Biotechnology Jobs in Reading

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• Reading
• Mid-level

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, with a focus on oncology studies. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team partnering with smaller emerging biopharma companies.

Trial Master File · Investigator's Site File

• Reading
• Senior

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.

• Reading
• Remote
• Senior
• Permanent

Supports Pharmacometrics by programming, validating and delivering NONMEM-ready PK/PD datasets from SDTM/ADaM sources using advanced R, covering pre-lock and post-lock clinical data. Includes QC of datasets from external partners and of custom R packages, plus liaison with Data Management, Biostatistics and Bioanalytical teams and regulatory submission deliverables.

R · NONMEM · SDTM +1

• Reading
• Mid-level

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a sponsor-dedicated team, liaising with sites and study team members.

• Reading
• Remote
• Director
• Permanent

Provides strategic medical and scientific subject matter expertise in obesity, cardiology, endocrinology or nephrology, leading proposal development and bid defence meetings as a medical director. Acts as a consultant across the research and development lifecycle and clinical trials, formulating clinical development plans and leading the strategic direction of a Center of Excellence. Requires a terminal MD degree and board certification, with occasional national or international travel.