Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. 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.
What You Will Achieve
You will ensure that the clinical studies conducted in the Pfizer Biopharma Group are within time, budget and scope. You will help us plan and direct the clinical studies. You will create the timelines of the study and also communicate these timelines to the team. Your ability to meet agreed targets will us develop plans for short-term work activities like deliverables, workplan and timelines.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Supervise and perform real time study activities and data collection as needed including mobile medical unit clinical activities.
Responsible for developing protocol based on protocol synopsis from Network Information Server Lead in consultation with PMS Safety Officer.
Provide support to the relevant medical functions in the management of studies.
Represent NHCRU clinic as Subject Matter Expert for various special projects.
Lead efforts in comprehensive reviews and provides expert clinical input on draft study protocols and Informed Consent documents.
Provide study specific protocol expertise and input on project planning, timelines, execution, and implementation as well as acquisition of specialty equipment.
Accountable for clinical oversight, subject safety, and regulatory compliance during shift operations including weekends and off-shift hours.
Provide technical expertise and assistance in managing biometric Subject Verification System.
Provide visitors from within and outside of company tours of clinic space and mobile medical unit and gives pointed specifics on clinic functionalities.
Qualifications
Must-Have
Bachelor's Degree
3+ years’ experience
Experience in public speaking and delivery of scientific, medical, and nursing educational presentations
Proven audit experience including preparation, development, follow-up and remediation plan
Proficiency and expertise in using Subject Verification System
Technical expertise and proficiency in various clinical skills
Demonstrates understanding of clinical research process
Good organizational skills and ability to prioritize
Excellent command and fluency in English language
Nice-to-Have
Master's degree
Relevant pharmaceutical industry experience
Work experience in clinical research trials, i.e. as a clinical research nurse, data collector, clinical research technician, study coordinator, or Data Manager
Experience with Electronic Data Capturing Management System platform
Other job details
Work Location Assignment: On-site 2-3x/week or as needed by the business
Last day to apply for job: November 13th, 2024
EEO (Equal Employment Opportunity) & 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, or disability.
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