Boston Scientific Gruppe
About the Role
The Senior Medical Writer will be responsible for creating and supporting timely communications to support the dissemination of clinical evidence related to Interventional Cardiology Therapies (ICTx). The Senior Medical Writer will develop regulatory and scientific content including abstracts, presentations, manuscripts, and other clinical documents. The role collaborates with cross‑functional teams to support study‑specific regulatory documents, assess clinical data gaps and opportunities, and contribute to publication planning, strategy, and education activities. This position also serves as a clinical content resource for internal and external stakeholders.
Location US-MN-Maple Grove
Work Mode This is a hybrid position (in office minimum three days per week) based out of the Marlborough MA or Arbor Lakes, MN office location
Your Responsibilities
Responsible for the development, in collaboration with the clinical trial team, of study‑specific documents such as clinical protocol, clinical study reports and summaries, and clinical content that support the regulatory needs of a project.
Reviews statistical output from BSC clinical trials and registries and determines appropriate evaluation, interpretation, and presentation of data.
Responsible for the development, dissemination, and amplification of scientific clinical content in a variety of communication vehicles to ensure appropriate evaluation and presentation of data, interpretation, and alliance with business objectives.
Writes manuscripts, as well as abstracts, slide presentations, and poster presentations for scientific meetings within and outside the U.S. in support of ICTx studies.
Partners with internal and external authors (physicians/trial investigators) on manuscripts, conference abstracts, slide presentations and posters.
Identifies gaps and opportunities for compelling evidence for relevant BSC products and therapies. Works with clinical and other functions (HEMA, R&D, marketing, etc) to identify solutions to the evidence gaps identified.
Helps to organize and chair BSC study publication plan teams. Partners with investigators and internal BSC personnel to solicit feedback and develop clinical study‑related publication plans. Serve as an advisor and expert for physicians needing to access relevant clinical content.
Collaborates and provides input into clinical evidence strategy related to relevant BSC therapies.
Interacts with marketing and other groups such as Scientific Communications to ensure that clinical data is represented accurately and correctly in any published literature, slide sets, and other materials prepared by these groups.
Remains current with medical and scientific developments and publications on current/pipeline and competitor products, as well as maintaining a solid knowledge base of current data in relevant fields.
Attends scientific conferences and programs in relevant therapeutic areas to maintain current knowledge.
Required Qualifications
Minimum of 5 years of experience in clinical, research, marketing, medical affairs or product development
Proven knowledge of clinical issues associated with cardiology (structural heart, coronary therapies, and/or interventional heart failure) gained through direct or comparable relevant experience in a therapeutic area, scientific, or clinical setting
Willingness to travel up to 10% travel domestic and international
Preferred Qualifications
Solid understanding of scientific or clinical research and the scientific method, including interpretation of statistical results of clinical studies
Demonstrated scientific/medical writing acumen (e.g., manuscripts, research grants, etc.)
Ability to prepare and deliver scientific presentations, understanding of the structure and content of scientific presentations, ability to tailor presentation format and content to specific needs of topic and/or audience
Knowledge of clinical research, device/drug development processes, regulatory requirements, and good clinical practices
Compensation Minimum Salary: $86600
Maximum Salary: $164500
Nearest Major Market Nearest Major Market:
Boston Job Segment:
Clinical Research, Medical Research, Compliance, Law, Medical, Healthcare, Legal
#J-18808-Ljbffr
Location US-MN-Maple Grove
Work Mode This is a hybrid position (in office minimum three days per week) based out of the Marlborough MA or Arbor Lakes, MN office location
Your Responsibilities
Responsible for the development, in collaboration with the clinical trial team, of study‑specific documents such as clinical protocol, clinical study reports and summaries, and clinical content that support the regulatory needs of a project.
Reviews statistical output from BSC clinical trials and registries and determines appropriate evaluation, interpretation, and presentation of data.
Responsible for the development, dissemination, and amplification of scientific clinical content in a variety of communication vehicles to ensure appropriate evaluation and presentation of data, interpretation, and alliance with business objectives.
Writes manuscripts, as well as abstracts, slide presentations, and poster presentations for scientific meetings within and outside the U.S. in support of ICTx studies.
Partners with internal and external authors (physicians/trial investigators) on manuscripts, conference abstracts, slide presentations and posters.
Identifies gaps and opportunities for compelling evidence for relevant BSC products and therapies. Works with clinical and other functions (HEMA, R&D, marketing, etc) to identify solutions to the evidence gaps identified.
Helps to organize and chair BSC study publication plan teams. Partners with investigators and internal BSC personnel to solicit feedback and develop clinical study‑related publication plans. Serve as an advisor and expert for physicians needing to access relevant clinical content.
Collaborates and provides input into clinical evidence strategy related to relevant BSC therapies.
Interacts with marketing and other groups such as Scientific Communications to ensure that clinical data is represented accurately and correctly in any published literature, slide sets, and other materials prepared by these groups.
Remains current with medical and scientific developments and publications on current/pipeline and competitor products, as well as maintaining a solid knowledge base of current data in relevant fields.
Attends scientific conferences and programs in relevant therapeutic areas to maintain current knowledge.
Required Qualifications
Minimum of 5 years of experience in clinical, research, marketing, medical affairs or product development
Proven knowledge of clinical issues associated with cardiology (structural heart, coronary therapies, and/or interventional heart failure) gained through direct or comparable relevant experience in a therapeutic area, scientific, or clinical setting
Willingness to travel up to 10% travel domestic and international
Preferred Qualifications
Solid understanding of scientific or clinical research and the scientific method, including interpretation of statistical results of clinical studies
Demonstrated scientific/medical writing acumen (e.g., manuscripts, research grants, etc.)
Ability to prepare and deliver scientific presentations, understanding of the structure and content of scientific presentations, ability to tailor presentation format and content to specific needs of topic and/or audience
Knowledge of clinical research, device/drug development processes, regulatory requirements, and good clinical practices
Compensation Minimum Salary: $86600
Maximum Salary: $164500
Nearest Major Market Nearest Major Market:
Boston Job Segment:
Clinical Research, Medical Research, Compliance, Law, Medical, Healthcare, Legal
#J-18808-Ljbffr