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Play a crucial role in their 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.
Responsible for developing new and existing businesses within their territory. Meet sales objectives and satisfy customer needs by educating and selling the company product lines and services to research facilities.
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.
Support technical transfer of new processes from concept through product delivery. Design and install new equipment and/or existing equipment modifications to support new process requirements
Identify and pursue new business opportunities in the pharmaceutical and biotechnology sectors related to preclinical discovery and development. Leverage a strong technical background in preclinical research, with a focus on immuno-oncology, oncology, degenerative disorders, or related areas to effectively communicate with clients and internal teams.
Ensure all reviewed and awarded biomedical research grants are in compliance with internal policy, ethical, financial, legal requirements, and are in line with the foundation's overall vision. Conduct post award monitoring of projects, review all requested changes to the award, and approve changes that are consistent with Foundation policies and procedures.
Guarantee the alignment of research grants with internal policy, ethics, finance, and legal standards while nurturing my client's overarching vision. Meticulously oversee awarded projects, granting your valuable input into award modifications, in harmony with the foundation's policies and procedures.
Create and pioneer innovative synthetic pathways for pharmaceutical APIs within our cutting-edge laboratory, then seamlessly scale up these processes to kilogram-level production within our internal facilities. Uphold meticulous record-keeping practices in compliance with company policies, ensuring the traceability and transparency of experiments.
As a vital member of the team, the Process Engineer leads the design, installation, and implementation of processes and equipment to ensure the safe, compliant, and efficient production of small molecule active pharmaceutical ingredients (APIs) in a GMP environment.
Develop and manage portfolio of grants and partnerships in aging biology and longevity research, with a focus on Physiology grants. Help assist the Senior Directors in the formulations and implementation of funding and development strategy.
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.
Provides scientific expertise in the development of methods and method validations. Maintain laboratory equipment, including troubleshooting and repair of LC-MS/MS and GC-MS/MS instruments.
Identify, cultivate, and maintain relationships with new and current clients. Achieve quarterly and annual sales goals.
Lead clinical development team and manage Phase I - Phase III trials. Join dynamic fast-paced company while working directly with senior leadership
Design and develop novel synthetic routes to pharmaceutical APIs in the laboratory and implementing the processes at kilogram-scale in internal facilities. Maintain clear and accurate records of experiments in laboratory notebooks in accordance with company policy.
The Scientific Review Supervisor oversees the thorough screening of grant applications to ensure completion and accuracy, and orchestrates peer-review meetings to assess their merit. They deliver comprehensive reports to Program Officers, summarizing reviewer scores and providing concise evaluations to applicants and staff.
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.
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 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 Senior Formulation Scientist position is responsible for business continuity activities that include qualifying new/alternate raw materials (fragrances, surfactants, dyes, preservatives etc.), new applicators and packaging components, developing new processing methods to aid scale up and Production, troubleshooting commercial batches and help in process development and cost-saving initiatives to support all products made.
As a Field Clinical Account Specialist you will be providing educational, clinical, and procedural direction to help achieve patient care, customer support, and service objectives. You will interface with and help our customers by being the resident expert on our Hepatic Arterial Infusion (HAI) pump and accessories
My client is seeking a highly skilled and motivated Field Service Engineer to provide technical support, installation, repair and maintenance of our analytical instruments at customer sites. The Field Service Engineer will be responsible for ensuring that our customers receive exceptional service and support, in order to maximize their satisfaction and the performance of our products.
The Operations Manager will be hands on in the development of new projects and overseeing and growing a team of engineers and technicians.
The Principal Systems Engineer will lead cross-functional efforts to implement aesthetic laser system projects, defining requirements and overseeing the development of system specifications. They will also conduct testing, document results, and generate final reports with a focus on subsystem interfaces and design verification.
The Electrical Systems Engineer will lead development efforts of the product system accessories. This is a hands-on position that will provide the opportunity for the right individual to build and manage a team.
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