Medical Director, Product Development, Cardiovascular Metabolic

Genentech; Plymouth; On-site; USD 209,000 - 389,000; Full time

Job summary

This innovative firm is seeking a Medical Director to lead clinical development strategies in the metabolic and diabetes space. You will play a pivotal role in designing and executing clinical studies, collaborating with multidisciplinary teams, and ensuring regulatory compliance. With a focus on meaningful patient improvement, this position offers the chance to impact lives through scientific advancement. If you possess a strong background in clinical research, exceptional communication skills, and a passion for drug development, this is an exciting opportunity to join a leader in the biotech industry and contribute to groundbreaking therapies.

Qualifications

• 2+ years of clinical/scientific research experience in metabolic/diabetes.
• Strong skills in data analysis and scientific writing.

Responsibilities

• Support the development and implementation of Clinical Development Plans.
• Act as a medical monitor for assigned studies and collaborate with stakeholders.

Skills

Clinical Trial Experience

Data Analysis

Scientific Writing

Communication Skills

Interpersonal Skills

Education

MD/MBBS

Job description

The Position

We advance science so that we all have more time with the people we love.

The Opportunity

Roche’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 Medical Director participates in development of the Clinical Development (CD) strategy and plan and is responsible for effective and efficient execution for the assigned molecule(s)/indication(s).

• You will support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s)/indication(s); gathering and analyzing data and information necessary to create the CD plan; you will participate in the design, development and execution of clinical studies.
• You will act as a medical monitor for assigned studies.
• You will collaborate with a variety of internal/external partners & stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc.
• You may participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input & guidance; including reviewing and providing late stage input to Phase I & II protocols.
• You have a demonstrated understanding of Phase II - III drug development.
• You will take an active role with other Clinical Science Team (CST) members, regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation; you will provide clinical science information and input for regulatory submissions and other regulatory processes.
• You will help support the strategic and operational alignment of the CD plan with the relevant CD strategy, Asset team priorities and goals; you will work with other CST members and relevant sub-teams to develop CD plan components (e.g., analytics/data strategy, KOL development, publications strategy, etc.)

Who You Are:

(Required)

• You have an MD/MBBS; board-certified (or its equivalent) training in endocrinology and/or the metabolic/diabetes space.
• You have 2+ years of post-grad relevant clinical/scientific research and/or clinical trial experience within the metabolic/diabetes space.
• You have demonstrated 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).
• You have strong communication skills in both long-form scientific presentation and short-form communication of complex scientific topics.

Preferred:

• You have knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process.
• You have demonstrated experience working with various clinical trial designs, (e.g. accelerated approval, pivotal, breakthrough etc).
• You have 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 such.
• You have strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills; has built and cultivated important relationships both inside an organization and externally. Has proven 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.

This position is based onsite in South San Francisco, CA (USA); Boston, MA (USA); Welwyn (UK) or Basel (CH).

Relocation benefits are not being offered for this position.

The review of applications will commence after January 5, 2025. Applicants selected for further consideration will be notified thereafter.

The expected salary range for this position based on the primary location of South San Francisco, CA is $209,200 - $388,600. 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.

Benefits

Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.