Bioanalysis and Toxicokinetics Project Manager - Client-dedicated

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description 6-month fixed term opportunity Location: Hybrid, Cambridge Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner.  Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Join Us as a Bioanalysis and Toxicokinetics Project Manager – Make an Impact at the Forefront of Innovation!

We are looking for an experienced Scientific Project Manager to provide flexible scientific and project-management support across Bioanalysis (BioA), Toxicokinetics (TK) and cross-functional operational improvement activities. The role will provide experienced, responsive review of BioA and TK reports on an ad hoc basis, while also helping to establish and project manage a portfolio of drug discovery and development activities using Airtable as a new operational platform. The successful candidate will also contribute to ongoing improvement initiatives focused on strengthening ways of working across Toxicology and Bioanalysis teams. This is a varied position combining scientific report review, project management, digital workflow implementation and process improvement.

Airtable Platform Setup & Project Management Work with key stakeholders to configure Airtable workspaces, bases, views and workflows for selected drug discovery and development projects. Translate project needs into practical tracking tools for milestones, deliverables, ownership, status, risks, dependencies and decision points. Maintain project trackers and dashboards to support visibility of non-clinical delivery activities across multiple programmes. Coordinate project-management routines, including action tracking, follow-up, status reporting and escalation of risks or delays. Support adoption of Airtable by developing simple instructions, templates and ways-of-working guidance for end users. Bioanalysis & Toxicokinetic Report Review Review bioanalytical and toxicokinetic reports on an ad hoc basis, ensuring scientific accuracy, internal consistency and appropriate interpretation of study data. Check that report content is aligned with agreed study objectives, sample-analysis plans, method-validation expectations and relevant regulatory/scientific guidance. Identify data inconsistencies, calculation issues, reporting gaps or unclear conclusions, and provide concise, actionable comments to study teams or CRO partners. Support timely resolution of report-review comments to enable efficient study close-out, decision-making and regulatory readiness. Process & Ways-of-Working Improvement Contribute to ongoing process-improvement activities across Toxicology and Bioanalysis teams. Support development of pragmatic process improvements, including clearer roles, timelines, escalation routes and documentation expectations. Capture agreed actions, track progress and prepare concise updates for relevant working groups or leadership discussions. Promote consistent, transparent and efficient ways of working across cross-functional teams.

We are looking for candidates who can demonstrate: Experience in bioanalysis, toxicokinetics, DMPK, non-clinical development, clinical pharmacology operations or a closely related scientific/project-management environment. Ability to critically review scientific reports and identify issues in data interpretation, consistency, terminology and conclusions. Strong project-management capability, with confidence managing multiple