Site Engagement Associate Director - Respiratory

gsk; United States; Remote; USD 130,000 - 216,000; Full time

Benefits offered by this job

Health care benefits

Retirement benefits

Paid holidays

Vacation

Parental and medical leave

Job summary

GSK in the United States seeks an Associate Director Site Engagement to lead strategic site partnerships, manage cross-functional interfaces, and optimize the clinical trials environment for timely, high-quality outcomes.

You will drive network expansion across academic centers and community sites, ensure KPI-driven performance, and collaborate with LOC/MED to deploy digital tools and improve site performance.

Qualifications

• Bachelor’s degree in life science or equivalent experience.
• 5+ years’ experience in clinical research operations.

Responsibilities

• Conduct strategic environmental surveillance to anticipate regulatory and operational changes affecting sites and R&D in the United States.
• Contribute to development of a strategic partnership network between GSK and sites.
• Lead development and expansion of a US site network spanning academic centers, community practices, and hybrid networks.
• Provide feedback to Leadership, Local Medical Affairs, LOC on partnerships and updates.
• Drive KPI targets and conduct performance reviews with external partners to improve cycle times and enrolment.
• Identify bottlenecks at study and site levels; develop mitigation plans to ensure quality and compliance.
• Collaborate with Feasibility, Clinical Operations, and Medical Affairs for optimal site placement and study performance.
• Drive adoption of digital and centralized solutions (eConsent, eReg, remote SIVs, EMR-based ID and monitoring).
• Offer strategic input for operational excellence and process efficiency across LOC/region/global networks.
• Develop unique site models to broaden the portfolio of sites in studies.

Skills

Agile Thinking

Business Acumen

Clinical Development

Clinical Trial Designs

Communication

Creativity

Decision Making

Fostering Collaboration

GCP

Influencing Without Authority

People Management

Pharmaceutical Industry

Project Management

Time Management

Education

Bachelor’s degree in life science or equivalent experience

Job description

Through leadership, the Associate Director Site Engagement is accountable for developing, managing, and overseeing long-term and strong relationships with strategically and operationally important Oncology sites and institutions. It includes building and enhancing the image and reputation of GSK with sites locally and providing an interface between GSK and the sites to create an optimal clinical trials environment to generate results in a timely manner with high quality outputs.

Responsibilitiesinclude:

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

• Conduct strategic environmental surveillance to anticipate regulatory and operational changes affecting sites and R&D in the United States, and use those insights to design innovative, efficient partnerships.

• Contribute to the development of a strategic partnership network, acting as the main point of contact between GSK and sites:in the Network SEL willidentifyexternal organizations / institutions and evaluate their interest to build and develop networks with GSK on a local basis.

• Lead the development and expansion of a US site network spanning academic centers, community practices, and emerging site model (hybrid networks, DCT enabled sites.

• Provide feedback to Leadership, Local Medical Affairs, LOC regarding the development of new partnerships and updates on existing ones

• Drive performance, by putting in place mutually agreed KPI targets (quality and performance) and organizing regular, periodic performance reviews with the different external partners track compliance with mutually agreed action plans, implementing targeted solutions to reduce cycle times across the study lifecycle and optimize enrolment; participate in/lead site visits to deliver targeted operational support and address site-specific challenges.

• Work closely with sites and with all members of the LOC Clinical Operations Department to proactivelyidentifybottlenecks at both the study and site level and any risks to quality and compliance and to develop and implement mitigation plans to address these risks, supporting corrective actions to ensure successful outcomes

• Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance

• Drive adoption of enterprise and other digital and centralized solutions (e.g., eConsent, eReg, remote SIVs, EMR- based identification and remote EMR monitoring access)

• Conduct an ongoing environmental strategic surveillance andanticipate the legislative and practical evolution of sites and R&D in the country and use those insights to design and curate innovative and efficient partnerships.

• Give an operational vision of the future GSK clinical research therapeutic areas and GSK portfolio (collaborating with Local Medical Affairs (LOC MED)) to key external stakeholders toanticipatepartnerships and to help research institutions and sites better prepare the arrival of clinical trials.

• Provide strategic input for operational excellence, processefficiencyand trial delivery both internally and externally; identifyand share best practices at internal cross functional process improvement teams, contributing to efficient and consistent ways of working to optimizing quality and productivity across LOC / region / global site network as appropriate.

• Consider and develop unique site models, further enhancing portfolio of sites to include in studies

Why You?

Basic Qualifications

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

• Bachelor’s degree in life science or equivalent experience

• 5+ years’ experience in clinical research operations

Preferred Experience

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

• Ability to travel up to 60% (Domestic)

• Experience in respiratory and/or hepatology.

• Proficient knowledge of the Drug Development Process

• Excellent understanding of the Clinical Study Process, including monitoring

• Demonstrated track record of establishing and growing partnerships with strategic sites / institutions

#LI-Remote

Skills

• Agile Thinking
• Business Acumen
• Clinical Development
• Clinical Trial Designs
• Communication
• Creativity
• Decision Making
• Fostering Collaboration
• Good Clinical Practice (GCP)
• Influencing Without Authority
• People Management
• Pharmaceutical Industry
• Project Management
• Time Management

The US annual base salary for new hires in this position ranges from $129,750 to $216,250. 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. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

• health care and other insurance benefits (for employee and family)
• retirement benefits
• paid holidays
• vacation
• paid caregiver/parental and medical leave

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 we’re 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.

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