Clinical Development Medical Director – Renal

At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples lives. GSK fosters a culture ambitious for patients accountable for impact and committed to doing the right thing making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science technology and talent to get ahead of disease together.
Find out more:
Our approach to R&D


Position Summary
You will lead clinical development for renal medicine programs in a collaborative and patient-focused setting. You will shape clinical strategies design studies and guide clinical teams to make data-driven decisions. We value clear communication scientific curiosity and teamwork. This role offers growth the chance to impact patients lives and alignment with GSKs mission of uniting science technology and talent to get ahead of disease together.

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

- Lead design and execution of clinical development plans and protocols for renal programs across early and later phase studies.
- Provide medical governance and safety oversight for clinical trials working closely with pharmacovigilance and clinical operations.
- Serve as clinical lead in cross-functional project teams and as a key medical contact for internal and external stakeholders.
- Translate clinical and translational science into study endpoints biomarker strategies and go/no-go decision points.
- Support regulatory interactions and contribute to regulatory documents and responses.
- Build and maintain relationships with investigators key opinion leaders and patient groups to inform study design and evidence generation.
- Provide clinical leadership for renal development programs from early proof-of-concept to later phase studies.
- Contribute to protocol development investigator materials study reports and clinical documents.
- Ensure high standards for patient safety and medical governance throughout study conduct.
- Integrate input from translational science biostatistics regulatory and commercial teams into clinical plans.
- Oversee medical monitoring activities and ensure timely medical input into operational study decisions.
- Mentor colleagues and share clinical expertise to develop capability within the team.

Why You

Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

- Medical degree (MD DO MBBS or equivalent) from an accredited institution.
- Completion of clinical residency and appropriate specialty training ideally including nephrology experience.
- Minimum 3 years clinical research experience in drug development or clinical trials.
- Experience leading or providing medical input to clinical study design and execution.
- Understanding of clinical trial regulations and Good Clinical Practice.
- Strong collaboration skills and experience working in cross-functional or matrix teams.

Preferred Qualifications:
If you have the following characteristics it would be a plus:

- Board certification or specialist qualification in nephrology.
- Experience with translational biomarkers and patient stratification in renal disease.
- Prior experience with global clinical trials and interactions with regulatory agencies.
- Experience in protocol medical monitoring or pharmacovigilance collaboration.
- Track record of publications or presentations in renal medicine or clinical research.
- Experience mentoring clinicians or leading clinical project teams.

What you can expect from us
You will join a team that values inclusion patient focus and scientific integrity. We offer a collaborative environment where your clinical expertise influences development decisions. You will gain opportunities to grow professionally while contributing to meaningful work that advances care for people with kidney disease.

We encourage you to apply if you are ready to bring clinical leadership curiosity and a collaborative mindset to a team working to make a real difference for patients. Apply now and help us get ahead of disease together.

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 vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

Please note should your inquiry not relate to adjustments we will not be able to support you through these channels. However we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license GSK may be required to capture and report expenses GSK incurs on your behalf in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Experience:

Director