ppSalary Range: €46,300.00 - €86,100.00 Band Level 4 Job Description Summary #LI-Hybrid This role is based in our Barcelona Gran Via, Spain office, with a Hybrid working expectation of 12 days per month onsite. Relocation support is not provided for these positions. Please note that we are also hiring for these positions in Dublin, Ireland; London, UK and East Hanover, NJ, USA, all on a Hybrid working basis. Novartis cannot sponsor Visas for this location. /ph3Job Description /h3pAre you energized by the opportunity to shape clinical data strategy across complex trials and help deliver high-quality, submission-ready data that supports faster, better decisions for patients? As a Clinical Study Data Lead within Clinical Data Operations, Global Clinical Operations, you will serve as a trusted data strategy partner to Clinical Trial Teams and cross-functional stakeholders, bringing clarity, consistency, and accountability to end-to-end clinical data delivery across multiple trials. /ph3Who Will Thrive in This Role /h3pThis opportunity is well suited for an experienced clinical data management professional with strong operational leadership, sound judgment under pressure, and the ability to influence cross-functional teams. The adecuado candidate brings deep understanding of clinical trial methodology, Good Clinical Practice, data standards, regulatory expectations, and hands‑on trial‑level data delivery—typically gained through proven experience in clinical data management within a regulated RD environment. If you are ready to bring strategic data leadership, operational discipline, and a quality‑first mindset to complex clinical trials, this role offers the opportunity to make a meaningful contribution to predictable delivery, inspection readiness, and high‑quality clinical data outcomes across the portfolio. /ph3What You’ll Contribute /h3ulliLead clinical data management activities across multiple assigned trials, ensuring high-quality, timely, and compliant data outputs. /liliDefine and drive trial‑level data strategies aligned with program objectives, data standards, and regulatory expectations. /liliOversee end‑to‑end data management from data collection and database design through data cleaning, review, and database lock readiness. /liliRepresent Clinical Data Management in Clinical Trial Team and Data Quality Team forums, influencing decisions and resolving data topics with clarity and urgency. /liliIdentify and manage data risks, dependencies, and cross‑trial issues through proactive mitigation, root cause analysis, and timely escalation where needed. /liliReinforce Quality by Design, audit readiness, and consistent application of standards and processes across assigned trials. /liliShare insights, lessons learned,



and practical guidance to strengthen decision‑making and continuous improvement across the trial portfolio. /li /ulh3What Differentiates This Role /h3ulliSingle point of accountability: you will own end‑to‑end clinical data strategy and delivery across multiple trials, creating consistency and predictability across the portfolio. /liliStrategic influence with hands‑on impact: the role combines operational execution with data‑driven decision‑making in governance forums where clinical data topics are shaped and resolved. /liliCross‑functional leadership without direct reports: you will coordinate resources, influence stakeholders, and guide Principal Study Data Leads through expertise, partnership, and credibility. /liliDirect contribution from protocol development to submissions: your work supports data‑specific inputs to the protocol, set up of high‑quality dataflows, smooth database locks and timely Health Authority submissions, making the role critical to program delivery and patient impact. /liliInspection‑ready mindset: the position places strong emphasis on quality, compliance, standards, proactive risk management, and regulatory expectations. /li /ulh3Essential Requirements /h3ulliBachelor’s degree, or equivalent, in life sciences, computer science, or a related field. /liliPostgraduate qualification in a relevant field is beneficial. /liliProven experience managing clinical trial data and driving clinical data strategy and execution across multiple studies and delivering to deadlines. /liliIdeally a minimum of 5‑8 years' experience in clinical data management. /liliStrong knowledge of clinical trial methodology, good clinical practice (GCP), and medical terminology. /liliAdvanced ability to analyze and interpret data and apply critical thinking, and make data driven decisions. /liliDemonstrated leadership and collaboration skills in cross‑functional, global team environments. /liliAbility to identify risks, solve complex problems, and implement effective data management solutions. /liliExcellent communication skills, with ability to influence stakeholders across functions and organizations. /liliExperience mentoring colleagues and sharing knowledge to support team and project success. /li /ulh3Benefits Rewards /h3pExpected Annual Base Salary Range for role: €46,300.00 - €86,100.00 Annual.



/ppThe base salary offered is determined based on gender‑neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. /ppIn addition to your base salary, you may be eligible for a performance‑based bonus depending on certain performance parameters. /ppThe rewards of being part of our team go far beyond base pay and incentives. /pulliinsurance plans /liliretirement plans /liliwellbeing resources /liliglobal recognition programs /liliflexible and hybrid working options /liliminimum 14 weeks paid parental leave /li /ulpPay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. /ppRead our brochure to learn more about our global total rewards offering: /ppNote: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. /ppA full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. /ph3Commitment to Diversity and Inclusion / EEO /h3pNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /ppYou’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. /ppCommitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /ph3Skills Desired /h3ulliClinical Data /liliClinical Data Analysis /liliClinical Data Management /liliClinical Research /liliClinical Studies /liliData Analysis /liliData Analytics /liliData Architecture Development /liliData Governance /liliData Integration /liliData Management /liliData Profiling /liliData Quality /liliData Science /liliGood Clinical Data Management Practice (GCDMP) /liliMaster Data /liliStatistical Analysis /liliWaterfall Model /li /ulpImproving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. /p /p #J-18808-Ljbffr

📌 Clinical Study Data Lead - Barcelona (Sabadell)
🏢 ES06 (FCRS = ES006) Novartis Farmacéutica
📍 Sabadell