14 days old

Associate Director, Site Intelligence Lead

San Diego, CA
This role can be done remote anywhere US or Canada. Or based onsite at our offices in Groton, CT, New York, NY or Collegeville, PA


+ Partners with Clinical Operations to develop and deliver Site Intelligence plans.

+ Performs tasks for multiple Site Intelligence projects.

+ Supports Study Optimization Leadership/Head of Site Intelligence on special projects

+ Leads and/or participates in global initiatives to improve operational efficiencies.

+ Works under close supervision of Head of Site Intelligence


+ Supports, manages processes relating to Country & Site Intelligence.

+ Maintains continuity connecting and documenting work performed by the Feasibility Lead in Early Estimates, Early Feasibility, Detailed Assumptions, Detailed Feasibility, to Site Selection.

+ Supports the build of the investigator database, collection of information supporting the definition of the ideal site for a study, identification of suitable sites for a study, and coordinates global efforts for site intelligence.

+ Acts as primary contact for the study team in the Site Intelligence process. Participates in the Site Intelligence by leading the preparation of the country plan for the study (number of sites proposed, type of sites, recruitment rates, and key challenges) coordinating site intelligence resources to ensure timely completion of tasks and high quality.Engages with therapeutic business units to support and deliver the implementation and delivery of specific Site Intelligence initiatives through good communication, clear implementation plans and explicit performance metrics to

+ agreed timelines and quality,

+ Creates awareness by working as a cross functional team leader to deliver Site Intelligence initiatives with a variety of stakeholders, both internal and external. Initiatives will be diverse and may include technology and process improvement components.

+ Supports and maintains to the development of relevant information libraries and communication materials to assist with Site Intelligence activities.

+ Additionally runs operational and technical aspects of large global projects and assists with other Company systems activities related to the Site Intelligence.

+ Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity

+ Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery

+ Support governance processes by providing site intelligence information leveraging existing data sources and organizational knowledge/expertise.

+ Partners with Alliance Partners, Global Head of SSU, DevOps teams, and RU/BU partners to improve overall study start up metrics and implement simple processes.


+ In general, candidates for this job would have the following levels of experience in Clinical Research/Clinical Operations: BS/Equivalent - 8 years, MS - 6 years, PhD

+ Experience in a clinical research organization and related therapeutic specialties with familiarity in principles, concepts, practices and standards. Feasibility experience is a must.

+ History of success in a customer service role with demonstration of meeting customer expectations.

+ Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, database applications)

+ Strong presentation skills, interpersonal skills, as well as a team oriented approach. Excellent verbal, written, communication and time management skills

+ Ability to multitask under tight deadlines on several projects with specific and unique requirements, while providing attention to detail and high quality work.

+ Demonstrated knowledge of clinical research processes and regulatory requirements.

+ Demonstrated success/results in prior roles including matrix organization

**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.


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Associate Director, Site Intelligence Lead

San Diego, CA

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San Diego, CA

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