Job Detail
-
Offered Salary 0
Job Description
Qualifications
- Bachelor’s Degree
- 7+ years’ experience
- Applicable pharmaceutical industry experience
- Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations
- Demonstrated project management / leadership experience
- Experience with CRO oversight
- Ability to evaluate, interpret and present complex issues and data to support risk
- Excellent communication skills, both written and verbal; must be fluent in English
- Effective decision maker, analytical and solution-oriented
- Proficiency in Microsoft Office Suite
- Master’s degree
- Broad based experience in clinical research
- Strong knowledge of Therapeutic Area, subject matter expertise and international experience
- Non-standard Work Schedule, Travel Or Environment Requirements
Benefits
- Eligible for Employee Referral Bonus
- The annual base salary for this position ranges from $109,400.00 to $182,300.00
- In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% 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)
- The United States salary range provided does not apply to Tampa, FL or any location outside of the United States
Responsibilities
- Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple
- Empower healthcare decisions regarding the safe and appropriate use of medicines for patients
- You will be part of Pfizer’s medical team and manage the clinical studies
- Your project management skills will be leveraged for planning, directing, creating and communicating timelines
- You will ensure that the clinical studies are within time, budget and scope
- As a Senior Manager, your advanced knowledge of the principles and concepts in the discipline and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division
- Your ability to develop and manage plans will facilitate in achieving objectives, interpreting internal and external business challenges and recommending best practices for improvements
- While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division
- It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe
- Develop ideas, lead/co-lead complex projects across business units and develop plans to achieve objectives
- Approve the Study Startup, Study Monitoring and protocol recruitment plans
- Resolve escalated issues identified by the site activation subteam in partnership with the Study Manager
- Work proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery
- Manage Operational Study Management for one or more studies of limited complexity or a unique part of a larger study
- Forecast and manage the Clinical Trial Budget for the program
- Provide country and regional level input to country outreach surveys
- Create awareness by working as a cross functional Team Leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external
- Approve and oversee drug supply management, manage flow of drug supply to the sites
- Participate in global initiatives to improve operational efficiencies
- Evaluate study progress reports and results for overall compliance and recommends corrective action or study termination for non-performance
- Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback
Apply Now
Application ends in 12d 4h 10min