Clinical Research jobs in United States

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 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. GSK has kicked off 2025 with impressive growth in sales profits and earnings. We anticipate five major new FDA product approvals and 15 phase III / pivotal study readouts over the next two years. So far we have secured two FDA approvals with three more expected later this year. By uniting science technology and talent we are committed to getting ahead of disease together.

The Clinical Operations Asset Lead represents all Clinical Operations functions at the asset level and is accountable for developing the operational strategy and delivery plan to execute the scientific strategy for an asset and associated studies working in partnership with clinical / biostats / clinical supplies and the functional subject matter experts to ensure informed asset decision‑making from the operational scientific and data perspectives.

• Contribute to the development of the Clinical Development Plan and Integrated Evidence Plan during Research Development phases of the asset lifecycle.
• Provide input into the overarching Clinical Development Plan and the development of studies that align to the Clinical Development Plan and are feasible to implement in the clinical and regulatory environment of participating regions to provide quality data and ensure timely study delivery coordinating expert inputs from clinical and non‑clinical functions.
• Utilize lessons learnt and prior experiences to ensure best practices and strategies.
• Be part of the protocol development finalization and subsequent amendments including relevant review boards / committees to ensure operational feasibility and consistency within the asset.
• Lead resourcing discussions and be accountable for the final strategy (in vs outsourcing) for the asset and studies in accordance with the resourcing strategy & principles.
• Approve / endorse assessment selection contracting and management of appropriate vendors for outsourced clinical activities and services ensuring compliance with GSK standards.
• Lead escalation point from study and asset level to raise and assist with issues on behalf of the team including serious quality incidents and serious breaches of GCP.
• Responsible for the coordination and leadership of cross‑functional team input into development plans ensuring quality delivery of all studies included within the plans.
• Ensure clinical operations inspection readiness at all times and supports preparations in the event that any studies within the asset is subject to inspection.
• Ensure regular interaction with clinical operations functions involved in the asset such that they are aware of issues risks and successes with study delivery as they occur.
• For outsourced programs coordinate oversight to ensure the quality delivery by provider.
• Model scenarios for optimal asset / study delivery linked to value drivers and drives decisions presented to governance boards to optimise delivery with transparent implications to time quality risks resources and budget.
• Accountable for the operational planning feasibility and delivery of their assigned asset(s) and associated Development Plan(s) on time and on budget from beginning to end whilst optimizing time and cost efficiency including resource utilisation.
• Drive innovative approaches to study execution through external facing advances in technology and sciences by identifying and embracing risks and opportunity.
• Accountable for asset delivery strategy (e.g. country diversity patient engagement strategies etc) in collaboration with cross‑functional stakeholders with particular accountability for Clinical Operations contributions to governance boards.
• Accountable for budget forecasts for future interventional clinical and Epi studies and Clinical Operations asset level costs ensuring they are accurately represented and managed in financial tools.
• Ensure clinical operational delivery with a collaborative partner in a co‑development environment.
• Contribute to the clinical file submission team by coordinating deliveries linked to interventional clinical and Epi studies and responses to questions raised by Health Authorities on operational activities. Deliver applicable operational modules for the file.
• Ensure asset level operational risk management plan is in‑place and applies a smart‑risk taking philosophy.
• Accountable for asset level mitigation plans are implemented to avoid and manage risk / quality issues.
• Accountable for translating technical content to ensure appropriate operational implementation at the study level.
• Manages internal and external stakeholders through appropriate engagement and communication.
• Accountable for all data related to delivery strategy (e.g. country footprint resourcing strategy) is accurate and contemporaneous in GSK systems (including clinical trial tracking systems).

• Demonstrates conceptual analytical and strategic thinking to innovative approaches to clinical delivery leverage external technology and networks and build internal capability.
• Ability to translate strategic concepts scientific requirements stakeholder feedback and expectations into cohesive actions for the Asset team.
• Ability to define value‑driven vision and roadmap for the Clinical and or Epi Development Plan.
• To be an external advocate representing GSK at congresses industry bodies or other external opportunities.
• Ability to represent the function in change initiatives or SME roles embracing and promoting GSKs values and culture.
• Ability to effectively prioritize activities and stakeholder needs whilst balancing the broader business needs with the needs of their specific asset.
• Competent in working with complexity and uncertainty within the external regulatory environment (e.g. FDA EMEA).
• Innovative and change adept whilst identifying and embracing risks as opportunities.
• Ability to establish and build internal and external relationships at all levels in a highly dynamic and matrixed environment demonstrating conflict management and negotiation skills.
• Partnering skills with key role such as clinical science biostatistics and other subject matter experts (SME) at asset level to articulate and champion key decisions and strategy.
• Excellent leadership skills building and managing matrixed teams promoting motivation and empowerment of others to accomplish individual team and organisational objectives.
• Excellent influencing and stakeholder management skills at all levels of the organisation.
• Highly developed communication skills appropriate to the target audience promoting effective decision‑making.
• Leadership style and resource alignments sensitive to different cultures and experience levels in a matrix environment to ensure appropriate asset operational delivery and optimally motivate individuals to reach their potential.

• Bachelors degree in general science or a Life / Health‑related discipline.
• Proven expertise in managing complex clinical research projects across multiple phases and geographies.
• Demonstrated experience in oncology clinical operations with a strong track record of delivering high‑impact outcomes.
• Established leadership in above‑study roles including strategic oversight and cross‑functional coordination.
• Hands‑on experience in delivering registrational oncology studies supporting regulatory inspections and contributing to regulatory submissions.
• Deep knowledge of clinical development processes and matrix management within global organisations.
• Recognised leadership capabilities and ability to influence senior stakeholders effectively.
• High adaptability and versatility evidenced by contributions across diverse roles disciplines and therapeutic areas.

• Advanced proficiency in oncology clinical operations with a history of driving innovation and excellence.
• Masters degree or equivalent experience in Pharmacy Chemistry Bioengineering Biology Biomedical Sciences Project Management or Business Administration.

Employee Relations, Employee Evaluation, Management Experience, Profit & Loss, Conflict Management, Operations Management, Project Management, Budgeting, Leadership Experience, Supervising Experience, Leadership management, Financial Planning

Employment Type: Full‑Time

Experience: years

Vacancy: 1

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.

We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or 0. The helpline is available from 8.30am to 12.00 noon Monday to Friday during bank holidays these times and days may vary.

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.

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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.