v Medical Director | Work In Cannabis

 

Medical Director


Full TIme - Cleveland, OH
POSTED: 04.03.2017

Medical Director 

The Role

This individual will be responsible for ensuring the global medical integrity of the cannabinoid development program, and shaping and developing the global medical affairs strategy to support one or more products that are currently in clinical development.

The role can be the best thought of as a ‘hybrid’ one working across R&D and Medical Affairs from both an operational and geographical perspective, with the focus evolving over time.

Key Responsibilities

Developing constructive working relationships with external stakeholders including key opinion leaders, principal investigators, patient advocacy groups, and may include regulatory interactions. Internally, key working relationships will be global marketing, US medical affairs, clinical research, and regulatory affairs

Essential skills:

Broad skill set in Medical Affairs, Clinical development, Drug safety, and regulatory affairs

Strong customer orientation, science-based and marketing minded negotiation skills

Operational excellence, Management skills, planning, prioritization, decision making, objective setting, meeting management and plan execution

Medical Education (MD); Clinical Development and Medical Affairs.

Experience within pharmaceutical or biotech,

Knowledge of Pharmaceutical product development, product lifecycle and commercialisation process with advanced understanding of other functions including Clinical Operations, Commercial, regulatory, safety, medical and market access.

Statistical analysis

Solid understanding of research study design and relevant development guidelines

Medical affairs experience across one or more EU country

Neurology specialist experience

Strong business acumen

Desirable skills:

Epilepsy experience

ABPI code of practice certified

Pharmaceutical affiliate and global experience

Knowledge of pharmaceutical regulations and pharmacoeconomics

Working in cross-functional teams in a matrix environment

Finance/budgeting and resource management experience

Leadership experience

ABOUT THE JOB
DETAILS

This individual will be responsible for ensuring the global medical integrity of the cannabinoid development program, and shaping and developing the global medical affairs strategy to support one or more GW products that are currently in clinical development and which GW intends to market in the US and ROW. As such the role can perhaps be best thought of as a ‘hybrid’ one working across R&D and Medical Affairs from both an operational and geographical perspective, with the focus evolving over time.

REQUIRED SKILLS

Broad skill set in Medical Affairs, clinical development, Drug safety and regulatory affairs Strong customer orientation, science based and marketing minded, negotiation skills Operational excellence, Management skills, planning, prioritization, decision making, objective setting, meeting management and plan execution Medical Education (MD); clinical development and medical affairs. Experience within pharmaceutical or biotech, Knowledge of Pharmaceutical product development, product lifecycle and commercialisation process with advanced understanding of other functions including Clinical Operations, Commercial, regulatory, safety, medical and market access. Statistical analysis Solid understanding of research study design and relevant development guidelines Medical affairs experience across one or more EU country Neurology specialist experience Strong business acumen

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