Genentech discovers, develops, manufactures and commercializes treatments for patients with serious and life-threatening medical conditions. Backed by North Carolina Biotechnology Center.
About the role
This role is located at Roche’s Genentech campus in South San Francisco, California. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Good influencing and negotiation skills. Demonstrates ability to lead diverse teams and influence stakeholders of varying organizational levels without direct authority
- Good time management and organizational skills. Consistently meets deadlines without compromise to quality of work
- Strong attention-to-detail, as demonstrated through consistent quality of work
- Demonstrates process-orientation. Thinks through required steps and sequencing to ensure quality work output
- Demonstrates ability to identify appropriate resources
- Bachelors Degree (life sciences, law, public policy, marketing, business, education, or related discipline preferred)
More about this role
Commercial Regulatory Affairs (CORA) is part of the Global Product and Access Legal (GPAL) organization that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for Roche’s global Pharma Division. The CORA Group reports into the Head of GPAL in the Global Legal Pharma Department.
Associate Program Directors of Commercial Medical Legal Regulatory Review Committees (CMLRs) provide regulatory support for assigned products or cross-portfolio activities and can lead cross-functional CMLRs with oversight from CORA Program Directors and their managers. They are experienced individual contributors expected to perform responsibilities with increased independence.
- Lead CMLRs and effectively collaborate with cross-functional groups and advertising agencies.
- Provide regulatory support to assigned products, business areas, and projects, providing sound regulatory guidance.
- Manage other departmental projects and deliverables, proactively identifying and addressing compliance issues.
- Effectively integrate regulatory...
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