Implements and monitors clinical trials per ICH GCP and local regulations. Responsibilities include site qualification and initiation, source data verification, IP accountability, SAE verification, essential document reconciliation, audit facilitation, mentoring junior CRAs, and supporting protocol amendments and investigator site budget negotiations. Role involves on-site and remote monitoring; location indicated as Wuhan/Chengdu, China.

The Data Surveillance Analyst will develop and support Data Surveillance Plans, configure and maintain surveillance technologies, review clinical and operational data to identify trends/outliers/risks, document findings, present results to study teams and clients, and support close-out activities. Requires degree (medical/biological/pharmacy/data analytics preferred), fluent English, minimum 3 years' relevant CRO/pharma experience, and basic SAS or SQL (or other programming) with data analytics experience. Compliance with ICH-GCP and experience with centralized/adaptive monitoring is expected.

Homebased role in Poland on a 6-month fixed-term contract supporting clinical trials by drafting and negotiating clinical study agreements, service and team member agreements; managing full contract lifecycle; ensuring ICH-GCP and local law compliance; liaising with sites and internal stakeholders; tracking progress and driving process improvements. Bachelor's degree in law, economics, business, social sciences or related field; fluency in English and local language; proficiency in MS Office. No prior industry experience required.

The role provides technical expertise for IRT vendors from study start-up to closeout, including protocol and study specification review, vendor selection support, contract and budget review, invoice reconciliation, risk/contingency planning, UAT, training support, and ensuring GxP/ICH compliance. Requires 3+ years' clinical operations/IRT vendor management experience and a bachelor's degree (or equivalent).

Associate Director responsible for defining and executing enterprise Quality Engineering strategy, modernising testing and automation practices, leading global QE delivery (including vendors/offshore), ensuring regulatory and GxP-aligned QA, and driving governance, tooling and metrics to improve product quality and inspection readiness. Role is UK-based and can be fully home-based/remote within the UK.

Lead enterprise-wide quality compliance, governance, operational process excellence, vendor governance and risk management across Parexel's global Data & Technology organisation. Responsibilities include QMS and SOP ownership, SDLC governance, third-party and cloud vendor oversight, audit and inspection readiness, risk framework development, and cross-functional leadership with Quality, Regulatory, Clinical and Security stakeholders.

Parexel is recruiting a Clinical Research Associate I/II based in Chengdu (remote option). Responsibilities include on-site and remote monitoring, site initiation/qualification, regulatory document management, updating CTMS/TMF/EDC, ensuring ICH-GCP compliance, addressing site issues, and supporting recruitment and training. Candidate should have site management or equivalent clinical research experience and a degree or relevant nursing qualification.

Lead development of data-driven feasibility strategies to identify countries, sites, and patient populations; perform risk-based feasibility analyses and recommend mitigation approaches; partner with patient recruitment and site alliance teams to create integrated strategies. Create high-quality proposal content, present strategic approaches in bid pursuits, collaborate cross-functionally, drive innovation in feasibility processes and contribute to therapy area strategy. Advanced degree preferred; role requires several years of experience in the pharmaceutical or CRO industry with expertise in clinical trial feasibility, project management, or clinical operations.

Associate-level role contributing statistical capabilities and methodological support across project stages under supervision. Responsibilities include design and delivery of client solutions, sample size/power calculations, drafting statistical protocol sections, developing statistical analysis plans and programs, QC of outputs, and providing statistical input to clinical study reports. Requires a master's or higher in a quantitative field, strong foundation in statistical methods, and proficiency in statistical programming (e.g., R, SAS, Python, SQL).

Responsible for design and writing of trial outlines, protocols and amendments in collaboration with internal and external experts; create and deliver clinical/protocol training; establish and oversee Data Monitoring Committees and endpoint adjudication committees; maintain direct contact with investigative sites to support enrollment and address protocol questions. Requires project management/leadership experience, knowledge of GCP and regulatory requirements, and fluency in English and the host country language.

Parexel is hiring a junior Site Contracts Associate (home-based) to draft, negotiate, and manage site and service agreements for clinical trials across Croatia, Czech Republic, Hungary, Romania, and Serbia. Responsibilities include ensuring ICH-GCP and local law compliance, managing the full contract lifecycle, liaising with internal and external stakeholders, identifying risks, and driving process improvements. Bachelor’s degree required; no prior industry experience necessary. Proficiency in Italian and English and MS Office required.

Parexel is hiring a Site Contracts Associate (entry level) to draft, negotiate, and manage site agreements and related documents for clinical trials. Responsibilities include ensuring compliance with ICH-GCP and local laws, interpreting site feedback, managing the contract lifecycle, communicating with internal and external stakeholders, identifying risks, and driving process improvements. Required: bachelor's degree in a related field, fluency in English and Spanish, strong negotiation and communication skills, and proficiency in MS Office. Role is remote but candidates must reside in Croatia, Czech Republic, Hungary, Romania, or Serbia.

Senior Regulatory Affairs Consultant (CMC Biologics) role requiring demonstrated experience (10–14 years) in new registrations, lifecycle maintenance and renewals for biologics (vaccines, recombinant proteins, mAbs, plasma-derived therapies). Responsibilities include preparation/authoring and review of global and regional regulatory submissions (MAAs, variations) across US, EU, Japan, Canada, Switzerland and Australia; team lead duties to guide and mentor technical staff. Minimum bachelor’s degree in a scientific/technical discipline; advanced degree preferred.

Senior Power Platform Engineer responsible for spearheading Microsoft Copilot and Azure AI implementations across enterprise applications, developing low-code solutions using Power Apps/Power Automate/Power BI/Power Pages, integrating SharePoint and Microsoft 365 content, and leveraging Azure AI services (Cognitive Services, ML, Bot Services). Requires 6+ years' software development experience and experience with Agile.

Parexel is recruiting a home-based Senior Clinical Research Associate (Spain) dedicated to oncology studies under an FSP model. The role includes full site management and supervisory monitoring activities, mentoring junior CRAs, and working with sponsor teams and technology. Requires minimum 4 years' experience in oncology site monitoring and independent site monitoring, plus knowledge of clinical trial methodology, GCP/ICH, and applicable clinical research legislation.

Parexel seeks a Senior Clinical Research Associate with oncology experience for the Montreal/Quebec area (remote). Responsibilities include selection and initiation of investigational sites, monitoring visits (remote and onsite), SDV/SDR/CRF review, drug accountability, CTMS and eTMF maintenance, SAE reporting, regulatory submissions support, and preparation for audits/inspections. Role requires knowledge of ICH-GCP, local regulations, clinical study management and the ability to travel nationally/internationally as required.

Role oversees site identification, qualification, setup, monitoring and closure; manages monitoring activities, regulatory submissions, study essential documents, budgets and study management agreements; develops risk management plans; contributes to patient recruitment strategy; leads and motivates local study teams. Requires minimum 3 years' experience in development operations (CRA/SrCRA or related), fluent Turkish and English, and a bachelor's in life sciences or related discipline.

Role owns and optimizes Microsoft 365 services, drives adoption of M365 Copilot and collaboration tools, ensures platform performance, security, and compliance, partners with business and IT to deliver solutions, establishes standards and documentation, mentors team members, and acts as escalation point for complex issues. Requires deep Microsoft 365 experience, enterprise adoption experience, and strong stakeholder and communication skills; 8–10+ years in large global environments; B.A./B.S. or equivalent experience; Microsoft certifications preferred.

Flexible Turkey-based role (remote with two days/week at sponsor office in Istanbul or Ankara) responsible for end-to-end country start-up from post-feasibility to site activation. Duties include preparing and tracking regulatory submissions, managing contracts and start-up budgets, tracking import licenses and IMP/equipment delivery, ensuring ISF/site readiness, and driving activation timelines. Requires fluency in Turkish and English and knowledge of ICH-GCP and local regulatory requirements.

FSP Clinical Operations role supporting a large pharmaceutical sponsor: lead and manage regulatory submissions and maintenance, maintain Investigator Site File inspection readiness per ICH-GCP and local requirements, oversee site-level contract and budget amendments, and ensure regulatory documentation quality and compliance. Requires experience with local regulatory/MoH procedures and proficiency in Turkish and English.