Clinical Scientist, Hepatology Clinical Development

GSK • Waltham, MA

3d • Onsite

About The Position

The Clinical Scientist is a key member of the Clinical Development team, contributing scientific and operational expertise to the design, execution, analysis, and reporting of clinical studies across all phases of development. The role works closely with Clinical Development, Medical Monitoring, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and external investigators to support successful study execution and high-quality clinical data generation.

The position is based on-site in either Waltham, Massachusetts, or GSK Headquarters in London, United Kingdom. Hybrid and remote work options are not available. The role supports clinical development planning, study conduct and oversight, data review and interpretation, and preparation of scientific and regulatory materials.

Requirements

• Minimum of a PharmD, PhD, MD, or equivalent.
• At least 3 years of clinical research or drug development experience.

Nice To Haves

• Experience drafting or reviewing clinical study protocols, informed consent forms, and clinical study reports.
• Experience providing medical monitoring or clinical safety oversight.
• Ability to work effectively in cross-functional teams and with external partners.
• Strong understanding of GCP and global regulations.
• Excellent communication and collaboration skills.

Responsibilities

• Contribute to clinical development plans and study design.
• Support development of protocols, amendments, and informed consent documents.
• 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.
• Participate in investigator meetings and site engagement activities.
• Support identification and resolution of study issues.
• Review safety, efficacy, biomarker, and PK/PD data.
• Identify data trends and quality concerns.
• Collaborate on database lock and analysis activities.
• Support interpretation of study results.
• Prepare and review clinical study reports, abstracts, and presentations.
• Support advisory boards and scientific congress activities.
• Contribute to Investigator’s Brochures and regulatory submissions.

Benefits

• Competitive salary
• Annual bonus based on company performance
• Healthcare and wellbeing programs
• Pension plan membership
• Shares and savings programme
• Health care and other insurance benefits for employees and family
• Retirement benefits
• Paid holidays
• Vacation
• Paid caregiver, parental, and medical leave
• Eligibility to participate in a share-based long-term incentive program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree