Pfizer Hiring PV Aggregate Reports Analyst in Chennai

Pfizer, a global pharmaceutical leader, is seeking a skilled Aggregate Reports Analyst to join their Worldwide Safety department in Chennai, India. At Pfizer, we are committed to making the world a healthier place, and you can be a part of our mission to connect evidenced-based medical decision support with healthcare stakeholders to enhance patient well-being.

Vacancies List:

• Company Name: Pfizer
• Company Address: Chennai, India
• Position Title: Aggregate Reports Analyst
• Role: Aggregate Reports Analyst
• Department: Worldwide Safety
• Industry Type: Pharmaceutical
• Employment Type: Full-Time
• Role Category: Healthcare

Job Description:

As an Aggregate Reports Analyst at Pfizer, you will have the responsibility of creating crucial documents to support product development, license applications, and post-marketing maintenance. Your role will involve accurately translating regulatory requirements into timely and compliant safety data analysis and presentations. This ensures informed healthcare decisions regarding the use of medicines for patient safety.

Key Experience Offered by this Role:

As an Aggregate Reports Analyst, you will enjoy:

• Being a part of the Aggregate Report Center of Excellence team.
• Collaborating with experienced colleagues worldwide.
• Liaising with key partners from different sites.
• Identifying potential process improvements.
• Serving as a point of contact for document issues.
• In-depth training and mentoring.
• A dynamic work environment with growth potential.

Primary Responsibilities:

Your responsibilities will include:

• Preparing integrated analyses of safety data to support aggregate reports and regulatory queries.
• Communicating department’s position on resource and timeline needs.
• Ensuring documents are produced in accordance with internal SOPs and regulatory guidance.
• Driving document strategies and messages in collaboration with subject matter experts.
• Providing oversight for internal or external co-authors when required.
• Understanding relationships between documents and analyses produced for regulators.

What You Offer:

Basic Qualifications:

• Bachelor’s Degree in life sciences and 3+ years’ relevant medical experience such as, patient care, clinical trial experience / investigator, academic medicine, specialty training or pharmaceutical industry experience, ideally in safety, regulatory or clinical areas
• High fluency in written and spoken English.
• Excellent scientific writing skills.
• Ability to examine data and formulate hypotheses.
• Familiarity with global regulatory guidance.

You are a self-motivated individual with strong organizational and interpersonal skills. You can effectively influence and negotiate, mentor junior colleagues, and make decisions in complex situations.

Preferred Qualifications:

• Advanced degree (MD, DVM, PharmD, or Master’s/PhD in relevant field).
• Experience with software used for data analysis.
• Proficiency in statistical concepts.
• Familiarity with epidemiologic principles.

Transferrable Experiences/Skills:

Experience in pharmacovigilance, regulatory affairs, or clinical work will be considered an asset.

At Pfizer, we uphold our values of Courage, Excellence, Equity, and Joy. Your work location will be flexible.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.