Clinical Scientist, Hepatology Clinical Development

GSK; United States; On-site; USD 151,000 - 252,000; Full time

Benefits offered by this job

Annual bonus based on company perfomrn

Healthcare and wellbeing programs

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 hepatology studies. You will collaborate with Medical Monitoring, Clinical Operations, Biostatistics, and external investigators to deliver high-quality data.

On-site work is required in the US or UK, with strict limits on remote or hybrid options. The role emphasizes protocol development, safety oversight, data interpretation, and regulatory submission support, including

Qualifications

• Minimum of a PharmD, PhD, MD, or equivalent.
• A minimum of 3 years of clinical research or drug development experience.
• Demonstrated ability to work effectively in cross-functional teams and with external partners.

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.
• 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 Investor's Brochures and regulatory submissions.

Skills

Agile Thinking

Clinical Development

Clinical Trial Designs

Decision Making

Fostering Collaboration

Influencing Without Authority

Leadership

Matrix Leadership

Mentorship

People Management

Project Management

Risk Management

Strategic Thinking

Teamwork

Time Management

Education

Minimum of a PharmD, PhD, MD, or equivalent

Job description

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a remote or hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company-wide benefits and life at GSK on our webpage Life at GSK | GSK

Find out more about GSK and R&D: Our approach to R&D

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 Investor's Brochures and regulatory submissions.

Basic Qualifications

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

Preferred Qualifications

• 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.

Skills

• Agile Thinking
• Clinical Development
• Clinical Trial Designs
• Decision Making
• Fostering Collaboration
• Influencing Without Authority
• Leadership
• Matrix Leadership
• Mentorship
• People Management
• Project Management
• Risk Management
• Strategic Thinking
• Teamwork
• Time Management

Benefits

If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $150,975 to $251,625. The US salary ranges take into account a number of factors including work location within the US market, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and v