Clinical Scientist, Hepatology Clinical Development Full-time

Clinical Scientist, Hepatology Clinical Development

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

This role can be in either Waltham, MA in the US or GSK Headquarters in London, UK and requires working on-site. Hybrid or remote work options are not available for this position.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• 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.
• Participate in investigator meetings and site engagement activities.
• Support issue identification and resolution.
• Review safety, efficacy, biomarker, and PK/PD data.
• Identify trends and data quality concerns.
• Collaborate on database lock and analysis activities.
• Support interpretation of study results.
• Prepare and review CSRs, abstracts, and presentations.
• Support advisory boards and scientific congress activities.
• Contribute to Investigator's Brochures and regulatory submissions.

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

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

Preferred Qualifications:

Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:

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

Join us in making a difference in patients' lives around the world. We value your unique perspective and invite all interested candidates to submit their application.