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Mansueto Ventures is home to two of the most iconic and vibrant brands in business publishing: Inc. and Fast Company. Every day, the content, awards, and events produced help entrepreneurs and innovators succeed by providing useful insights, sparking essential conversations, and offering much-needed inspiration.

Inc. is the voice of the American entrepreneur, inspiring and documenting the risk-takers and ultra-driven go-getters who represent the most dynamic force in the American economy.
Fast Company is the world’s leading business media brand, focusing on innovation in technology, leadership, and design to inspire readers to shape the future of business.

","New York, NY","coloredLogo","logoAttachment","thumbnail","thumbnailAttachment","hexCode","#080D0C","headline","Publisher of Inc. and Fast Company, empowering innovators and entrepreneurs.","/companies/mansueto-ventures-careers","hasJobSubmission","isSavedJob","similarJobs",[511,519,526,536,544],{"_429":428,"_434":512,"_452":453,"_444":445,"_243":438,"_441":438,"_427":428,"_111":513,"_431":432,"_433":194,"_454":453,"_442":443,"_425":514,"_455":456,"_430":115,"_476":515,"_460":516,"_478":517,"_480":443,"_482":483,"_484":485,"_486":518},["D",1771200000000],"Lead Medical Director, Product Development, Gastroenterology, & Hepatology",["B","2619539496"],"3 days ago","/jobs/2619539496-lead-medical-director-product-development-gastroenterology-hepatology","Lead Medical Director, Product Development, Gastroenterology, & H...","/jobs?keyword=Lead+Medical+Director%2C+Product+Development%2C+Gastroenterology%2C+%26+H...",{"_429":428,"_434":520,"_452":453,"_444":445,"_243":438,"_441":438,"_427":428,"_111":521,"_431":432,"_433":194,"_454":453,"_442":443,"_425":522,"_455":456,"_430":115,"_476":523,"_460":524,"_478":521,"_480":443,"_482":483,"_484":485,"_486":525},["D",1771372800000],"Medical (Science) Director - Rare Blood Disorders/Hematology",["B","2623869388"],"1 days ago","/jobs/2623869388-medical-science-director-rare-blood-disorders-hematology","/jobs?keyword=Medical+%28Science%29+Director+-+Rare+Blood+Disorders%2FHematology",{"_429":428,"_434":527,"_452":453,"_444":445,"_243":528,"_441":529,"_427":428,"_111":530,"_431":194,"_433":194,"_454":453,"_442":531,"_425":532,"_455":456,"_430":115,"_476":523,"_460":533,"_478":530,"_480":531,"_482":483,"_484":534,"_486":535},["D",1771408800000],"The Position\nRoche’s Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients.

The Senior Medical Director leads development of the Clinical Development (CD) strategy and plan and is responsible for ensuring effective and efficient execution for the assigned molecule(s)/indication(s). Senior Medical Directors are expected to perform their responsibilities independently, and effectively lead multiple projects. Our late stage, clinical development organization is structured by therapeutic area and is responsible for developing and executing the late development clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients.

You will lead, delegate and be responsible for the development and implementation of the CD strategy and/or plan for assigned molecule(s)/indication(s); you will represent CD for the assigned molecule(s)/indication(s) to other internal Roche groups; you will be responsible for ensuring cross-functional integration, coordination and alignment to enable effective and efficient CD plan execution

You will collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, business development, commercial operations, legal, etc.

You may participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance; includes reviewing and providing late stage input into Phase I and II protocols

You will lead health authority (HA) interactions, including the development of briefing packages by providing clinical science information and input; you will take a lead role with other CST members, regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation; providing clinical science information and input for regulatory submissions and other regulatory processes. Includes developing label and packaging language, etc.

You will be accountable for training new CST members

This role is based in Boston, MA (USA).\nRelocation benefits are being offered for this role.

Who You Are:\n(Required)

You are a Board Certified/Board Eligible (or its equivalent) MD (MBBS), MD(MBBS)/PhD trained Gastroenterologist/Hepatologist, Endocrinologist or Cardiologist

You have 6+ years of pharma/biotech R&D experience and/or is recognized as an expert in your field; you can effectively contribute to pipeline strategy and lead cross-functional teams.

You have late stage experience within the CVRM space and have worked with various health authorities.

You have demonstrated the ability to work with pharma partnering on relevant acquisitions, joint ventures or other strategic partnerships

You have significant experience designing and conducting clinical trials (i.e. one or more trials)

You have demonstrated experience in late stage development; you have the proven ability to use sophisticated analytical thought, identify innovative approaches and act a mentor

You have demonstrated the ability to foster and promote a highly productive and inclusive team-based culture in fast-paced clinical and/or research settings

You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance, and demonstrated experience in scientific writing (e.g. manuscripts, grants, scientific protocols, health authority documents)

You have outstanding communication skills in both long-form scientific presentation and short-form communication of complex scientific topics

You have demonstrated the ability to collaborate with relevant team members to measure and monitor study progress against objectives and plans, including any variances, and proactively communicate any issues, challenges and potential strategies to resolve

You are experienced working with various clinical trial designs

Preferred:

You have leadership experience.

You have strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills: have built and cultivated important relationships both inside and outside of the organization and externally; have proven abilities to influence internal partners and stakeholders, thought leaders, national advocacy organizations, national standard-setting bodies, and other relevant external parties.

You have the proven ability to use sophisticated analytical thought, identify innovative approaches and act as a mentor.

You have demonstrated the abilities to influence internal partners and stakeholders, thought leaders, national advocacy organizations, national standard-setting bodies, and other relevant external parties. Seamlessly collaborates with colleagues/other parts of the organization.

The expected salary range for this position based in Boston, MA (USA) is $231,500 - $430,250. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position qualifies for the benefits detailed at the link provided below:

Benefits

#PDC2026

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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Head Of Us Lab For Aurora

We're passionate about delivering on Our Promise to improve the lives of patients and create healthier communities for all. We foster a culture of inclusivity, integrity, and creativity while boldly pursuing answers to the world's most complex health challenges and transforming society.

Genentech is seeking a dynamic and strategic leader to serve as the Head of the US Lab for AURORA. This is a critical leadership role responsible for the operational excellence and strategic growth of our in-house content engine. As the Head of the US Lab, you will be pivotal in shaping the future of content creation at Genentech, ensuring that the AURORA Lab becomes a vital partner to the Marketing and Digital, Data, and Analytics (DDA) organizations.

You will lead the US-based operations of the AURORA Lab, with a mandate to not only deliver high-quality, compliant marketing content with industry-leading speed and efficiency but also to expand the Lab's footprint and influence across the wider Genentech organization. This role requires a leader who can build strong partnerships, drive innovation, and foster a culture of continuous improvement. You will work in close partnership with the Director, Marketing Creative Execution Lead, to ensure seamless integration between creative strategy and operational execution.

Key Responsibilities

Define and execute the strategic vision for the US Content Lab, aligning its capabilities with the evolving needs of the Marketing and DDA organizations.
Act as the primary relationship owner for the AURORA Lab within the US, cultivating and growing strategic partnerships with key stakeholders across the Genentech organization.
Champion the AURORA Lab's value proposition, proactively identifying opportunities to expand its services and deepen its integration with brand marketing and other functional areas.
Develop and manage the US Lab's budget, resource planning, and performance metrics, reporting on progress to key stakeholders.

Lead the strategic evolution of the AURORA Lab's operating model, overseeing the transition from the current state to a future state designed for high-volume production.
Lead the day-to-day operations of the US Lab, ensuring the efficient and effective delivery of all content projects.
Serve as the primary escalation point for all operational issues, providing clear direction and timely resolution.
Lead, mentor, and develop a high-performing team of content professionals, fostering a collaborative and inclusive work environment.
Implement and manage a robust system for daily and weekly reporting of ticket volumes, throughput, and other key performance indicators to ensure transparency and drive continuous improvement.

Work in close partnership with the Director, Marketing Creative Execution Lead, to align on a shared vision, roadmap, and implementation plan for content excellence.
Collaborate with brand marketing to identify opportunities to optimize impact and improve efficiency across creative execution.
Ensure seamless integration with external partners and vendors, managing operational touchpoints and workflows to maximize efficiency and quality.

Who You Are

You hold a Bachelor's degree; MBA or other related graduate-level degree and 12+ years of marketing experience in relevant industries.
You have working experience in the managed care, pharmaceutical or biotech industry/pharmaceutical or biotech customer engagement teams.
You have experience running content operations at scale for large pharma and/or agency experience and applied Lean six sigma or equivalent agile process at scale.
You have experience in creating marketing strategies, plans, and tactics that have strengthened market positioning and financial results.
Prior experience in managing relationships with external vendors and partners required, direct agency of record experience preferred.
You have extensive experience in content creation workflows across digital channels.
You have experience facilitating cross-functional engagement, relationship building and collaboration.
You have strong analytical skills, with the ability to use data to drive decision-making and continuous improvement.
You are familiar with regulatory requirements for digital content in the pharmaceutical industry.
You possess strong organizational, interpersonal, leadership and communication skills with proven attention to detail.
You have a proven track record of executing large-scale, highly strategic initiatives and have the ability to thrive in an ambiguous environment.
You have a strong understanding of digital marketing trends, technologies, and best practices.

Location: This position is based in South San Francisco, CA. Relocation assistance is not available at this time.

The expected salary range for this position, based on the primary location of CA, is $187,100 - $347,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This position also qualifies for the benefits detailed at the link provided below.

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form. Accommodations for Applicants.

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Head Of Us Lab For Aurora

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