Job description Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK – London – New Oxford Street, USA - District of Columbia - Washington Dc, USA - Massachusetts - Waltham Posted Date: Nov 14 2024 GSK is a global healthcare company committed to improving the quality of human life by enabling people to do more, feel better, and live longer.
We discover, develop, and deliver innovative medicines, vaccines, and consumer healthcare products, and we are dedicated to our mission of helping people around the world.
At GSK, we are dedicated to creating an inclusive and diverse workplace that reflects the communities we serve.
We offer competitive compensation and benefits packages, opportunities for professional development, and a culture that values innovation, collaboration, and integrity.
The Scienti st , Interventional Studies will oversee the execution of a program of sponsored clinical trials by the medical affairs organization (non - regulatory label directed programs) .
This role requires a manager with expertise in industry sponsored clinical research & global medical affairs and have good cross-functional team management.
The scientist will ensure that all interventional studies under their scope are conducted to the highest standards of quality, ethics, and efficiency, utilizing the latest clinical trial innovations including digital health , driving forward GSK's pipeline of innovative therapeutics.
They will work in a matrix manner with the Global Medical Affairs therapy area teams, and the clinical operation & Biostatistics organization to execute the program of work.
Key Responsibilities: Operational Management: Oversee the operational aspects (delivered by clinical operations & Biostatistics) of medical affairs interventional studies, including planning, budgeting, resource allocation, and timeline management.
Collaborate with cross-functional R&D teams to ensure seamless execution and delivery of clinical program s, as well as third party vendors.
Monitor and manage study progress, ensuring compliance with protocols, regulatory requirements, and GSK standards.
Regulatory and Compliance: Ensure that all interventional studies are conducted in accordance with GCP, and other relevant regulatory guidelines.
Maintain oversight of all regulatory submissions and interactions related to interventional studies.
Ensure robust quality control and assurance processes are in place for all clinical trials.
Stakeholder Engagement: Serve as the primary point of contact for internal and external stakeholders regarding interventional studies.
Collaborate with key opinion leaders, investigators, and external partners to enhance study design and execution.
Communicate study progress, challenges, and outcomes to senior leadership and other relevant stakeholders.
Innovation and Continuous Improvement: Identify and implement innovative approaches to improve the efficiency and effectiveness of interventional studies.
S tay abreast of industry trends, emerging technologies, and new methodologies in clinical research.
Promote a culture of continuous improvement within the interventional studies team.
Why you?
Basic Qualifications : We are looking for professionals with these required skills to achieve our goals: Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
Minimum of 1 0 years of experience in clinical research Proven track record of successful management of large-scale interventional clinical trials.
In-depth knowledge of regulatory requirements and industry standards for clinical research , including being a medical monitor.
Preferred Qualifications: If you have the following characteristics, it would be a plus: Good leadership, communication, and interpersonal skills.
Strong problem-solving abilities.
Ability to thrive in a fast-paced, dynamic environment and manage multiple priorities.
? Please visit GSK US Benefits Summary t o 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 +1 801 567 5155 (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles.
This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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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.
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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 GSK's Transparency Reporting For the Record site.
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