Lead Hepatology Clinical Development Scientist

GSK; Greater London; On-site; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Annual bonus

Healthcare

Pension plan membership

Shares and savings programme

Job summary

GSK is seeking a Clinical Scientist, Hepatology Clinical Development, to lead design, execution, analysis, and reporting of hepatic studies across development phases. Collaborate with medical monitoring, biostatistics, data management, and regulatory teams.

On-site role based in London or Waltham with no hybrid option. The role emphasizes scientific and operational expertise to generate high-quality clinical data, with opportunities to contribute to Investigator’s Brochures and regulatory

Qualifications

• Required PharmD/PhD/MD or equivalent.
• Minimum of 3 years of clinical research or drug development experience.
• Preferred: experience drafting study protocols and safety oversight; strong cross-functional collaboration; solid understanding of GCP and global regulations.

Responsibilities

• Contribute to clinical development plans and study design.
• Support protocol, amendment and informed consent development.
• Evaluate emerging scientific and competitive data.
• Participate in feasibility and site selection activities.
• Partner with Clinical Operations to oversee study conduct.
• Monitor enrollment, protocol deviations and study performance.
• Prepare and review CSRs, abstracts and presentations.
• Support advisory boards and regulatory submissions.

Skills

Clinical development

Clinical trial designs

Decision making

Leadership

Teamwork

Project management

Risk management

Strategic thinking

Education

PharmD, PhD, MD or equivalent

Job description

GSK is seeking a Clinical Scientist, Hepatology Clinical Development, to lead design, execution, analysis, and reporting of hepatic studies across development phases. Collaborate with medical monitoring, biostatistics, data management, and regulatory teams.

On-site role based in London or Waltham with no hybrid option. The role emphasizes scientific and operational expertise to generate high-quality clinical data, with opportunities to contribute to Investigator’s Brochures and regulatory