What are the responsibilities and job description for the Sr Manager Scientific Communications position at BioSpace?
Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Worldwide Research And Development
From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
REMOTE Responsibilities may include, but are not limited to: Publication Strategy and Planning Collaborate with cross-functional team during publication strategy meetings to develop and ensure timely execution of the scientific communication plan for BioMarin’s Skeletal Dysplasia program Develop expert knowledge of product- and disease-specific literature and oversee literature and gap analyses to support scientific message development and publication strategy Organize and implement expert meetings necessary for publication strategy development; collaborate with MDs to develop agenda and content, manage vendors, and attend and present as needed Support scientific congress activities including development of content for symposia and medical booth materials Facilitate the external/independent development of treatment and management guidelines Publication Content Creation Research, draft, and edit scientific and medical manuscripts, abstracts, posters, and presentations Critically analyze complex information and collaborate with clinical/medical and statistical teams on data analysis, interpretation, and presentation Manage agency and/or contract medical writers and/or graphic designers, as needed Ensure all scientific communications outputs meet the highest standards of medical/scientific integrity Ensure that key data, statements, and conclusions included in publications and other deliverables are consistent with scientific messaging, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data Identify and propose resolutions for data quality issues in collaboration with MDs and statistical team during data interrogation Ensure activities adhere to authorship and publication guidelines as stipulated by ICMJE and GPP 2022 Assist with maintenance and reconciliation activities within publication development database Other Respond to internal and external questions about any scientific communications for the product area Ensure that important information is shared with managers, peers, and business partners in a timely manner to enable effective decision-making and/or execution of strategic priorities Participate in cross-functional team meetings to share scientific communication planning status and issues and maintain awareness of overall scientific communication plan Provide support for management of the Scientific Communications Skeletal Dysplasia budget Skills Excellent written and verbal communication skills Ability to interpret, analyze and communicate complex scientific data Understanding of statistical and clinical research concepts Understanding of biotech/pharmaceutical clinical and regulatory processes Strong project management skills and ability to prioritize tasks and work on multiple projects Demonstrated ability to work effectively in cross-functional teams Extensive experience with graphic design software (Adobe Creative Suite), medical content management systems (iEnvision, Veeva), and biomedical reference databases (e.g., PubMed) preferred Strong data visualization and graphic presentation skills preferred EducationBachelor’s degree in life or health sciences; advanced degree preferred but will consider extensive work experience in lieu of advanced degree 5 years work experience
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Worldwide Research And Development
From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
REMOTE Responsibilities may include, but are not limited to: Publication Strategy and Planning Collaborate with cross-functional team during publication strategy meetings to develop and ensure timely execution of the scientific communication plan for BioMarin’s Skeletal Dysplasia program Develop expert knowledge of product- and disease-specific literature and oversee literature and gap analyses to support scientific message development and publication strategy Organize and implement expert meetings necessary for publication strategy development; collaborate with MDs to develop agenda and content, manage vendors, and attend and present as needed Support scientific congress activities including development of content for symposia and medical booth materials Facilitate the external/independent development of treatment and management guidelines Publication Content Creation Research, draft, and edit scientific and medical manuscripts, abstracts, posters, and presentations Critically analyze complex information and collaborate with clinical/medical and statistical teams on data analysis, interpretation, and presentation Manage agency and/or contract medical writers and/or graphic designers, as needed Ensure all scientific communications outputs meet the highest standards of medical/scientific integrity Ensure that key data, statements, and conclusions included in publications and other deliverables are consistent with scientific messaging, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data Identify and propose resolutions for data quality issues in collaboration with MDs and statistical team during data interrogation Ensure activities adhere to authorship and publication guidelines as stipulated by ICMJE and GPP 2022 Assist with maintenance and reconciliation activities within publication development database Other Respond to internal and external questions about any scientific communications for the product area Ensure that important information is shared with managers, peers, and business partners in a timely manner to enable effective decision-making and/or execution of strategic priorities Participate in cross-functional team meetings to share scientific communication planning status and issues and maintain awareness of overall scientific communication plan Provide support for management of the Scientific Communications Skeletal Dysplasia budget Skills Excellent written and verbal communication skills Ability to interpret, analyze and communicate complex scientific data Understanding of statistical and clinical research concepts Understanding of biotech/pharmaceutical clinical and regulatory processes Strong project management skills and ability to prioritize tasks and work on multiple projects Demonstrated ability to work effectively in cross-functional teams Extensive experience with graphic design software (Adobe Creative Suite), medical content management systems (iEnvision, Veeva), and biomedical reference databases (e.g., PubMed) preferred Strong data visualization and graphic presentation skills preferred EducationBachelor’s degree in life or health sciences; advanced degree preferred but will consider extensive work experience in lieu of advanced degree 5 years work experience
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
