At Roche, over 90,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. Roche is an equal opportunity employer and rigorously prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, gender orientation, gender identity/expression, national origin/ancestry, mental/physical disability, Medical condition, marital status, veteran status, or any other characteristic protected by law.
We come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.
We are seeking a Clinical Scientist with drug development and clinical trial experience to contribute to the late stage clinical development of treatments for neuro-immunological indications. These programs may include Phase II and post-proof of concept trials including Phase III and Phase IIIb trials; close collaboration with other development teams is required.
The Clinical Scientist will work with other Clinical Scientists to collaborate with, and assist Medical Directors in all areas of project and study planning, evaluation, documentation, including annual report development, protocol development, medical monitoring for patients in the program and ongoing clinical data review. The Clinical Scientist will be a member of cross-functional teams which may include Clinical Science Team, Study Management Team, and Filing Team.
Possible tasks include:
- Provide scientific and clinical science input on clinical development plans.
- Stay up-to-date on internal and external developments and continue to develop scientific and clinical knowledge relevant to neuro-immunological disorders,
- Provide clinical science support for ongoing and future clinical development programs
- Ongoing data review of clinical trials
- Collaborate with a variety of internal and external organizations and partners, such as clinical investigators, other groups in Product Development, research, business development, legal, etc.
- Provide scientific input into internal and external study documents and presentations. Specifically, contribute to clinical science sections of Health Authority meeting packages and assists in the development and review of clinical documentation required for regulatory filings and other regulatory documentation
- Ensure Good Clinical Practice (GCP) and Standard Operating Procedures are followed
Who you are:
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
- You have an advanced degree, preferably a PhD in neuroscience or related discipline. Several years’ experience in drug development within the bio-pharmaceutical industry and/or prior experience in running trials in the Neuroscience space is expected.
- You have experience working in multi-functional development teams.
- You are able to evaluate, interpret/synthesise scientific data, and to verbally present and critically discuss clinical trial data in internal and external meetings
- You have excellent verbal and written interpersonal skills in English
Are you ready to apply? We want someone who thinks beyond the job offered - someone who knows that this position can be a rare springboard to many other opportunities at Roche.
Roche is an equal opportunity employer.Research & Development, Research & Development > Clinical Development