
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
Selected: 🆕 Date Added.
🕒 Yesterday
Senior Regulatory Strategist guiding FDA advertising and promotion compliance at Parexel, a global clinical development partner. Advising cross-functional teams and shaping regulatory strategy for clinical and commercial activities.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🚔 Compliance
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Senior Regulatory Affairs Associate managing US-based CTA submissions and regulatory compliance for Parexel, a global clinical development partner. Coordinating health-authority interactions, CROs, and cross-functional submission teams.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🚔 Compliance
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Regulatory strategy consultant leading submissions and development pathways for Parexel’s biopharmaceutical clinical research programs. Guiding regulatory decisions, lifecycle planning, and cross-functional collaboration.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🔴 Lead
🧐 Strategy
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Regulatory strategy associate guiding pathways, submissions, and FDA compliance for vaccine and biologic development at Parexel. Remote role supporting clinical research and new therapies.
🕒 Yesterday
Global Regulatory Labeling Strategist shaping compliant labeling for Parexel’s clinical development and regulatory solutions. Leading TPL, CCDS, regional strategies, and health authority submissions across global markets.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🚔 Compliance
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 Yesterday
Manager leading 24x7 applications support and technical service delivery at Parexel, a global clinical development partner. Resolving complex issues, managing support teams, and improving customer satisfaction.
🕒 Yesterday
Senior Physician guiding pharmacovigilance and patient safety at Parexel, a global clinical development partner. Reviewing safety cases, signals, aggregate reports, and regulatory submissions.
🕒 2 days ago
Senior Clinical Research Associate supporting Parexel’s oncology clinical trials in Belgium. Ensuring site compliance, patient safety, data integrity, and inspection readiness through remote and on-site monitoring.
🇧🇪 Belgium – Remote
💰 Venture Round on 1990-01
⏱ Part Time
🟠 Senior
🧪 Clinical Research
👻 Ghost score 10%
🕒 2 days ago
Supply and Logistics Specialist managing clinical supply, sourcing, inventory, and logistics projects at Parexel. Supporting clinical trial development and regulatory services that improve global health.
🇨🇳 China – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Logistics Specialist
👻 Ghost score 10%
🕒 2 days ago
Associate Medical Safety Director leading oncology drug safety and signal management at Parexel. Driving patient safety, regulatory compliance, and pharmacovigilance improvements.
🕒 2 days ago
Senior Statistical Programmer creating SAS datasets, tables, listings, and figures for Parexel’s clinical trials. Supporting validation, regulatory submissions, and programming standards for sponsor projects.
🌐 Poland, Hungary, +2 more countries – Remote
💵 zł200k - zł260k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🖥 Software Engineer
👻 Ghost score 0%
🕒 3 days ago
Senior Manager optimizing Salesforce, enablement, and commercial campaigns for Parexel’s global clinical research business. Driving Inside Sales effectiveness across biotech and pharmaceutical clients.
🇺🇸 United States – Remote
💵 $115k - $120k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
📊 Sales Operations
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 3 days ago
Clinical Research Associate monitoring clinical trial sites for Parexel, a global clinical research organization. Ensuring patient safety, data quality, regulatory compliance, and site delivery.
🕒 3 days ago
Senior Patient Recruitment Lead advancing patient recruitment for Parexel, a global clinical research organization. Leading engagement strategies, client communications, KPIs, vendors, and study-team collaboration.
🕒 3 days ago
Regulatory publishing consultant supporting eCTD systems and regulatory technology for Parexel’s global clinical research services. Troubleshooting, validating, and advising clients on submission platforms.
🇨🇦 Canada – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance
👻 Ghost score 10%
🕒 3 days ago
Senior PK Analyst programming and validating pharmacokinetic datasets and analyses for Parexel’s clinical development solutions. Mentoring analysts and leading quality and process improvements.
🕒 4 days ago
Regulatory publishing consultant supporting eCTD and regulatory systems for Parexel’s global clinical research solutions. Troubleshooting platforms, validating technology, and advising clients on regulatory submissions.
🇨🇦 Canada – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance
👻 Ghost score 10%
🕒 4 days ago
CMC Regulatory Affairs Associate authoring M3 biological-product submissions for Parexel’s global clinical development services. Managing CMC packages, eCTD sequences, Health Authority queries, and multi-region regulatory coordination.
🌐 Mexico, Argentina, +1 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🚔 Compliance
👻 Ghost score 10%
🕒 4 days ago
Senior Clinical Research Associate monitoring clinical trials for Parexel’s clinical development solutions. Ensuring GCP compliance, site performance, and patient recruitment across California-based studies.
🏄 California – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 4 days ago
Senior Clinical Research Associate managing investigator sites and monitoring clinical trials for Parexel’s clinical development services. Ensuring patient safety, GCP compliance, recruitment, and study quality.
🏈 Ohio – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 10%
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