Senior Manager, Value Writing

North Chicago, IL - USA

Monthly Salary: Not Disclosed

Posted on: 2 days ago

Vacancies: 1 Vacancy

Job Summary

Serve as the leader of cross-functional Publications Team(s) for assigned assets including leading team meetings/discussions and driving the execution of publication plans incorporating input from key global stakeholders
Lead tactical execution of publication plans (ie clinical manuscripts abstracts posters and oral presentations) meeting established timelines and budgets
Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications
Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics
Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets
Provide managerial oversight to internal and external medical writers regarding assigned projects ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures
Provide direction to external vendors to effectively complete the execution of publication projects within specified timelines and ensure quality publication deliverables
Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback resolve personnel issues and manage talent retention for assigned staff
Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date

Qualifications :

Minimum of Bachelors Degree required. PhD PharmD Masters Degree preferred. Relevant professional certification/credential (eg CMPP AMWA) is a plus.
4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg medical communication agency) experience required
Demonstrated abilities in a leadership capacity required
Ability to understand and interpret medical data require
Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required
Knowledge of clinical/scientific publication structure content and quality. Knowledge of scientific publication regulations and best practices
Excellent communication skills both written and verbal with demonstrated success in creating and delivering effective presentations to senior-level audiences
Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record
Ability to form maintain and lead productive cross-functional working teams including addressing issues that arise
Microsoft Office and Internet navigation proficiencies essential

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at thetime of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic locationand we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of anybonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys soleand absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.

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.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Yes

Employment Type :

Full-time

Serve as the leader of cross-functional Publications Team(s) for assigned assets including leading team meetings/discussions and driving the execution of publication plans incorporating input from key global stakeholdersLead tactical execution of publication plans (ie clinical manuscripts abstracts...

Serve as the leader of cross-functional Publications Team(s) for assigned assets including leading team meetings/discussions and driving the execution of publication plans incorporating input from key global stakeholders
Lead tactical execution of publication plans (ie clinical manuscripts abstracts posters and oral presentations) meeting established timelines and budgets
Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications
Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics
Partner with Publications Director to project and manage outsourcing budget and internal resource needs for assigned/assets
Provide managerial oversight to internal and external medical writers regarding assigned projects ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures
Provide direction to external vendors to effectively complete the execution of publication projects within specified timelines and ensure quality publication deliverables
Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback resolve personnel issues and manage talent retention for assigned staff
Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date

Qualifications :

Minimum of Bachelors Degree required. PhD PharmD Masters Degree preferred. Relevant professional certification/credential (eg CMPP AMWA) is a plus.
4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (eg medical communication agency) experience required
Demonstrated abilities in a leadership capacity required
Ability to understand and interpret medical data require
Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required
Knowledge of clinical/scientific publication structure content and quality. Knowledge of scientific publication regulations and best practices
Excellent communication skills both written and verbal with demonstrated success in creating and delivering effective presentations to senior-level audiences
Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Collaborative teamwork and leadership track record
Ability to form maintain and lead productive cross-functional working teams including addressing issues that arise
Microsoft Office and Internet navigation proficiencies essential

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at thetime of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic locationand we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

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.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Yes

Employment Type :

Full-time

Key Skills

Program Management
FDA Regulations
Management Experience
Facilities Management
Clinical Development
Data Management
Quality Systems
Project Management
Research & Development
GLP
Budgeting
Leadership Experience

Apply Now

About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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