Overview
Local Study Manager role at GSK – Verona, Italy.
Site Name: Italy - Verona
Posted Date: Oct 29 2025
We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK
Scope
For our headquarters in Verona, we are looking for a Local Delivery Lead to be included in our Clinical Operations area. The role is initially allocated to the Oncology therapeutic area, with the possibility of involvement in other therapeutic areas within Clinical Operations (such as vaccines, infectious diseases and others).
Responsibilities
The Local Delivery Lead (LDL) is the lead for within-country operational feasibility, planning and delivery of Phase I-IV clinical trials and epidemiological and Health Outcome studies in a specific country or cluster of countries. They are accountable for within-country execution and delivery of assigned studies to time, budget and quality expectations as defined in the clinical development plan and study protocol, as well as in local regulations, IND/GCP/ICH-guidelines, GSK Corporate and local SOPs and POLs. Their scope includes matrix leadership and project management of country and site-level activities oversight including site management & monitoring. The LDL serves as the operational point-of-contact between the central Study Delivery Lead and in-country operational staff. They collaborate with local medical staff, Clinical Research Associates (CRA)/monitors and other in-country staff.
Qualifications
Basic Qualifications & Skills
* University Scientific Degree or equivalent qualification (Pharmacy, Chemistry, Bio Engineering, Biology, Biomedical Sciences, Nursing etc).
* 3 years of previous Clinical Operations experience with at least 2 years of in-country monitoring or study management experience or equivalent.
* Demonstrated high level of understanding of clinical research and clinical trial management, and the associated regulatory, processes and quality requirements.
* Self-motivated with the ability to work independently and proactively, to develop credibility with colleagues within and outside Clin Ops team, and to influence decisions.
* Excellent understanding of Clin Ops strategy and purpose in the pharmaceutical industry and ability to translate scientific knowledge into business-driven strategies/activities.
* Internal and external customer focused and oriented.
* Fluent Italian and English.
Preferred Qualifications & Skills
Note: The following skills are preferred but not required; if you do not have them, please still apply.
* Proven leadership skills in motivating and empowering teams to achieve organizational goals.
* Strong expertise in clinical study processes, drug development, sample management, and quality requirements.
* Skilled in project management, including scope, budget, timeline, resource planning, and financial reporting.
* Collaborative leader with the ability to work across functional and geographical boundaries, fostering communication and teamwork.
* Proficient in setting priorities, managing resources, and achieving performance targets in local/regional settings.
* Experienced in risk management, contingency planning, and applying industry best practices for efficient clinical study execution.
What We Offer
* Permanent contract in a very Inclusive environment
* Performance Reward
* Flexible Benefits
* Company Healthcare Plan
* Integrative pension fund
* Employee Assistance Programme
* Tax assistance
* Personal parcel delivery service
* Local nursery agreement
* Free Company canteen
* Coffee Corners
Application Details
Closing Date for Applications: 11/11/2025
Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.
Why GSK?
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. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases.
We are committed to creating an environment where our people can thrive and focus on what matters most. Our culture emphasizes being ambitious for patients, accountable for impact and doing the right thing. 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).
Equal Opportunity Employer
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, military service or any basis prohibited under federal, state or local law.
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Notes
Seniority level: Not Applicable
Employment type: Full-time
Job function: Research, Analyst, and Information Technology; Industries: Pharmaceutical Manufacturing
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