Medical Science Liaison

Proclinical is currently recruiting for a new job opportunity at a biopharmaceutical company focused on developing cancer treatments. They are currently recruiting for an experienced Medical Science Liaison to join their expanding team in Germany. This is an exciting time to join this company who operate across the United States, Europe and other international markets and have an extensive pipeline of products under development.

This Medical Science Liaison job contributes to the development of medical strategy and provides medical and scientific expertise into Brand Strategies for all Clovis Oncology products within UKINORD cluster. This role works to execute the medical component of the Brand Strategies working cross functionally to ensure optimal delivery.

Job Responsibilities:

• Contribute to the development of the Medical component of the Brand Strategy, and develop a tactical Medical Plan for each assigned product, in support of the Brand Plans.
• Support the marketing and market access strategy for all Clovis Oncology products by being a key member on cross functional teams.
• Support the management of Investigator Initiated Trials (IITs) and phase IV clinical studies in the UKINORD.
• Review promotional materials and Regulatory documents for medical accuracy and compliance with applicable guidelines and regulations.
• Work with regional medical information to ensure cluster consistency and compliance for medical information standard letter and responses
• Management of cluster level Grants & Sponsorships ensuring proper documentation, contracts and payment.
• Work with MSL to develop the KOL and Stakeholder engagement plans in accordance with the overall strategic brand/medical plans.
• Manage local publications related to Clovis Oncology products and disease area of focus.
• Liaison with Clovis Oncology Clinical Operations team to ensure optimal cluster KOL involvement and support of Clovis Oncology trial programme.
• Provide or collaborate with the UKINORD MSL team to develop scientific tools required for them to successfully perform their job (e.g. scientific platform content, presentation of new data, etc.).
• Contribute to the development, attend and present at appropriate meetings (advisory board meetings, investigator meetings, KOL meetings, etc
• Develop and maintain a good working relationship and interact directly with Global Medical Affairs, Clinical Operations, other Clovis Oncology clusters to understand global strategy and share best practices.
• Provide cross-functional therapeutic and product expertise to internal customers.
• Develop and maintain up-to-date knowledge of the therapy areas by reviewing the literature, discussions with Key Opinion Leaders and key stakeholders, participating in cross functional interactions, attending scientific congresses, etc.
• Provide therapeutic area and product training as needed.
• Support the development/revision and implementation of UKINORD cluster Standard Operating Procedures, local Working Instruction and process guidance as required.
• Ensure all Medical activities are compliant with appropriate Clovis Oncology Policies, SOP's, Good Clinical Practice (GCP) and ICH guidelines.
• Participate in personal development and training sessions.

Skills and Requirements:

• Understanding of pharmaceutical commercial, medical and scientific needs on a local and European basis.
• Intimately familiar with applicable rules and regulations and actions of EU regulatory bodies within the assigned Country/Region.
• Solid peer relationships with and exposure to external scientific and clinical experts and Key Opinion Leaders; demonstrated ability to proactively engage internal and external leaders and serve as a medical expert for the Oncology disease area in the Country/Region.
• Recognized expertise in clinical and/or research experience (including publications) in therapy area is desired; specialty training and/or clinical experience in oncology is highly preferred.
• Proven ability to translate and appropriately align commercial and scientific goals and objectives and to interact productively with both scientific and commercial colleagues.
• Highest ethical standards in corporate medical governance.
• Successful track record of initiating and leading cross-business/cross-functional planning, collaborating and solution building.
• Strong interpersonal skills to allow for successful interaction with peers across the organization to achieve corporate goals.
• Excellent written and oral communication skills.
• English proficiency a must; fluency in the language of the Region is essential.
• GMC registered physician or UK GPC registered pharmacist.
• Relevant medical affairs or related industry experience in Oncology with demonstrable experience and contribution to commercial, medical affairs.
• PMCPA final signatory status preferred.

To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Divya Mistry on +44 203 814 1315 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
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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