Associate Director-Real World Evidence

3-8 years

Not Disclosed

Hyderabad

10 Nov. 26, 2025

Job Description

Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Associate Director – Real World Evidence (RWE)
Location: Hyderabad, India (Hybrid)
Job Type: Full-Time, Regular
Industry: Pharmaceutical / Life Sciences / Healthcare
Experience Required: Minimum 8 years in pharmaceutical, healthcare, or research sectors; 3–5 years in people management

About the Role

We are seeking a highly experienced Associate Director – Real World Evidence (RWE) to lead and expand our RWE operations in Hyderabad. This role is pivotal in executing Non-Interventional Studies (NIS) and generating high-quality Real-World Evidence to support strategic priorities in US Medical Affairs across multiple therapeutic areas. The Associate Director will oversee a team of RWE professionals, building internal execution capabilities while ensuring the timely delivery of scientifically rigorous studies.

The successful candidate will work in close collaboration with global teams based in the US and Ireland, contributing to evidence generation strategies that improve patient access, support clinical decision-making, and address key knowledge gaps.

Key Responsibilities

Operational Study Execution

Lead end-to-end management of RWE studies, including study design implementation, data analysis planning, and deliverable generation.
Ensure adherence to study protocols, timelines, and internal/external quality standards.

Team Leadership & Development

Manage and mentor 3–5 managers overseeing 12–15 research associates.
Foster professional development through coaching, training, and capability-building initiatives.

Quality Oversight

Maintain scientific rigor and compliance with regulatory and ethical standards.
Implement quality control processes, conduct project reviews, and drive continuous methodological improvements.

Internal Capability Building

Develop standardized processes, templates, and best practices for internal RWE study execution.
Build Hyderabad-based team capabilities to transition toward robust, internally executed studies.

Global Collaboration & Stakeholder Communication

Work closely with global colleagues and therapeutic area teams to deliver high-impact evidence generation outputs.
Provide clear and concise updates on project progress to RWE leadership and stakeholders.

Scientific Contribution

Support protocol development, statistical analysis plans, and research outputs.
Review and approve analytical approaches, results interpretation, and study reports to ensure scientific validity.

Project & Resource Management

Prioritize and allocate resources efficiently across multiple concurrent projects.
Track timelines, identify risks, and implement mitigation strategies to ensure timely delivery.

Qualifications & Experience

Minimum Requirements:

Bachelor’s degree in Life Sciences, Public Health, Epidemiology, Biostatistics, or related field.
Master’s, PhD, or advanced degree preferred.

Preferred Experience:

8+ years in pharmaceutical, healthcare, or research sectors with significant RWE experience.
3–5 years of people management experience, preferably managing managers or analytical teams.
Proven success in delivering complex studies from design through completion.
Experience in global, matrixed organizations, collaborating across geographies and cultures.

Technical Expertise:

In-depth knowledge of RWE methodologies, including observational study designs, comparative effectiveness research, and outcomes research.
Familiarity with common RWE data sources (e.g., EHRs, claims databases, registries, patient-reported outcomes).
Strong statistical and analytical expertise applied to RWE studies.
Understanding of regulatory, ethical, and compliance considerations in RWE generation.
Proficient in project management, timeline tracking, and resource allocation.

Leadership & Behavioral Skills:

Inspirational team leadership with focus on inclusion, coaching, and capability building.
Strong operational and project management skills to ensure accountability and timely results.
Excellent collaborative skills for working across global teams and matrix structures.
Problem-solving mindset with adaptability to changing priorities.
High standards for quality, scientific rigor, and stakeholder communication.

Why Join Novartis?

At Novartis, our purpose is to reimagine medicine to improve and extend lives. Our associates drive innovation every day, collaborating to deliver breakthroughs that transform patient care. By joining our Hyderabad team, you will contribute directly to strategic RWE initiatives that influence clinical decision-making and patient access globally.

Diversity & Inclusion: Novartis is committed to building diverse, inclusive teams reflective of the communities we serve.

Benefits & Rewards: Competitive benefits and development opportunities. Learn more in the Novartis Life Handbook.

Stay Connected: Not the right fit? Join our Novartis Talent Network to stay informed about future opportunities.

Apply Now to be a part of a global mission that is transforming the future of medicine.

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Associate Director-Real World Evidence

Job Description

About the Role

Key Responsibilities

Qualifications & Experience

Why Join Novartis?

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