Biotechnology Jobs

• Zug, Switzerland
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Leads global development of an oncology medicine from clinical proof of concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site.

• London
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Strategically leads global development of an oncology medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and leads a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance, budgets and lifecycle planning.

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Reading
• Remote
• Lead

Lead end-to-end clinical data management for complex global trials, from study setup through database lock, acting as the primary client contact for data deliverables. Oversee SAE, PK and external data reconciliation, manage timelines and budgets, mentor junior staff, and drive process improvements using Medidata Rave or Oracle InForm.

Medidata Rave · Oracle InForm · EDC +1

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.

CTMS · eTMF

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• Maidenhead
• Hybrid
• Senior

Leads clinical data management for one or more oncology studies within a sponsor-dedicated (FSP) model, acting as the primary client contact from study set-up through close-out. Combines strategic oversight of vendors, budgets and CDM deliverables with hands-on work such as eCRF design and data cleaning, collaborating with data coordinators and statistical programmers.

eCRF

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC

• New York, United States
• Hybrid
• US$321,800 – US$443,080 pa
• Director · manages people

Sets enterprise strategy for clinical pharmacology, pharmacometrics and model-informed drug development across a clinical portfolio, owning dose strategy from first-in-human through registrational development. Leads quantitative approaches including population PK, PK/PD, PBPK and QSP, represents the company in health authority interactions, and builds a high-performing function within an AI-native TechBio.

Recursion OS

• Remote Opportunity - United States
• Remote
• US$261,800 – US$346,060 pa
• Director

Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.

WinNonlin · Monolix · NONMEM +1

• Uxbridge
• Director

Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.

• Uxbridge
• Director

Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, focused on Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build AI-driven tools and automate clinical reporting, while collaborating with programming experts across disease areas.

SAS · R · Python +4

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2