Instagram
youtube
Facebook

Safety Sciences Lead

6+ years
Not Disclosed
10 Feb. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety Sciences Lead – Amgen

Location: Hyderabad, Telangana, India | Job Type: Full-time | Category: Pharmacovigilance

Join Amgen’s Mission to Serve Patients

At Amgen, you’re part of something bigger—driving innovation to help patients with serious illnesses. Since 1980, we’ve pioneered biotech solutions across Oncology, Inflammation, General Medicine, and Rare Disease, impacting millions of lives.

Now, we’re looking for a Safety Sciences Lead to join our mission. If you’re passionate about drug safety, innovation, and leadership, this role is your chance to make a lasting impact.


About the Role

Your Mission

As the Safety Sciences Lead, you will oversee signal detection, risk management, and compliance at our India site, working closely with global teams. Your leadership will shape Amgen’s safety strategy while ensuring regulatory adherence and excellence in pharmacovigilance.

Key Responsibilities

Lead Signal Management: Oversee signal detection, analysis, and reporting to ensure patient safety.
Strategic Leadership: Drive Amgen’s global safety initiatives, ensuring compliance with EU, US, and ICH regulatory standards.
Team Development: Recruit, mentor, and manage a high-performing Safety Sciences team in India.
Cross-functional Collaboration: Partner with tech teams, global safety groups, and other stakeholders to enhance pharmacovigilance capabilities.
Operational Excellence: Optimize safety processes, prioritize resources effectively, and contribute to budget and headcount planning.
Continuous Improvement: Lead or contribute to cross-functional initiatives that elevate global safety strategies.


What We Expect from You

Basic Qualifications

🔹 Medical Degree with at least 6 years of experience in global Pharmacovigilance (clinical trials & post-marketing).
🔹 Minimum 3 years of leadership experience managing PV teams.
🔹 In-depth knowledge of global PV regulations (EU, US, ICH, GCP) and drug safety databases.
🔹 Strong project management & problem-solving skills, with the ability to manage multiple priorities.
🔹 Effective negotiation & strategic decision-making abilities.


What You Can Expect from Us

At Amgen, we invest in your success:
Competitive Compensation & Benefits aligned with industry standards.
A Collaborative, Science-Driven Culture that fosters innovation.
Growth & Development Opportunities to advance your career.
Inclusive & Diverse Work Environment that values every individual.

📌 Apply Now: Be part of a career that defies imagination and transforms lives.

🌍 Explore Opportunities: careers.amgen.com