Parexel is hiring project management professionals for its Biotech Division to lead global clinical trials in Neurology, Psychiatry and Rare Disease. Roles include Project Leader, Senior Project Leader and Project Director; candidates should have a minimum of 2+ years leading global clinical trials (CRO/biotech/pharma preferred) and experience in scheduling, resource and budget management, team coordination and regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader (and higher) candidates to lead global clinical trials for biotech clients across multiple therapeutic areas (including Neurology, Oncology/Hematology, Respiratory, Cardio, General Medicine and GLP-1/Obesity). Requires at least 2+ years leading global clinical trials in a CRO, Biotech or Pharma, experience with scheduling, resource and budget management, team coordination, and the full clinical development process through regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader candidates to lead Metabolic / GLP-1 / Obesity global clinical studies. Roles involve leading project teams, managing day-to-day operations, project scheduling, resources and budgets, 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' experience leading global clinical trials in a CRO, biotech, or pharma setting.

Parexel FSP seeks a Clinical Trial Coordinator to support study start-up through closure, including trial/site administration, document and eTMF management, regulatory/IRB support, and budgeting/contract/payment activities (including budget negotiation and FCPA documentation). Position is hybrid with a minimum 1-day onsite requirement in Kirkland, Quebec. Minimum 1–2 years clinical research or relevant healthcare experience; business‑proficient English required.

Parexel is hiring a home-based Clinical Research Associate in Poland dedicated to a single sponsor, responsible for site management and supervisory activities for oncology studies. Requires science education, minimum 1 year of independent site monitoring experience, knowledge of clinical trial methodology, and working knowledge of GCP/ICH and local clinical research legislation.

Parexel seeks a CRA II/Senior (FSP) based in NSW or VIC, Australia (remote/North Ryde location noted). Responsible for site monitoring and oversight per the Study Monitoring Plan from site activation through database lock, AE/SAE management, TMF and documentation, recruitment support, and study close-out. Requires minimum 3 years CRA/site monitoring experience (preferably oncology experience), bachelor’s degree in life sciences or equivalent, fluency in English, significant regional travel (60–80%), and valid driver’s license and passport.

Parexel is hiring a Site Contract Leader to act as primary sponsor interface and lead end‑to‑end site contracting strategy and execution for global clinical trials. The role includes negotiating contracts, developing and assessing investigator budgets (not template‑driven), guiding project site contracts teams, managing timelines and budgets, and ensuring alignment to protocol and study objectives. Requires 3+ years in site contracting or a closely related CRO role and advanced MS Excel skills.

Parexel is hiring a remote Site Contract Associate based in Argentina, Mexico, or Brazil. The role is responsible for negotiating, finalizing and executing site contracts and amendments, managing budgets and ensuring documents meet regulatory requirements (including ICH‑GCP). Requires 2+ years' relevant experience, fluent English, strong Excel and negotiation skills, and a university degree (law or similar preferred).

Senior Biostatistician responsible for designing and executing complex statistical analyses for clinical trials and observational studies, contributing to protocols and statistical analysis plans, authoring reports and manuscripts, performing quality control of statistical deliverables, coordinating with clients and cross-functional teams, and coaching junior biostatisticians. Requires graduate degree in statistics/biostatistics and industry experience.

Fully remote role for candidates based in South Africa. Lead complex clinical data engineering projects: implement data receipt agreements, design data ingestion procedures using SAS/Workbench/SQL/R, create reconciliation checks and offline listings, aggregate data from multiple sources, maintain documentation and regulatory compliance (ICH-GCP, 21 CFR Part 11, SOPs), mentor teams, and act as a client-facing subject matter expert.

Parexel seeks a Senior Clinical Data Engineer based in South Africa (fully remote) to support global clinical trials. The role includes programming and configuring data ingestion (SAS, Workbench, R, SQL), performing reconciliation checks and custom reports, aggregating and managing external data, ensuring compliance with SOPs and regulations (ICH-GCP, 21 CFR Part 11), maintaining study documentation, leading programming teams, and driving process improvements. Applicants must reside in South Africa and be legally authorized to work there.

Parexel seeks an experienced Study Physician to be medically responsible at the trial level through preparation, conduct and reporting of clinical trials for a dedicated sponsor in EMEA. Responsibilities include medical oversight from trial design to Clinical Trial Report, protocol preparation, risk-based quality management, co-authoring clinical quality monitoring plans, and ongoing medical data review. Requires an MD with a minimum of 4 years active clinical practice; specializations such as pulmonology, immunology, internal medicine, infectious diseases, family medicine, pediatrics, rheumatology or emergency medicine are desirable. Experience in pharma/CRO, clinical development or pharmacovigilance and familiarity with ICH-GCP and data/IT systems are advantageous.

Lead and execute GxP audits (including GMP/GLP/GCLP, TMF, safety/PV and supplier audits), manage audit programs and client relationships, provide QA consultancy, support regulatory inspections and mentor auditors. Role requires experience in quality assurance/auditing and clinical research regulations.

Parexel seeks a Senior/Regulatory Affairs Consultant (Regulatory Labeling Strategist) to lead global labeling strategy and governance (CDS, USPI, SmPC, patient leaflets), manage labeling operations and documentation (eDMS, RIMS), engage with health authorities (FDA, EMA), oversee advertising/artwork review, and support global implementation. Role requires ~5+ years pharma/biotech experience with at least 2 years in global labeling.

Deliver medical support and medical monitoring activities for clinical studies (including medical review of data, safety/serious adverse event review, medical input to PV workflows and regulatory safety reporting). Participate in study planning, protocol and study document development, training of study teams, audits/inspections, rotas for emergency medical contact, client engagement and support business development/proposal activities. Requires medical qualification, clinical practice experience, knowledge of GCP/ICH/FDA/EMEA guidelines and a minimum of 3 years' medical monitoring or medical data review experience.

Manage early-phase clinical studies from pre-award/bid defense and start-up through implementation and close-out. Own sponsor communications, lead kick-offs, oversee site selection, IRB/EC and RA processes, monitor timelines, recruitment and data cleaning, track budgets via CTMS, prepare for audits, identify and mitigate risks, and provide oversight and training to junior project staff. Requires a science-related bachelor's (advanced degree preferred) and 2 years' PM experience with Parexel or 3–5 years in related fields; knowledge of ICH-GCP and proficiency in MS Office.

Responsible for post-approval regulatory lifecycle tasks including preparation and submission of variations, renewals, MA transfers, and Module 1 activities. The role manages local health-authority submissions (including RIMS/Veeva Vault), supports linguistic and artwork reviews, assists with DHCP and PSUR activities, and contributes to country-level regulatory intelligence.

Parexel seeks an experienced Study Physician/Medical Director to be medically responsible at the trial level for a sponsor in the EMEA region. Responsibilities include medical oversight from trial design through reporting, protocol preparation, defining medical risk-related data for quality plans, co-authoring clinical quality monitoring plans, and ongoing medical data review. Requires MD with minimum 4 years active clinical practice; clinical specialties (e.g., pulmonology, immunology, internal medicine, infectious diseases, pediatrics, rheumatology, emergency medicine) and experience in clinical development, CRO/pharma, pharmacovigilance, and ICH-GCP are desirable.

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 recruiting a Senior Clinical Research Associate (Oncology) for the Montreal/Quebec area (remote). The role includes site selection, initiation, monitoring and closure in compliance with ICH-GCP and local regulations; responsibility for CTMS/eTMF updates, SDV/SDR, drug accountability, SAE reporting, and support for audits and inspections. Travel nationally/internationally is required as needed.