Medical Director / Medical Science Director

Bayside Solutions is seeking a Medical Director / Medical Science Director to be part of our client's team in South San Francisco, CA. This is an opportunity to work with a biotechnology company that is determined to use cutting-edge science to identify and develop treatment to patients suffering from serious and life-threatening diseases.

Medical Director / Medical Science Director

Contract Length: 1 year

Location: South San Francisco, CA

**The company has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services are required to comply with this requirement. **

Summary of Responsibilities:

Senior/Principal Medical Director/Medical Science Director USMA OMNI Neuroscience - Alzheimer's Disease

Plays a key role in the execution of the evidence generation plan and related deliverables with a sense of urgency.

Represents the AD/gantenerumab USMA team and collaborates with internal partners (eg, AD Squad, E4A, Product Development Neuroscience, Gantenerumab Life Cycle Team, AD iSquad) in the assigned projects/studies.

Represents the AD/gantenerumab USMA team and collaborates with a variety of external partners and stakeholders, such as therapeutic area experts (TAEs), clinicians, scientists and investigators.

Collaborates with the AD/gantenerumab data communication and education team to coordinate data dissemination.

Develops and delivers compelling presentations, both internally and externally, to convey the strategic alignment and medical impact of assigned studies/projects. Includes presenting at advisory boards and other relevant external forums.

Track record on identifying innovative ways generate evidence from data gap identification to study execution (eg, decrease patient and care partner burden in trial participation, use of digital/remove technologies).

Summary of Qualifications:

• M.D., PhD, or PharmD
• 6 or more years pharma/biotech industry experience
• 4 or more years of experience with evidence generation.
• Experience or relevant knowledge of pre-approval drug development trials and/or post-marketing medical evidence generation, including expertise in controlled and observational study designs, data analysis, and clinical/health economic interpretations
• Ability to translate strategies into an actionable evidence generation plan to address needs of the complex and extensive AD customer segments, from patients and caregiver to healthcare professionals and payers.
• Understanding of the US health care environment including the payer landscape, evidence-based medicine tools and practices, and health technology assessments
• Ability to navigate complex and challenging situations and flex and thrive in an ambiguous environment.
• Familiar with competitive activity in the AD field.
• The position may require up to an additional 20% time traveling.