Why Patients Need You

Medical Research Project Leads (MRPL) play a key role in project operation in Non-Interventional Study (NIS) including Post Marketing Surveillance (PMS) in Korea. This role is 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 non-interventional studies conducted in the Pfizer Chief Medical Affairs Office, RWE Platform are within time, budget and scope. You will help us plan and direct the studies. You will create the milestones 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 study operation lead, 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.
• Responsible for project operation including vendor, site, budget and quality management in consultation with NISL (Non-Interventional Study Lead).
• Provide support to the relevant functions in the management of studies.
• Represent a study operation lead as Subject Matter Expert for various special projects.
• Lead efforts in comprehensive reviews and provides expert operation input on all stage from project plannin to publication.
• Provide study specific expertise and input on project planning, timelines, execution, and implementation as well as acquisition of specialty equipment.
• Accountable for study oversight, subject safety, and regulatory compliance during shift operations including weekends and off-shift hours.

Qualifications

Must-Have

• Bachelor's degree preferably in biological science, pharmacy or nursing
• 5+ years’ experience in study operation
• Experience in Non-interventional study operation including PMS in Korea
• 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

• Relevant pharmaceutical industry experience
• Work experience in clinical research trials, i.e. as a clinical research nurse, data collector, clinical research technician, study coordinator
• Experience with Global communication

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