Novartis
Senior Scientific Operations Manager
India · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerNovartis
- LocationIndia
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Job Description Summary
Working closely with the IMA and IMACE Teams to provide operational support for key IMA activities and processes for assigned TAs.
Job Description
Role Summary
The Project Manager, Medical Affairs Operations serves as the primary point of contact (POC) for assigned therapeutic areas and projects, driving end-to-end project execution, operational excellence, and stakeholder coordination. The role is responsible for managing project lifecycles, ensuring timely delivery, compliance adherence, process improvements, and effective collaboration across internal and external stakeholders.
Key Responsibilities
Project & Operational Management
Act as the primary POC for assigned therapeutic areas, projects, and operational processes.
Manage end-to-end project execution from initiation through completion, ensuring delivery against timelines, quality standards, and objectives.
Show full description
Coordinate FUSE submissions, internal medical meetings (e.g., IMATs), SharePoint maintenance, and distribution list management.
Oversee multiple projects simultaneously and ensure successful execution of assigned tactics and deliverables.
Maintain accurate project documentation, reporting, and stakeholder communications.
Provide proactive recommendations to improve project management and operational effectiveness.
Serve as a trusted advisor and subject matter resource for assigned projects.
Stakeholder & Cross-functional Collaboration
Partner with internal and external stakeholders to drive project execution and achieve business objectives.
Facilitate effective communication across cross-functional teams.
Build strong working relationships and ensure alignment on project priorities and deliverables.
Lead meetings and drive discussions toward actionable outcomes.
Operational Excellence & Leadership
Drive continuous improvement initiatives and operational excellence programs.
Identify, address, and resolve operational issues efficiently.
Promote innovation, best practice sharing, and process optimization across teams.
Ensure compliance with company policies, industry regulations, and approval processes.
Mentor and support team members, fostering knowledge sharing and capability development.
Essential Requirements:
Successful and timely delivery of projects against agreed timelines and objectives.
Achievement of defined operational and project management KPIs.
100% compliance with company policies, SOPs, legal regulations, and industry standards.
Implementation of initiatives that improve operational efficiency and effectiveness.
Desired Profile
Education
Postgraduate degree, preferably in a Science-related discipline.
MBA or equivalent qualification preferred.
Experience
Minimum 7 years of experience in project management and operations within the pharmaceutical industry or healthcare agencies.
Proven track record of managing complex projects and operational initiatives.
Experience working with digital solutions, innovation programs, and process transformation initiatives.
Exposure to multicultural and cross-functional working environments.
Skills & Competencies
Strong project and stakeholder management capabilities.
Excellent communication, presentation, and facilitation skills.
Ability to manage multiple priorities and deliver results in a fast-paced environment.
Strong business acumen and understanding of pharmaceutical industry operations.
Proven leadership, mentoring, and team development skills.
Strong interpersonal, problem-solving, and relationship management abilities.
High attention to detail with a focus on execution excellence and compliance.
Fluent in English, both written and verbal.
Ideal Candidate
A seasoned Project Management professional with pharmaceutical industry experience, capable of driving complex operational initiatives, managing diverse stakeholders, and delivering projects with excellence while fostering innovation, compliance, and continuous improvement.
Commitment to Diversity and Inclusion / EEO paragraph:
Novartis is committed to building an outstanding, inclusive work environment and diverseteams’representative of the patients and communities we serve.
Why Novartis:Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating,supportingand inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards:Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:https://www.novartis.com/careers/benefits-rewards
Skills Desired
Clinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Medical Information, Patient Care, Stakeholder Engagement
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- SenioritySenior
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.