BioSpace
Senior Manager, Medical Writing (Remote)
BioSpace, South Chicago Heights, Illinois, United States
Senior Manager, Medical Writing (Remote)
BioSpace – Remote
Summary Responsible for development, implementation, and maintenance of documents and/or business systems utilized for writing project support. Address and resolve issues within assigned therapeutic area(s). Interface with functional groups and writers to ensure timely completion of projects that are scientifically accurate and of high quality. Leads writing project efforts for team. Assists in selection, supervision, and project resourcing for writing team within assigned therapeutic area(s).
Responsibilities
Serves as Medical Writing Lead on more complex writing assignments implementing all activities related to the preparation and compilation of data and information into assigned writing projects.
Leads writing project efforts for team and recognizes potential scheduling and resource conflicts for projects across therapeutic area/product assignments and provides recommendations to resolve.
Assists in selection, supervision, and project resourcing for writing support within assigned therapeutic area(s).
Accountable for meeting the main objectives of clinical writing projects in therapeutic area(s) within established timelines, budgets, and with an appropriate quality level.
Provides project management for writing projects for multiple compounds and/or indications within assigned therapeutic area, ensuring accuracy and adherence to timelines and processes.
Works directly with team members to develop/implement timelines to meet desired project completion dates and coordinates activities and communication with functional areas on writing projects.
Effectively collaborates with clinicians and management utilizing cross‑functional skills/expertise and scientific knowledge.
Proficiently learns and applies therapeutic area and product knowledge to scientific projects; develops expert knowledge of regulations, requirements, policies, and guidelines for writing projects.
Maintains and leads productive cross‑functional working teams, implements systems or solutions to enhance efficiency, eliminate redundancy, reduce expenditure, and guarantee quality.
Oversees writing projects to ensure timely completion, resolves conflicts, removes barriers, and generates innovative ways to ensure teams achieve project goals.
Continually trains/be compliant with all current industry requirements as they relate to assigned writing projects.
Qualifications
Bachelor’s degree in English or Communications with relevant science expertise or Bachelor’s degree in Life Science with relevant writing expertise; Advanced degree and/or professional certification preferred.
3 years relevant industry experience required; 5 years in medical writing in healthcare industry, academia, or related area such as quality, regulatory, publications, clinical research, or product support/R&D; 4 years in experimental design and clinical/preclinical data interpretation; 2 years in a project management role.
Form, maintain, and lead productive cross‑functional working teams; track record of collaboration and leadership.
Working knowledge of applicable regulations and legislation.
Excellent business communication skills with aptitude for summarization and detail orientation.
Experience developing and delivering presentations to senior management.
Ability to understand and interpret medical data and create strategic messaging.
Knowledge of product therapeutic area preferred.
Microsoft Office and Internet navigation proficiency; working knowledge of statistical concepts; other business‑related IT proficiency.
Identify and employ rigorous logic and methods to solve problems independently; recognize potential scheduling/resource conflicts and provide solutions.
Benefits and Compensation
Comprehensive benefits package including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) for eligible employees.
Eligibility to participate in short‑term and long‑term incentive programs.
Base pay range (subject to geographic location) and potential for additional compensation.
Equal Opportunity Employer, veterans/disabled accepted.
Equal Opportunity Statement AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Marketing, Public Relations, and Writing/Editing
Industry: Internet News
#J-18808-Ljbffr
Summary Responsible for development, implementation, and maintenance of documents and/or business systems utilized for writing project support. Address and resolve issues within assigned therapeutic area(s). Interface with functional groups and writers to ensure timely completion of projects that are scientifically accurate and of high quality. Leads writing project efforts for team. Assists in selection, supervision, and project resourcing for writing team within assigned therapeutic area(s).
Responsibilities
Serves as Medical Writing Lead on more complex writing assignments implementing all activities related to the preparation and compilation of data and information into assigned writing projects.
Leads writing project efforts for team and recognizes potential scheduling and resource conflicts for projects across therapeutic area/product assignments and provides recommendations to resolve.
Assists in selection, supervision, and project resourcing for writing support within assigned therapeutic area(s).
Accountable for meeting the main objectives of clinical writing projects in therapeutic area(s) within established timelines, budgets, and with an appropriate quality level.
Provides project management for writing projects for multiple compounds and/or indications within assigned therapeutic area, ensuring accuracy and adherence to timelines and processes.
Works directly with team members to develop/implement timelines to meet desired project completion dates and coordinates activities and communication with functional areas on writing projects.
Effectively collaborates with clinicians and management utilizing cross‑functional skills/expertise and scientific knowledge.
Proficiently learns and applies therapeutic area and product knowledge to scientific projects; develops expert knowledge of regulations, requirements, policies, and guidelines for writing projects.
Maintains and leads productive cross‑functional working teams, implements systems or solutions to enhance efficiency, eliminate redundancy, reduce expenditure, and guarantee quality.
Oversees writing projects to ensure timely completion, resolves conflicts, removes barriers, and generates innovative ways to ensure teams achieve project goals.
Continually trains/be compliant with all current industry requirements as they relate to assigned writing projects.
Qualifications
Bachelor’s degree in English or Communications with relevant science expertise or Bachelor’s degree in Life Science with relevant writing expertise; Advanced degree and/or professional certification preferred.
3 years relevant industry experience required; 5 years in medical writing in healthcare industry, academia, or related area such as quality, regulatory, publications, clinical research, or product support/R&D; 4 years in experimental design and clinical/preclinical data interpretation; 2 years in a project management role.
Form, maintain, and lead productive cross‑functional working teams; track record of collaboration and leadership.
Working knowledge of applicable regulations and legislation.
Excellent business communication skills with aptitude for summarization and detail orientation.
Experience developing and delivering presentations to senior management.
Ability to understand and interpret medical data and create strategic messaging.
Knowledge of product therapeutic area preferred.
Microsoft Office and Internet navigation proficiency; working knowledge of statistical concepts; other business‑related IT proficiency.
Identify and employ rigorous logic and methods to solve problems independently; recognize potential scheduling/resource conflicts and provide solutions.
Benefits and Compensation
Comprehensive benefits package including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) for eligible employees.
Eligibility to participate in short‑term and long‑term incentive programs.
Base pay range (subject to geographic location) and potential for additional compensation.
Equal Opportunity Employer, veterans/disabled accepted.
Equal Opportunity Statement AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Marketing, Public Relations, and Writing/Editing
Industry: Internet News
#J-18808-Ljbffr