Medical Director Dermatology Clinical Development

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.

The Position

Roches 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. We have an opportunity for a Medical Director with a background in dermatology to join our clinical development team for a 1 year fixed term contract.

The Opportunity

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 CDP; 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 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 be responsible to ensure strategic and operational alignment of the CDP with the relevant Asset team strategy priorities and goals; you will work with other CST members and relevant sub-teams to develop CDP components (e.g. analytics / data strategy KOL

development publications strategy etc.)

Who You Are

You have an MD board-certified training in dermatology or substantial dermatology-specific research and clinical experience and have 2 years of post-graduate relevant clinical / scientific research and / or clinical trial experience

You have knowledge of the pharma / biotech industry the multiple functions and roles involved in the drug development process.

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)

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 : You demonstrate strong communication skills in both long-form scientific presentation and short-form communication of complex scientific topics. You have the ability to build and cultivate important relationships both inside an organization and externally. You influence internal partners and stakeholders thought leaders national advocacy organizations national standard-setting bodies and other relevant external parties.

If you are a dermatologist with clinical study experience and looking to make an impact in an area of unmet need we would love to hear from you. Apply by submitting your CV and cover letter via our careers portal.

Who we are

A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.

Lets build a healthier future together.

Roche is an Equal Opportunity Employer.

Required Experience :

Director

Key Skills

EMR Systems,Post Residency Experience,Occupational Health Experience,Clinical Research,Managed Care,Primary Care Experience,Medical Management,Utilization Management,Clinical Development,Clinical Trials,Leadership Experience,Medicare

Employment Type : Full-Time

Experience : years

Vacancy : 1