久久久久久久久免费_久久久久久久久网站_久久久久久久久一区_久久久久久久网_一级免费在线_一级女人真人毛片免费看

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 be relied on by the company to monitor its drug, biologics and
medical devices surveillance program. This will include intake, evaluation and
processing of the adverse reports received. You will support the clinical trial
as well as the post marketing activities.



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 dedication and hard work that will make it possible for Pfizer’s
customers and patients to receive the medicines they need, when they need them.



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.
* Provide oversight, team mentoring on case handling aspects, data extraction
and analyses and conduct follow-up activities.
* Act as subject matter expert and liaise with key partners regarding safety
data collection and data reconciliation.
* Review, analyze, prepare, and complete safety-related reports within scope
to determine the safety profile of Pfizer's products and to meet regulatory
requirements.
* Review processed cases to verify accuracy, consistency and compliance with
process requirements, and review case data for special scenarios.
* Manage, where applicable, safety resources in the local team.
* Provide specific pharmacovigilance or product knowledge and experience, as
required by the business, and mentor colleagues accordingly.
* Develop and maintain advanced knowledge of all products within the Pfizer
portfolio.
* Develop and maintain expertise of all assigned products, of applicable
corporate policies.
* Design and oversee the tracking of applicable safety metrics.
* Manage project and process management meeting established deadlines.
* And search functions in the safety database and data mart.


Qualifications

Must-Have

* Bachelor's Degree
* 3 years' experience
* Demonstrated organizational/project management skills
* Solid knowledge of global regulations and guidelines for drug development
* Demonstrated analytical and statistical skill.
* Ability to make decisions independently and resolve issues appropriately
* Strong skills in productivity, organizational and time management in order
to meet strict regulatory compliance goals
* Fluent in spoken and written English


Nice-to-Have

* Master's degree
* Relevant pharmaceutical industry experience
* Familiarity with management of performance metrics
* Ability to make decisions independently in both routine case processing and
unique and/or complex situations, and to resolve issues appropriately to
achieve a desired result or impact




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




Medical



#LI-PFE