Pfizer Pharma Safety Assistant Vacancy 2021 - Apply Online

Pfizer Pharma Safety Assistant Vacancy 2021 – Apply Online

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 the 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.

Job Title: Safety Assistant

Location: India – Mumbai

Qualifications

  • B. Pharm or graduation in Health Care domain preferred
  • Ability, with supervision, to solve routine problems and to surface issues constructively
  • Ability to make basic decisions with an understanding of the consequences
  • Ability to achieve personal objectives while meeting departmental standards of performance
  • Ability to work under supervision in a matrix organization
  • High attention to detail
  • High interpersonal skills
  • Fluency in spoken and written English

Reports to Country Safety Lead

Position purpose: Execution of local activities relevant to the management of safety data.

Primary Responsibilities

  • Maintain local documentation as required by legislation (including archiving/tracking/retrieval)
  • Support the submission and distribution of reports and the relevant tracking
  • Support distribution and tracking of distribution of FU letters
  • Support inspection preparedness activities
  • Consistently apply case receipt policies and practices as per Company SOP and support in case of processing in the global safety database
  • Consistently apply to archive policies as per Company SOP

Technical Skill Requirements

  • Demonstrated computer literacy, particularly in the use and management of relational databases
  • IT skills (Word / Excel)

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 an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
  • 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 project milestones and organize own work to meet project task deadlines.
  • Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.
  • Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.
  • Review case criteria to determine the appropriate workflow for case processing

Apply Online

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