Jobs at Parexel

Collect clinical data and specimens per protocols and ICH-GCP; perform physiological measurements, phlebotomy, and assist with invasive procedures; operate clinical equipment; maintain CRFs and documentation; participate in quality control, audits, and risk mitigation in an early phase onsite unit.

The role involves designing clinical development programs, conducting statistical analyses, and ensuring evidence aligns with global strategies for Access and HTA needs.

Conduct site monitoring visits, manage site relationships, ensure compliance with protocols, and evaluate trial data integrity in clinical research.

The Senior Clinical Research Associate will ensure compliance with ICH GCP and local regulations, overseeing data integrity and conducting monitoring activities both remotely and on-site, particularly in oncology trials.

The Senior Business Development Director will drive new business acquisition, maintain client relationships, and collaborate on strategic sales plans. Responsibilities include understanding client needs, ensuring effective proposal strategies, and influencing decision-makers to achieve sales goals in a competitive environment.

The Director RWD Strategy leads the implementation of real-world data initiatives in Europe, managing partnerships and proposal development while ensuring compliance with data use agreements.

The Senior Clinical Research Associate is responsible for ensuring data integrity and compliance with protocols in oncology trials, managing monitoring activities and collaborating with site personnel.

The Project Leader/Senior Project Leader will oversee biotech projects, ensuring quality leadership, client satisfaction, and compliance with standards throughout clinical trials in various therapeutic areas.

Support pricing and market access projects by synthesizing clinical, economic, and payer evidence to inform pricing, reimbursement, and HTA strategies. Conduct primary and secondary research, produce high-quality PowerPoint and written deliverables (GVDs, HTA submissions), analyze diverse datasets, and communicate insights to clients while meeting deadlines and maintaining accuracy and compliance.

The Training Development Lead will oversee the design, development, and implementation of global training courses in clinical research and regulation, managing deliverables and stakeholder communication while ensuring compliance with educational standards.

The Senior Clinical Research Associate will manage the operational aspects of clinical trials, ensuring compliance with regulations and monitoring sites to ensure patient safety and quality of studies.

The Executive Director leads HEOR Consulting projects, manages teams, ensures client satisfaction, and drives AI integration within healthcare solutions while overseeing business development and strategic planning.