Publicada el 15 junio
Misión del puesto
Who We Are
At Roche Diagnostics Solutions (RDS), our mission is to diagnose earlier, develop faster, and personalize treatment because every patient is unique. Our Clinical Development & Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally.
We collaborate with internal teams, external partners, and patients to provide crucial medical insights, design and execute clinical studies, and offer on‑market support. Our work spans the entire product lifecycle—from discovery to post‑launch—generating comprehensive clinical evidence that demonstrates product safety, effectiveness, and scientific validity, thereby facilitating smooth product registration, adoption, and reimbursement worldwide.
The Opportunity
- Lead global study teams with full accountability for high‑quality clinical trial deliverables, managing timelines, milestone execution, and multi‑million‑dollar clinical budgets.
- Design and execute innovative global operational study strategies in cross‑functional collaboration with Clinical Development, Regulatory Affairs, and Research & Development teams.
- Develop and validate fundamental study documentation, including clinical protocols, design validation plans, and essential investigator templates.
- Deliver robust operational oversight for diverse clinical programs, including Investigator‑Initiated Studies, Early Adopter Programs, and strategic partner collaborations.
- Manage international clinical vendor portfolios (CROs, functional consultants, medical advisors), leading selection processes and driving high‑performance execution.
- Build collaborative, high‑impact partnerships with international medical investigators, opinion leaders, and global alliance partners to integrate cutting‑edge healthcare expertise into operational designs.
Who You Are
- You bring a minimum of a Bachelor’s degree in Life Sciences, Healthcare, or a closely related field, combined with established experience in general clinical operational roles.
- You possess strong, practical expertise managing clinical study development phases (from initial planning and start‑up through conduct to active study close‑out).
- You demonstrate deep working knowledge of international clinical regulations and standards (such as ICH‑GCP, IVDD/IVDR, MDR, or FDA guidelines) to proactively maintain inspection‑readiness.
- You are an agile communicator and collaborative leader, capable of resolving complex problems, building cross‑functional consensus, and guiding project teams through fast‑paced, matrixed environments.
- You are deeply passionate about fostering an environment of belonging, working seamlessly across diverse regions, cultures, and time zones to put the needs of patients first.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.
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