoring experience in Australia or New Zealand and involves site management, ensuring ICH-GCP and regulatory compliance, TMF/document management, use of CTMS/EDC/EDMS/IVRS/SIS systems, SAE and CRF follow-up, site training, and frequent travel. Degree or equivalent health/nursing qualification preferred.

The Site and Monitoring Health Lead (US, remote) applies ICH-GCP and monitoring experience to oversee CRO monitoring effectiveness, perform risk-based site and study oversight (including SSOPs and Sponsor Oversight Visits), support inspection preparation, analyze trends and root causes, and work with cross-functional teams and investigators to maintain study quality. Lead CRA experience and proficiency in English required; moderate travel expected.

Parexel is recruiting a Clinical Trial Leader to lead planning, implementation and delivery of international clinical trials, dedicated to a single sponsor. The CTL is accountable for trial timelines, feasibility, patient/site engagement, vendor management, adherence to GCP and regulatory requirements, risk mitigation, recruitment monitoring, budget and safety oversight, and timely trial closeout. Role requests strong clinical trial project management experience, degree qualified (Master’s preferred), and oncology experience (or experience in CNS, Immunology or Vaccines).

The Regulatory Submission Coordinator (Associate/Sr Associate) supports preparation, coordination, and delivery of regulatory submissions and labeling activities for biological products across assigned LATAM countries. Responsibilities include managing submission documentation (e.g., non-eCTD/Module 1), maintaining regulatory systems (Veeva RIM, DocNet, Apollo), coordinating labeling and mock-ups, and supporting inspection readiness. Mandatory: experience with biological products, regulatory submission processes in LATAM, Veeva RIM/document management tools, and effective written/verbal English and Spanish. Based in Mexico or Argentina.

Parexel is hiring a UK-based, home-based Global Clinical Trial Leader (CTL) accountable for setup, execution and delivery of assigned trials. Responsibilities include trial planning and feasibility, oversight of trial preparation and conduct, risk mitigation, vendor oversight, budget oversight, TMF archiving, data delivery, and support for safety reporting, SMC/DMC and medical writing. Requires a minimum of 5 years' relevant clinical trial management experience and experience in Oncology, CNS, Immunology or Vaccines.

Responsible for creating placeholders, uploading MLR content and reference documents, linking and anchoring assets, initiating and monitoring QC workflows in Veeva Vault PromoMats/Medical, and coordinating with internal and external stakeholders to ensure asset quality. Role prefers candidates with scientific/medical or data analysis background and prior Veeva or pharmaceutical content review experience.

Parexel seeks a Senior Customer Strategy Analyst for the Customer Access Strategy team to support proposal development, budgeting/WBS, account strategies, market access research (including use of Citeline and Data monitor), and tracking of new business and contracting. Requires a Bachelor's degree (advanced preferred), 4+ years in market access or life sciences consultancy/agency/CRO, strong desk research and proposal skills, and fluent written and verbal English.

Parexel is hiring a Senior Physician for Patient Safety to perform ICSR medical review, assess causality and seriousness, assign MedDRA codes, write case narratives, and support regulatory reporting. Requires MBBS or MD, completion of basic clinical training, and a minimum of 2 years' experience in ICSR medical review; responsibilities include liaising with stakeholders, supporting audits/inspections, mentoring junior physicians, and contributing to process improvements.