Responsible for implementing eClinical platforms for studies, gathering and documenting requirements, configuring systems (CTMS, EDMS, EDC, IVRS), coordinating global virtual teams, managing client communications, ensuring compliance with SOPs/ICH-GCP/21 CFR Part 11, and supporting timely, high-quality delivery. Role can be fully home based in Romania, Serbia, Poland, or South Africa.

Parexel is recruiting a Medical Director or Senior Medical Director with a Neurology or Psychiatry background to provide medical monitoring and pharmacovigilance support, contribute to study design and protocol development, review safety (including serious adverse events), support client engagements and potentially lead/mentor medical teams. Requires a medical qualification, qualified psychiatrist or neurologist, and minimum 5+ years clinical practice; excellent English. Locations: remote roles in Croatia, Hungary, Czech Republic, Lithuania, Georgia, Poland, Romania and Serbia.

Parexel seeks a Regulatory Affairs Consultant specializing in global labelling operations to manage end-to-end labelling lifecycle, prepare and review labelling documents for regulatory submissions, maintain labelling databases, and support harmonization initiatives. Role requires labelling/regulatory experience with global responsibilities, CCDS experience, direct Swissmedic experience, a life-science degree, and fluency in German and English.

Parexel is hiring a Global Site Start-Up (SSU) Lead accountable for efficient, compliant site activation and country start-up strategy. Responsibilities include developing site/country start-up strategies, overseeing TMF and regulatory document management, managing CRO/vendor performance, tracking study metrics, and supporting regulatory submissions. Role requires a bachelor’s degree and a minimum of 4 years of global SSU/ regulatory submission and project/clinical trial management experience. Base pay range for Poland is 220,000–250,000 PLN gross annually.

Parexel is hiring a Senior Regulatory Affairs Associate to manage regulatory submissions for clinical trials in South Africa (role can be Bloemfontein-based or remote anywhere in South Africa). The role includes acting as Local Regulatory Contact (LRC), coordinating submissions across participating countries, participating in regulatory operations and project meetings, and supporting local/regional/global projects. Required: science degree, background in clinical trial management, experience with CTAs in South Africa, and fluency in English; experience with Veeva/Clinical Vault, Excel/VBA and Power BI is specified.

Remote role (Poland, Romania, Hungary, Serbia, Lithuania) as Associate Director, Data Engineering (Platform and Analytics). Responsible for lake house strategy (medallion architecture), engineering across ingestion, transformation, storage and optimization, ensuring data quality, security and lifecycle management. Leads and mentors global data engineering teams, champions cloud engineering and tools (notably Azure Databricks), and collaborates with Data & Technology and business stakeholders to enable analytics, AI readiness and sponsor data delivery. Bachelor's in CS/Information Systems (or equivalent experience) required; Master’s preferred. Experience expectations include enterprise cloud data initiatives, medallion architecture implementations, advanced SQL and Python, CI/CD, Power BI (preferred), and familiarity with GxP in life sciences.

Parexel seeks Project Leader and Senior Project Leader candidates to lead global clinical trials (biotech) in dermatology and other therapeutic areas. Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities and supporting the full clinical development process through regulatory submissions. Minimum requirement: undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2+ years leading global clinical trials in project management within CRO/biotech/pharma.

Parexel is hiring a Site Contract Associate to support site contract negotiation, finalisation, execution and amendments for clinical trial site agreements and related documents for the DACH region. The role is remote (Romania or Serbia) and requires fluency in German and English. Responsibilities include ensuring regulatory and legal compliance (including ICH‑GCP), managing execution processes, maintaining records, tracking contracting milestones, and liaising with sites and internal stakeholders. Experience with contract work and MS Office is required; CRO/life‑sciences experience is desirable.

Parexel seeks an MD Endocrinologist (FRCPC or equivalent) to serve as Associate/Medical Director/Senior Medical Director in Endocrinology. Responsibilities include medical monitoring, adverse event review and coding, safety data review, regulatory reporting, protocol and report support, and client/sponsor consultation. Candidates should have clinical experience in obesity, NASH/MASH, and diabetes, strong medical communication skills, and be willing to travel up to 20%.

Parexel is seeking a Principal Consultant with prior FDA experience (ORA/OII/CDER) to advise life sciences clients on FDA regulatory expectations, inspection readiness, remediation, and enforcement response. The role requires deep GMP and inspection experience, including international/foreign cadre inspections and handling of enforcement actions, and involves significant travel (50–70%). Minimum 15 years' related experience and a bachelor’s degree (advanced degree preferred).

Parexel seeks an AI Strategy and Implementation Lead to drive Medical Communications AI strategy and deliver end-to-end implementation of AI-driven solutions (including AI agents on LLM platforms). The role requires demonstrable experience in medical communications or medical affairs, hands-on AI/LLM development and deployment, project and change management, and stakeholder engagement; it is a remote role based in select EMEA countries (listing includes Ireland and the United Kingdom).

Responsible for establishing and leading a high-performing regulatory affairs team in Hong Kong to plan and execute registration strategies, oversee product launch and implementation timelines, and manage external stakeholders (including government and Hospital Authority). Role involves CMC and labelling collaboration, change implementation management, consulting activities, and requires at least 5 years' Hong Kong pharmaceutical experience, proficiency with PRS2.0, and an advanced degree in life sciences. Biologics regulatory experience is preferred.

Parexel is hiring Project Leader (PM) and Senior Project Leader (SPM) roles to provide leadership for mid-to-large global clinical trial projects across therapeutic areas. Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Minimum requirement is 2+ years leading global clinical trials in project management (CRO preferred); advanced degree preferred. Roles are homebased in the United States.

Parexel seeks a Regulatory Affairs Associate to manage regulatory documentation (CPPs, GMP, CMC), coordinate legalisations/translations and vendor relationships, handle registration samples and fee payments, and maintain paper and physical archiving for inspection readiness. Role is full-time, office-based in Marburg and requires a bachelor's degree in a scientific discipline, knowledge of international pharmaceutical regulations and GMP, and strong English skills.

Parexel is recruiting a Clinical Research Associate II (FSP) for cell therapy. Core responsibilities include driving site performance, conducting onsite monitoring and SDV, managing drug accountability and study supplies, ensuring ICH-GCP and local regulatory compliance, preparing monitoring visit reports, supporting data query resolution and SAE reporting, contributing to site selection, and preparing for audits/inspections. Requires minimum 2 years' CRA experience, a bachelor’s degree in a biological or healthcare field, and fluency in English and the host-country language (China).

Parexel is hiring a Clinical Research Associate II to perform onsite site monitoring and related activities in compliance with ICH-GCP and local regulations. Responsibilities include source data verification, drug accountability, SAE reporting, data query resolution, site selection and investigator training. Minimum 2 years' CRA experience and a bachelor's degree in a biological science or healthcare-related field; fluent English and host-country language required.

Parexel seeks a Clinical Research Associate II (FSP) to support cell therapy studies in China (locations include Chengdu/Wuhan). Responsibilities include site monitoring and visit reporting, SDV, site selection, drug accountability, SAE reporting, data query resolution, and audit/inspection preparation. Requires minimum 2 years' CRA experience and fluency in English and the host country language (Chinese).

Parexel seeks a Senior Clinical Research Associate (sponsor-dedicated) based in Belgium to monitor oncology trials. Role requires oncology trial experience and RECIST criteria knowledge. Responsibilities include remote and on-site monitoring per the Study Monitoring Plan, source data verification, CRF review, informed consent verification, pharmacovigilance follow-up, investigational product accountability, query resolution, and ensuring ICH-GCP and local regulatory compliance. Proficiency in the local language and advanced/fluency in English are required.

Parexel FSP seeks a home-based Senior Clinical Research Associate in Israel to manage and monitor oncology study sites for a single client. Requires at least 4 years of oncology and independent site monitoring experience, strong knowledge of clinical trial methodology and GCP/ICH, and skills in site management, mentoring, and stakeholder communication. Role includes remote work with opportunities for travel.

Accountable for full site lifecycle activities (site identification through close-out) including qualification, initiation, on-site and remote monitoring, TMF and regulatory document management, CRF and SAE follow-up, site training, and ensuring compliance with ICH-GCP and study procedures. Requires experience in site management/clinical research, use of CTMS/EDC/EDMS, strong communication and problem-solving skills, and ability to travel extensively.