Parexel International Romania SRL is the Romanian entity of Parexel, a global clinical research organization that provides clinical development services for pharmaceutical, biotechnology, and medical device companies. Its core work includes clinical trials, regulatory consulting, medical communications, and market access support, positioning it as a large enterprise CRO within the healthcare and pharma services sector.

Products & services

Integrated Clinical Development Whole-study clinical development services spanning Phase IIb-IV trials, protocol design, site management, data operations, patient inclusion, technology, logistics, and safety oversight.
Early Phase Clinical Trials Phase I and selected Phase Ib/IIa clinical trial services, from first-in-human studies through early patient studies, supported by dedicated clinical units and clinical pharmacology expertise.
Regulatory Strategy, Submissions, Compliance, and Outsourcing Global regulatory consulting and operational support covering regulatory strategy, dossier preparation, health-authority submissions, compliance, audits, and post-approval regulatory activities.
Real-World Evidence Real-world research and evidence-generation services that use routine-care data and post-approval studies to support clinical, regulatory, payer, and commercial decisions.
Market Access Strategy and Delivery Market access consulting that aligns clinical, regulatory, health-economic, and evidence plans with payer, HTA, pricing, reimbursement, and launch requirements.
Drug Safety and Pharmacovigilance Clinical and post-marketing pharmacovigilance services for collecting, assessing, processing, and reporting safety information throughout a product’s lifecycle.

Seniority mix

Entry & junior 0 roles
Mid-level 1 role
Senior 7 roles
Lead & principal 0 roles
Manager & above 1 role

Based on 9 open roles

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