490 jobs for “Clinical Data Manager - Early Phase”
Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May mentor other physicians on complex multi-study programs.
AI
Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, regulators and cross-functional matrix teams. May guide other physicians on complex multi-study programs.
AI
IQVIA
Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, maintains inspection-ready documentation and mentors junior team members, with up to 40-60% regional travel.
Investigator Site Files · Trial Master Files
IQVIA
Monitors clinical trial sites across the UK, performing selection, initiation, monitoring and close-out visits in line with GCP and sponsor requirements. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint +2
Parexel
A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.
SAS · R · MATLAB +1
Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.
DSUR · PSUR · RMP +2
Provides medical and scientific expertise on clinical safety across a product's lifecycle, with emphasis on signal detection, risk management and regulatory submissions. Chairs the Safety Management Team, oversees aggregate reports such as DSURs, PSURs and RMPs, and acts as the safety representative in cross-functional development and post-marketing teams.
DSUR · PSUR · RMP +3
Talentmark
Process, analyse and interpret omics data from clinical portfolio studies to uncover biological mechanisms, treatment effects and safety signals. Develop analysis pipelines using state-of-the-art tools, document reproducible code for patient-level data, and write reports and scientific publications. Requires strong bulk and single-cell RNAseq expertise, R, HPC/Unix and Docker skills.
Docker · DNAnexus
Bristol Myers Squibb
Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.
Moderna · 1001–5000 people · Late stage
Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.
Thermo Watson LIMS · Watson LIMS · LabVantage eLBN +1
Johnson & Johnson Innovative Medicine
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
Fortrea
On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.
eSource · EDC
Autolus · 101–500 people · Series C
Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.
SaaS · APIs · Cloud Data Platforms
McGregor Boyall
Client-facing consulting role in a global technology consultancy's Data & AI practice, serving pharmaceutical and Life Sciences clients. Combines hands-on Data Science, ML and GenAI delivery with strategy, pre-sales and senior stakeholder engagement, focused on commercial applications such as sales, marketing and customer analytics.
Python · SQL
Fortrea
Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.
MHRA · cGMP · NHS Trust
