Clinical Development Medical Director - Immuno-Oncology job in Lausanne, Switzerland

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First Name*

Last Name*

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Phone Number*

Country*

Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Project/Study Manager (CSM/CPM)

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

Proclinical is in search of a Clinical Development Medical Director with a speciality in oncology, in Switzerland. This role is responsible for implementing clinical drugs for oncology products from Phase I through to Phase III. If you're interested in driving healthcare forward this might be the role for you.

Job Responsibilities

Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilence and clinical operations
Interacts with global regulatory bodies including the FDA and EMA to accomplish tasks related to oncology product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and New Drug Applications (NDAs)
Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, investigator brochure, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans
Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies
Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development
Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development
Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies
Works in partnership with medical affairs for successful launch of future anti¬neoplastic agents
Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents
Provides guidance for successful implementation and accomplishment of investigator initiated trials related to product development and life cycle management
Act within compliance and legal requirements as well as within company guidelines

Skills and Requirements

M.D. or D.O. degree with a minimum of 3 - 5 years of experience (6+ years - senior) in oncology drug development in a biotechnology or pharmaceutical company
Board certified or eligible in Oncology preferred
Experience with early phase oncology trials
Ability to multi-task and work in a face paced environment

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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