Associate Director, Scientific & Medical Affairs (Contract)
Redwood City, California, United States · Remote OK
$65/hr–$110/hr
Senior$815M raised
Adverum Biotechnologies, wholly owned subsidiary of Eli Lilly and Company, is looking for an Associate Director, Scientific & Medical Affairs (Contract) to join our team. This role will be responsible for scientific comm…
Skills: Scientific communication, Medical affairs, Clinical trial data analysis, Publication planning, Medical writing
Redwood City, California, United States · Remote OK
$75/hr–$130/hr
Senior+$815M raised
Adverum Biotechnologies, wholly owned subsidiary of Eli Lilly and Company, is looking for a Director, HEOR (Contract) to join our team. The Director, HEOR leads the development and execution of evidence generation strate…
Skills: HEOR strategy, Evidence generation, Ophthalmology, Retina, Clinical development
Adverum Biotechnologies, Inc., a wholly owned subsidiary of Eli Lilly and Company is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular disea…
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$65/hr–$110/hr
Contract
postgraduate degree
Paid sick leave
Posted 7d ago
~40 hrs/week
Remote in Redwood City, California, United States
Responsibilities
The Associate Director will lead scientific communication and medical affairs activities, including the development of publication plans and clinical data interpretation. They will also serve as a scientific expert, collaborating with cross-functional teams and external stakeholders to support clinical trial and launch initiatives.
Requirements
Candidates must hold a terminal degree such as a PharmD, PhD, or MD and possess 5-7 years of industry experience. Proficiency in ophthalmology or gene therapy, along with strong publication experience and communication skills, is highly desired.
Full job description
Adverum Biotechnologies, wholly owned subsidiary of Eli Lilly and Company, is looking for an Associate Director, Scientific & Medical Affairs (Contract) to join our team. This role will be responsible for scientific communication and medical affairs activities including clinical trial, pre-launch and launch.
Note to Recruiters and Agencies
All recruiters and agency inquiries must go through the Adverum internal Talent Team. Unsolicited resumes sent to Adverum will be considered Adverum's property. Adverum’s Talent Acquisition team must expressly engage agencies for any requisition.
\nWhat you'll do:
Collaborating with the Medical affairs and clinical development in driving quality control and endorsement of: Scientific Communication Platforms, Lexicons, Disease-State Education materials, Program Slides, Data/Publication updates, Congress materials.
Serve as a key scientific lead, providing editorial, scientific and strategic expertise for assigned projects
Lead research focused data analysis and interpretation of clinical trial data (sub analysis, post hoc analysis) to leverage for future podium presentations and publications
Develop and implement strategic publication plans in collaboration with cross-functional TA teams (Medical, Real-World Evidence) including internal authors, R&D clinical leads, and study statisticians
Provide medical writing review and assistance for scientific communications (publications, medical affairs materials) as well as manage external vendors
Responsible for efficient review (and sometimes) preparation and delivery of high-quality publications, presentations, and abstracts; review all project-related content for accuracy and consistency
Serve as an extension of Field medical and attend conferences, cover scientific sessions and booth and serve as a scientific expert with external stakeholders, KOLs and healthcare professionals
Contribute to innovative communications including using interactive PDFs, infographics, podcasts, and novel digital media with agency support for internal and external collaborators
Facilitate discussions regarding dissemination of published data and contribute to the strategic scientific communications plan and platforms
Lead projects and deliver documents within process/timeline constraints
About you:
Terminal degree required (PharmD, PhD, MD, or equivalent)
Ophthalmology or gene therapy experience highly desired
Minimum of two years of publication experience is preferred + 5-7 years industry experience
Self-starter and self-motivated
Demonstrated experience effectively presenting clinical/scientific information required
Ability to learn other disease states if necessary
Excellent communication and presentation skills required
Demonstrated ability to build productive collaborations with medical experts
Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware required
Must be a strong team player and effectively interface with internal departments including Clinical Development, Clinical Operations, Translational Research, Technical Operations, Medical Affairs, the office of the Chief Medical Officer
Must be willing to travel to company meetings, and to medical congresses
Exhibits excellent time management and able to work independently
Able to thrive as part of a team and when working independently
Must be well organized, polished, proactive, detail-oriented, mature, and have a professional demeanor
\n
$65 - $110 an hour
This contract role will be managed and payrolled through one of our preferred vendors, who will be your employer of record for the duration of the assignment. The hourly range for this position is between $65.00 USD to $110.00 USD per hour. This hourly range is an estimate, and the actual hourly rate may vary based on a candidate’s qualifications, including education, length of experience, location, and market data. The vendor will provide compensation and benefit options in accordance with specific state requirements, including paid sick leave accrual.
As a team member of Adverum Biotechnologies, a wholly owned subsidiary of Eli Lilly, during your assignment, you'll work alongside our Medical Affairs team and broader cross-functional teams, and the opportunity to contribute to meaningful work within gene therapy, ophthalmology care.
We are on a global mission to establish gene therapy as a new standard of care for the leading causes of vision loss.
Industry
Biotechnology Research
Company size
51-200 employees
Founded
2012
Headquarters
Redwood City, California
LinkedIn followers
15,303
Total funding
$815M
Adverum Biotechnologies (NASDAQ: ADVM) is a clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary, intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies, designed to be delivered in physicians’ offices, to eliminate the need for frequent ocular injections to treat these diseases. Adverum is evaluating its novel gene therapy candidate, ixoberogene soroparvovec (Ixo-vec, formerly referred to as ADVM-022), as a one-time, IVT injection for patients with neovascular or wet age-related macular degeneration. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
A wholly-owned subsidiary of Eli Lilly and Company.
Offices: 100 Cardinal Way, Redwood City, California 94063, US
We are on a global mission to establish gene therapy as a new standard of care for the leading causes of vision loss.
Industry
Biotechnology Research
Company size
51-200 employees
Founded
2012
Headquarters
Redwood City, California
LinkedIn followers
15,303
Total funding
$815M
Adverum Biotechnologies (NASDAQ: ADVM) is a clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary, intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies, designed to be delivered in physicians’ offices, to eliminate the need for frequent ocular injections to treat these diseases. Adverum is evaluating its novel gene therapy candidate, ixoberogene soroparvovec (Ixo-vec, formerly referred to as ADVM-022), as a one-time, IVT injection for patients with neovascular or wet age-related macular degeneration. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
A wholly-owned subsidiary of Eli Lilly and Company.
Offices: 100 Cardinal Way, Redwood City, California 94063, US