Director Clinical Sciences, Oncology

MedStar Health; Collegeville (PA); On-site; USD 130,000 - 190,000; Full time

Job summary

A global biopharma company seeks a Director of Clinical Sciences to lead oncology development strategies. This pivotal role involves managing teams, driving clinical strategy, and ensuring product efficacy while maintaining high-quality standards in clinical development. The ideal candidate will demonstrate a strong background in oncology and project management, alongside effective leadership and communication skills.

Qualifications

• Minimum of 5 years relevant experience in the pharmaceutical industry.
• Oncology experience is preferred.
• Experience leading teams with progressively senior positions.

Responsibilities

• Develop and lead oncology strategies for product launches.
• Oversee the clinical development activities for regulatory approvals.
• Integrate and analyze data for strategic decisions.

Skills

Leadership

Project Management

Clinical Development

Communication

Team Management

Education

PhD

Job description

Site Name: USA - Pennsylvania - Upper Providence, Cambridge MA
Posted Date: Jun 20 2025

Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you!

As the Director Clinical Sciences, Oncology, you will be responsible for building up the current Oncology development team, including recruitment of clinical scientists, and developing and leading GSK medium and long-term oncology development strategies for GSK's oncology pipeline. You will work closely with the Global Oncology Research and Development and Medical Affairs to ensure that the oncology clinical team have the highest quality capabilities and expertise. You will also ensure the optimal launch of new products and appropriate optimal patient use of currently available GSK Medicines through leadership and collaboration.

In this role you will:

• Ensure delivery of quality study strategy and design, understand the analysis and interpretation of data throughout the study.
• Lead or contribute, as appropriate, to the end to end (protocol concept to final study report) delivery of clinical development activities which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into strategic and operational decisions.
• Understand the asset's biological mechanism, clinical strategy, scientific interpretation of disease and target-based literature.
• Integrate data from internal, and external academic, conference and competitor sources. Appropriately interact with Key External Experts (KEEs), Key Opinion Leaders (KOLs), collaborators, advisory boards, etc.
• Implement new business processes and strategies and may also proactively identify issues and propose strategies to manage implications and risks on clinical study/Clinical Development plan (CDP). Ensure the high quality of protocol documents are developed aligned to the CDP to effectively determine a medicine's potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe.
• Drive/contribute to clinical components of the IB, and documents for regulatory submissions and advisory requirement, including scientific advice, IND, EoP2, pre-NDA/BLA meetings, NDA/BLA and MAA documents.

Why you?

Basic Qualifications:

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

• PhD is required
• Minimum of 5 years relevant experience

Preferred Qualifications:

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

• Oncology experience preferred.
• Experience in the Pharmaceutical industry with specific experience leading a team with progressively more senior positions and responsibility
• Experience in clinical development
• Project Management experience
• Experience and understanding of the drug development, regulatory and commercialization process, including clinical trial development, is critical to the role
• Strong communication skills appropriate to the target audience, promoting effective decision-making where necessary. Good leadership and influencing skills.
• Knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution
• Knowledge of worldwide regulatory and safety requirements as pertains to drug development, research projects, and/or market support.
• Experience managing, developing and motivating a team to deliver results in a timely manner
• Ability to identify, hire, and coach talent to improve performance
• Experience in change management, restructuring, and building capabilities
• Strong team leadership skills in line management and matrix environments
• Experience identifying, assessing and understanding the needs of key decision makers and stakeholders and building effective relationships in a matrixed environment
• Experience in setting high performance standards and measures, driving accountability throughout the function and mentoring staff

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:

• Agile and distributed decision-making - using evidence and applying judgement to balance pace, rigour and risk
• Managing individual and team performance.
• Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
• Implementing change initiatives and leading change.
• Sustaining energy and well-being, building resilience in teams.
• Continuously looking for opportunities to learn, build skills and share learning both internally and externally.
• Developing people and building a talent pipeline.
• Translating strategy into action - a compelling narrative, motivating others, setting objectives and delegation.
• Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally.
• Budgeting and forecasting, commercial and financial acumen.

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 special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or [phone] (outside US).

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 GSK's 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 GSK. In 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 GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/