Clinical Study Team Lead
3 weeks ago
Why Patients Need You
Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
Join us, and be a part of a team that values innovation, collaboration, and the relentless pursuit of excellence. Together, we can lead the way in healthcare and make a lasting impact on society.
What You Will Achieve
As a Clinical Study Team Lead (CSTL), you will be an integral member of Pfizer's clinical development team and a matrix leader accountable for study team delivery of multiple complex global studies and/or programs. Your clinical development expertise in the execution of obesity clinical trials will enable contributions to the design and conduct of obesity clinical studies in alignment with the program and portfolio strategies for the Internal Medicine Therapeutic Area. Your project management skills will be leveraged to develop clinical trial timelines and oversee budgets for the assigned clinical studies/programs. Your ability to partner and collaborate with functional line leadership will be instrumental in ensuring optimal resourcing of the study teams. While managing complex project environments, you will anticipate potential project risks and influence teams to develop proactive risk management and inspection readiness plans. In this role, your strong leadership skills and clinical operations expertise will help make Pfizer ready to achieve new milestones and help patients across the globe.
ROLE RESPONSIBILITIES
Study Team Leadership
Lead study teams and associated deliverables across all functions; accountable for managing and driving overall study timelines, budgets and quality targets to meet or exceed business needsAccountable for strategic planning and decision making at the study-level in line with program objectivesRepresents the study team at appropriate medicine team and sub-team discussionsPartner and collaborate with functional line leadership to ensure optimal resourcing of the study teamsDrive functional lines to ensure inspection readiness; ensure maintenance and accuracy of Standard Operating Procedures (SOP) logMaintain active awareness and appropriate escalation of all Significant Quality Events (SQEs) reported for study and ensure appropriate prioritization and management of events through to resolutionUtilize negotiation, facilitation, meeting management, and conflict resolution skills to enhance cross-functional study team performance and be accountable for effective study team operationsAccountable for issue escalation and resolutionLead study team chartering and team health check process
Governance & Decision Points
Drive proactive planning to navigate the team through governance and decision point milestones to support on-time delivery of study to maintain development timelinesDevelop and lead execution of data and document delivery plans at key milestones such as Proof of Concept and Phase 3 decisionsLead preparations for and present the study to relevant governance per organizational norms and expectations
Risk Management
Proactively identify operational issues and lead the teams in identifying options to de-risk and capitalize on opportunitiesLead the study teams in proactive problem solving, management and communication of risk management plans including risk assessment and mitigation strategies
Study Metrics & Reporting
Act as a single, authoritative source of study information and lead study-level status reporting per organizational norms and expectations; ensure systems are maintained with up-to-date program status, risks, and issuesOversee operational metrics across study(-ies) and partner with functional lines to manage trendsAccountable for managing overall submission of Clinical Development & Operations sub-team timelines, budgets, and quality targets
Submissions
Ensure comprehensive operational input to submission planLead cross functional Module 2/5 submission sub-teams with accountability for delivery and overall operational strategy to ensure data and document delivery to support submissions and rapid response. Manage other submission activities as necessaryOversee operational metrics across submission sub-teams and manage trends and escalations
BASIC QUALIFICATIONS
Training and Education:
Bachelor's degree (BS/BA) in science, health-related field or epidemiology, or a discipline related to drug development or business required10+ years of relevant experience (prior clinical trial, non-interventional study and/or epidemiologic study)
Prior Experience:
Extensive experience in conduct of multiple obesity clinical trials and clinical trial operations with glucagon-like peptide-1 (GLP-1) agonists and/or glucose-dependent insulinotropic polypeptide (GIP) compounds strongly preferred.Broad experience in a Clinical Trial Execution discipline (e.g. senior study management expertise, lead data management expertise, clinical leadership expertise)Demonstrated project management and cross-functional leadership experience associated with project and study management, knowledge of Good Clinical Practices (GCPs), monitoring, clinical, and regulatory operations requiredDemonstrated experience in understanding key drivers impacting budgets, building Clinical Trial Budgets and managing project to budgetDemonstrated breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact
Skills:
Strategic thinking and targeted problem-solving skillsExceptional communication and interpersonal skillsAbility to lead cross-functional teams, identify, resolve, and escalate issuesAbility to influence and collaborate with peersAbility to leverage, negotiate, and resolve conflicts to enhance team performance and deliveryAbility to represent & communicate clearly to senior leaders and governance bodiesAbility to understand and assimilate high-level data from all functions
PREFERRED QUALIFICATIONS
Advanced degree
Relocation support available
Work Location Assignment:On premise (flexible with office location)
#LI-PFE
The annual base salary for this position ranges from $161,600.00 to $269,400.00.* In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
* The annual base salary for this position in Tampa, FL ranges from $145,400.00 to $242,400.00.
Relocation assistance may be available based on business needs and/or eligibility.
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.
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. This position requires permanent work authorization in the United States.
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