Biotechnology Jobs

497 jobs for “Clinical Data Manager/ Snr Clinical Data”

Results

GSK logo

GSK · 10000+ people · Public

Senior, AI Product Manager (Process Development Science)

Save job
  • Stevenage
  • Hybrid · 2–3 days in office
  • Senior

Sits within GSK's Chemical Manufacturing & Control function, identifying and sizing AI opportunities across process development science for oligonucleotides, ADCs and monoclonal antibodies. Partners with forward deployed engineering pods to turn ambiguous business problems into scoped, buildable products, and shapes self-driving lab and in silico modelling initiatives.

Self-Driving Labs · Agentic Workflows · Physical AI

Last week
GSK logo

GSK · 10000+ people · Public

Senior, AI Product Manager (Process Development Science)

Save job
  • London
  • Hybrid · 2–3 days in office
  • Senior

Sits within GSK's CMC function, identifying and sizing AI opportunities across process development science for oligonucleotides, ADCs and monoclonal antibodies. Partners with forward deployed engineering pods to turn ambiguous business problems into scoped, buildable products, and shapes self-driving lab and in silico modelling initiatives.

AI Platforms · ML Platforms

Last week

Autolus · 101–500 people · Series C

Cell Therapy Account Executive (South UK)

Save job
  • United Kingdom
  • Remote

Field-based commercial role owning relationships with Advanced Therapy Treatment Centres across the South UK, acting as the primary point of contact for CAR T therapy accounts. Responsibilities span site onboarding and qualification, coordinating patient treatment logistics and chain of identity, compliance audits, and strategic account planning with Marketing, Medical Affairs and Market Access. Requires deep haematology/oncology and cell therapy expertise, with around 80% travel.

Last month

Autolus · 101–500 people · Series C

Cell Therapy Account Executive (South UK)

Save job
  • London
  • Remote

Primary point of contact for Advanced Therapy Treatment Centres in the South UK, driving appropriate utilisation of CAR T therapies and coordinating site qualification, setup and patient treatment logistics. Works cross-functionally with Marketing, Medical Affairs and Market Access, and is 80% field based with UK travel.

Last month

IQVIA

Clinical Monitoring Analyst (Cluepoints)

Save job
  • London
  • Remote
  • Lead

Supports the Centralized Monitoring Lead in building study-specific monitoring strategies, programming quality tolerance limits, key risk indicators and data visualisations on the Cluepoints platform. Handles platform setup, scheduled refreshes, specification documents and peer reviews, working directly with a sponsor on a dedicated project. Requires strong SAS macro skills and prior data management experience.

Cluepoints · SAS · EDC Systems +1

Today
Novartis logo

Novartis

Lead Central Monitor

Save job
  • Dublin, Ireland
  • Hybrid
  • €63,600 – €118,000 pa
  • Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence

Last month
Novartis logo

Novartis

Lead Central Monitor

Save job
  • Barcelona, Spain
  • Hybrid
  • €63,600 – €118,000 pa
  • Lead · manages people

Lead and develop a team of Central Monitors, shaping central and site monitoring strategies across a global development portfolio. Oversee trial-data surveillance, risk reviews and signal detection using Central Monitoring technology, translating complex risk signals into actionable insights for Clinical Trial Teams. Partners with clinical, data and risk-surveillance teams to strengthen risk-based monitoring and Risk-Based Quality Management.

Artificial Intelligence

Last month

Bristol Myers Squibb

Senior SDTM Statistical Programmer

Save job
  • Uxbridge
  • Hybrid
  • Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

2 weeks ago

AstraZeneca · 10000+ people · Public

Senior Director, Competitive Intelligence, Oncology R&D

Save job
  • Gaithersburg, United States
  • On-site
  • US$218,330 – US$327,494 pa
  • Director

Leads competitive intelligence for AstraZeneca's oncology R&D, owning delivery of clinical and commercial analysis that shapes therapy-area strategy and portfolio investment decisions. Works with a specialist team and senior leadership, translating complex data into insights and challenge. Requires oncology, clinical or investment analysis background.

Last month

AstraZeneca · 10000+ people · Public

Senior Director, Competitive Intelligence, Oncology R&D

Save job
  • Cambridge, United States
  • On-site
  • US$218,330 – US$327,494 pa
  • Director

Leads competitive intelligence for AstraZeneca's oncology pipeline, delivering clinical and commercial analysis that shapes therapy-area strategy and investment decisions. Partners with senior leadership and cross-functional teams, providing respectful challenge and insight into the evolving oncology landscape. Requires oncology, clinical research or investment analysis background with strong communication and influence skills.

Last month
Isomorphic Labs logo

Isomorphic Labs · 201–500 people · Series A

Senior Research Investigator / Research Leader (Translational Pharmacology)

Save job
  • London
  • Hybrid · 3 days in office
  • Senior

Lead translational pharmacology for an AI-first drug discovery team, shaping neurodegeneration strategy and target validation. Bridge dry-lab predictive models with experimental biology, designing screening cascades and profiling AI-designed molecules. Manage CRO partnerships and serve as scientific lead for portfolio programs.

SPR · TR-FRET · Mass Spectrometry

Last week

Gilead Sciences

Sr Director, Medical Writing

Save job
  • Cambridge
  • Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday

Last month

Fortrea

Medical Writer I Yorkshire

Save job
  • Leeds
  • Hybrid · 3 days in office
  • Entry level
  • Permanent

Develops protocols and clinical study reports for early-phase trials (I-IIa), focusing on safety and pharmacokinetics. Coordinates cross-functional teams and client stakeholders to drive documents from draft to final deliverable, with on-the-job training in medical writing.

5 days ago

Parexel

Senior Statistical Programmer (SAS Programmer) - FSP: UK, Hungary, Poland or Serbia

Save job
  • Lisburn
  • Senior · manages people

Senior Statistical Programmer supporting clinical trials within Parexel's FSP team, producing and QCing SDTM and ADaM datasets, tables, figures and listings using SAS. The role can act as Statistical Programming Lead, coordinating global teams, timelines and budgets while liaising with sponsors and Biostatistics and Data Management leads. It also involves mentoring staff and ensuring compliance with ICH-GCP and CDISC standards.

SAS

Last month

Parexel

R0000045029 Senior Statistical Programmer (R Programming) - UK, Poland, Serbia, Hungary - FSP

Save job
  • Harrow
  • Remote
  • Senior · manages people

Senior Statistical Programmer role focused on R programming for clinical trial analysis and reporting, producing and QCing SDTM/ADaM datasets, tables, figures and listings. The position can act as Statistical Programming Lead, coordinating global teams, managing timelines and budgets, and liaising with sponsors and biostatistics. Dedicated to a single sponsor within an FSP model across UK, Poland, Serbia and Hungary.

R · SDTM · ADaM +1

3 months ago

Get new Clinical Data Manager/ Snr Clinical Data... roles by email. One email a morning when new roles match. Stop any time.

Are you sure?