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Drive pioneering clinical development initiatives in the small molecule space, advancing novel therapeutics and shaping the future of healthcare. Lead groundbreaking research and contribute to transformative treatments in the dynamic biotech landscape.
Lead clinical development team and manage Phase I - Phase III trials. Join dynamic fast-paced company while working directly with senior leadership
This is a prestigious opportunity for a VP/SVP of Partnerships to play a pivotal role in a leading Life Science company. The successful candidate will spearhead collaborations, develop strategic partnerships, and champion growth initiatives across the US with flexible working out of the HQ in San Francisco.
Reporting into the General manager, The Director of Quality & Regulatory will direct the organisation's Regulatory Affairs and Quality Assurance functions in multiple areas including documentation, compliance, audits and regulatory submissions.
My client is seeking a Director of Quality located near Chicago, IL. The Director of Quality Control will develop, implement, and periodically evaluate a program to ensure the organization's production operations, from raw materials to finished products, meet the quality, integrity, and efficiency standards set by the organization.
Identify, cultivate, and maintain relationships with new and current clients. Spearhead the development of business at a quickly growing, impactful CDMO in the pharmaceutical industry.
Play a crucial role in our clinical development team, providing strategic medical leadership in the development of novel drugs and therapies. Responsible for US Clinical development and will offer medical guidance to discovery projects, ensuring the highest standards of clinical research.
Identify, cultivate, and maintain relationships with new and current clients. Achieve quarterly and annual sales goals.
Play a crucial role on the clinical development team, providing strategic medical leadership in the development of novel drugs and therapies. Responsible for US Clinical development and will offer medical guidance to discovery projects, ensuring the highest standards of clinical research.
The Divisional Chief Financial Officer role plays a pivotal role in optimizing financial performance, advancing strategic planning, and fostering the growth of 2/3 of their overall business.
Uncover and secure new business opportunities in your designated territory. Thrive as an independent contributor in the dynamic large molecule bioanalytical domain, specializing in early-phase clinical services.
Take the helm as the main liaison for vital pharmaceutical clients, managing every facet of alliance management. Cultivate lasting relationships, working collaboratively to ensure shared success.
Elevate the company's prominence by fostering beneficial collaborations, advocating our integrated services to potential partners. This role bridges science and business, building enduring relationships while aligning drug discovery and CMC capabilities.
As a Engineering Manager, you will lead the design, development, and commercialization of our novel combination devices. In this role, you will be responsible for managing and executing all aspects of device development, from concept generation and prototyping to validation and manufacturing transfer.
Lead and oversee the dynamic process of managing biomedical grant awards, ensuring seamless coordination between key departments including Operations, Science Team/Program Directors, Legal, and Finance. Drive continuous improvement by updating and refining the Grants Management policy handbook, contributing to the advancement of groundbreaking biomedical research initiatives in the emerging field of Aging Biology and Healthspan Sciences.
Take the lead in establishing and optimizing Antibody Drug Conjugate (ADC) manufacturing processes from inception to full-scale operation. Lead a dedicated team to drive efficient downstream operations in ADC production, ensuring successful project delivery.
Manage $50 million DMPK service business and lead a team of 3 direct reports at the Senior/Director level. Act as a "player coach" to bring in new high level clients and grow/develop the team.
Lead regulatory affairs in our small molecule pharmaceutical company, spearheading FDA interactions and medical writing to ensure compliance and successful product development. Your expertise will drive regulatory strategies, ensuring the approval and commercial success of small molecule therapies.
Lead the curation of grants and partnerships for cutting-edge research in aging biology and longevity with a focus as it pertains to physiology. Collaborating with Senior Directors to shape innovative funding and development strategies.
Provide regulatory expertise through all stages of the product lifecycle, including development of CMC strategy. Perform regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for the site, oversees the TSE/BSE program, and provides compliance documents to support Health Authority submissions
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