Clinical Trials Expert

Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement.

Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.

La position In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary life‑changing innovation at speed.

Strategy, Portfolio & Operations (SPO) is a unified function that serves as the strategic and operational backbone enabling pRED's strategy from lab to clinic. Operating under a dynamic Chapter Model, SPO centralises specialised skills across critical areas including Sites & Lab Services, Program & Project Management, Strategy, Clinical Operations, External Operations, Capability Development, Core Lab Technology Platforms (360Labs) and Asset Team Leadership. SPO’s mission is to drive enterprise value creation by delivering operational excellence and accelerating portfolio productivity.

As a trusted partner, SPO fosters a culture of collaboration and accountability to ensure pRED transitions assets smoothly from early research to late‑stage development.

At Roche Pharma Research and Early Development Clinical Operations (pRED CO), we are determined to transform early drug development and realise our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029.

As part of the CO Community, the Clinical Trial Expert is accountable for a range of end to end study‑level activities from systems set up to close out during the execution of trial(s). S/he is responsible for the delivery of operational systems and technical activities (e.g. eCOA, IxRS) in support of the Study and Programme delivery within timelines, budget, quality, while contributing towards the CO North Star of improving productivity and approaching study delivery from a patient centric mindset.

The Postholder is accountable for delivering strategic components within their area of expertise that improve CO’s productivity metrics. The role also requires enterprise‑wide interconnectivity, networking, and monitoring of the internal and external environments.

In this position you will:

• Ensure the Clinical Operations organisation achieves and maintains a sustainable high level of portfolio delivery performance by implementing and maintaining study‑specific solutions that deliver on the CO goals and objectives in your domain of expertise (e.g. IxRS, eCOA).
• Lead the implementation of systems maintenance, tools and reports required across the clinical trial life cycle (eCOA, IxRS, etc).
• Coordinate components of study startup, including input into / ownership of requests for proposal, authoring of documents and potentially site personnel training.
• With a strong background in trial system implementation and execution, you contribute to specific study strategies pertaining to your domain of expertise.
• Establish and maintain optimal relationships with key internal and external partners and stakeholder groups.
• Contribute to the development and maintenance of relevant study oversight documentations/charters, processes and best practices as needed and represent pRED at cross‑enterprise CO forums.
• In your relevant domain of expertise, track study progress and address issues that may come up in close collaboration with study teams, affiliates, sites, and CROs as appropriate.
• Collaborate with stakeholders in generating relevant reports and KPIs to monitor trial progress.
• Identify signals and systematic areas for improvement at an Enterprise level.
• Establish standard approaches and provide support across the clinical portfolio in a range of activities such as Training Materials, Processes, SOPs, etc.

Who You Are

You are talented, passionate, and inspired by our mission, fitting perfectly into our collaborative, patient‑centric, and entrepreneurial spirit; you want to make a difference and find excitement in innovating practices, therapeutics, and processes.

You hold a university degree (or equivalent experience, preferably in life sciences) and possess deep experience in the pharmaceutical/healthcare industry and drug development (therapeutic area a plus), alongside a solid understanding of the clinical trial environment, ICH‑GCP, and lifecycle sequence/interdependencies.

You are highly experienced in clinical trial management tools, systems, and their interdependencies, specifically including IxRS, eCOA, centralised endpoint review (such as images, ECG, etc.), and digital biomarkers.

You possess a solid grounding in business performance improvement methodologies—including project conceptualisation, situational analysis, solution design, implementation, and continuous improvement—and have the ability to collaborate with a range of stakeholders to implement the strategic direction for early development clinical studies.

You find passion in achieving successful outcomes by leading, coaching, and inspiring others, while thriving in fast‑paced, ambiguous, and highly collaborative environments where you can think on your feet, show a growth mindset, and embrace learning through experience.

Vous apportez de solides compétences en résolution de problèmes, en analyse, en négociation et en relations interpersonnelles (à la fois écrites et orales), et vous vous sentez complètement à l'aise de voyager à l'international en fonction des besoins spécifiques du programme.

Chez Roche, nous visons haut pour fournir des solutions de santé qui changent la vie. Si vous êtes prêt à avoir un impact significatif sur les patients et les systèmes de santé dans le monde entier, c'est l'endroit qu'il vous faut.

Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.

Construisons ensemble un avenir plus sain.