Pfizer Senior Manager, Content Management and Authoring in Groton, Connecticut


Content Management and Authoring Senior Manager is accountable for providing leadership and subject matter expertise in the management and execution of Content Management and Authoring solutions. The incumbent will work with clinical, regulatory and safety functional lines and BT partners to identify and deploy advanced CMA solutions that promote authoring and process automation.


  • Champion automation across the organization, identify new opportunities, oversee active projects and day-to-day operations execute projects through successful deployment.

  • Collaborate across CMA, IM and BT to connect automation opportunities throughout business processes

  • Develop vision for how authoring and process automation can be deployed across the organization.

  • Establish a framework for measuring the value of automations.

  • Establish a framework for continuous improvement of automations for regulatory.

  • Establish and lead appropriate governance to engage CMA stakeholders in prioritizing opportunities for automation

  • Drive innovation in automation practices by leading a collaborative program of continuous improvement.

  • Partner with BT to interface with strategic products and services vendors to understand and influence products and platforms direction, usability, features and performance to assist business efficiency and quality.

  • Take maximum advantage of new technology by proactively engaging in partner groups to explore new solutions.

  • Lead/facilitate development of solution test strategies and user acceptance testing approaches during system releases to ensure high quality systems


  • BS/MS in Information Science, Life Sciences, Business or a related discipline with a comprehensive understanding of data and systems used in the R&D processes.

  • Graduate degree preferred

  • Minimum 5 years pharmaceutical industry experience in (or supporting) any of the following disciplines: clinical drug development, clinical trial management, safety surveillance and reporting, clinical project management, R&D or regulatory reporting and analytics, or regulatory affairs. Related experience in other industries will be considered.

  • Excellent analytical skills with demonstrated ability to investigate and solve problems

  • Minimum of 5+ years of project and/or program management experience

  • Knowledge of application system management and change control processes, application validation and implementation in a GxP environment.

  • Knowledge of Pharmaceutical metadata and standards

  • Experience with query tools/data extraction techniques (e.g., SQL, PL/SQL, Brio, MS_Access) is a plus.

  • Demonstrated customer relationship skills and capabilities to collaborate with teams.

  • Experience working with international colleagues, with skills to understand and present the "big picture" in terms of potential implications

  • Ability to communicate complex information and analyses to a variety of audiences in both verbal and written format

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.