Clinical Data Strategy Lead – Hybrid, Impactful Trials

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.; Sabadell; Hybride; EUR 46 000 - 86 000; Plein temps

Avantages offerts par ce poste

Hybrid working options

Wellbeing resources

Parental leave (14 weeks)?

Insurance plans

Retirement plans

Global recognition programs

Résumé du poste

Novartis Farmacéutica, S.A. in Barcelona is seeking a Clinical Study Data Lead to champion end‑to‑end data strategy across trials. You will lead data management activities, define trial data standards, and ensure timely, compliant outcomes in a hybrid setting.

The role requires 5–8 years in clinical data management, strong GCP knowledge, and ability to influence cross‑functional teams. Visa sponsorship is not provided for this location. This is a hybrid role with 12 onsite days per month.

Qualifications

• Bachelor’s degree, or equivalent, in life sciences, computer science, or a related field.
• Postgraduate qualification in a relevant field is beneficial.
• Proven experience managing clinical trial data and driving clinical data strategy and execution across multiple studies and delivering to deadlines.
• Ideally a minimum of 5-8 years' experience in clinical data management.
• Strong knowledge of clinical trial methodology, good clinical practice (GCP), and medical terminology.
• Advanced ability to analyze and interpret data and apply critical thinking, and make data driven decisions.
• Demonstrated leadership and collaboration skills in cross‑functional, global team environments.
• Ability to identify risks, solve complex problems, and implement effective data management solutions.
• Excellent communication skills, with ability to influence stakeholders across functions and organizations.
• Experience mentoring colleagues and sharing knowledge to support team and project success.

Responsabilités

• Lead clinical data management activities across multiple assigned trials, ensuring high‑quality, timely, and compliant data outputs.
• Define and drive trial‑level data strategies aligned with program objectives, data standards, and regulatory expectations.
• Oversee end‑to‑end data management from data collection and database design through data cleaning, review, and database lock readiness.
• Represent Clinical Data Management in Clinical Trial Team and Data Quality Team forums, influencing decisions and resolving data topics with clarity and urgency.
• Identify and manage data risks, dependencies, and cross‑trial issues through proactive mitigation, root cause analysis, and timely escalation where needed.
• Reinforce Quality by Design, audit readiness, and consistent application of standards and processes across assigned trials.
• Share insights, lessons learned, and practical guidance to strengthen decision‑making and continuous improvement across the trial portfolio.

Connaissances

Clinical Data Management

Cross-functional leadership

GCP

Data Standards

Data Analysis

Regulatory compliance

Formation

Bachelor’s degree in life sciences or related field

Postgraduate qualification

Description du poste

Novartis Farmacéutica, S.A. in Barcelona is seeking a Clinical Study Data Lead to champion end‑to‑end data strategy across trials. You will lead data management activities, define trial data standards, and ensure timely, compliant outcomes in a hybrid setting.

The role requires 5–8 years in clinical data management, strong GCP knowledge, and ability to influence cross‑functional teams. Visa sponsorship is not provided for this location. This is a hybrid role with 12 onsite days per month.