Manager/Senior Manager-Medical Information

Soterius, Inc.; Uttar Pradesh; On-site; INR 2,500,000 - 5,000,000; Full time

Benefits offered by this job

Career progression

Leadership exposure

Team-building opportunity

Flexible work arrangements

Job summary

Soterius, Inc. in India is seeking a Manager, Medical Information to oversee sponsor accounts and MI operations. You will lead a small team, develop SOPs, and partner with PV and Quality to ensure quality and compliance across programs.

The role offers remote, full-time engagement with opportunities to influence process improvements, content strategy, and global client delivery, while advancing your leadership capabilities within a growing organization.

Qualifications

• 10+ years in life sciences with MI and/or PV.
• Experience leading MI teams in CRO/pharma.
• Proven track record managing client SLAs and audits.
• Experience coordinating across global markets.

Responsibilities

• Lead end-to-end MI delivery for sponsor clients under SLAs.
• Oversee quality, timelines, and regulatory compliance.
• Recruit, coach, and grow MI Associates and Specialists.
• Develop SOPs, content libraries, and knowledge management.

Skills

MI management

PV expertise

Client relationships

Audit readiness

Education

PharmD

M Pharm

Tools

MI databases

Content management systems

Job description

Manager/Senior Manager-Medical Information

3-6 years

Remote

Full-Time

Why this role exists

We are seeking a Manager, Medical Information to support the delivery and continued development of our Medical Information services. This role will be responsible for overseeing sponsor accounts, ensuring high-quality and compliant MI operations, and contributing to process and team development within a growing organisation.

The position offers the opportunity to work closely with leadership, cross-functional teams, and clients, while helping shape scalable and efficient ways of working across the MI function.

Why this matters for you

This role is ideal for someone looking to take on broad operational responsibility and contribute beyond day-to-day delivery.

In this role, you will:

• Manage sponsor accounts with end-to-end oversight of Medical Information activities
• Support team growth, capability building, and operational excellence
• Contribute to process improvements, SOP development, and technology-enabled solutions
• Partner with internal stakeholders during program planning and business discussions
• Apply your Pharmacovigilance (PV) experience to support effective collaboration across MI and PV activities

While the title is Manager, the role offers significant exposure to client engagement, operational strategy, and functional development within a dynamic and evolving environment.

What you will own

Service delivery and client ownership

• Lead end-to-end MI delivery for assigned sponsor clients, ensuring adherence to contractual SLAs, applicable regulations, and global guidance
• Act as the primary point of accountability for quality, timelines, and compliance across your portfolio
• Handle and oversee medical enquiries from HCPs, patients, consumers, and other stakeholders across phone, email, and other channels, including non-IST coverage where required
• Own quality control of MI responses, escalations, and adverse event and product complaint handoffs to PV and Quality

Function building and team leadership

• Line-manage a small team today, with a clear mandate to grow and shape it as the function scales
• Recruit, onboard, coach, and develop MI Associates and Specialists
• Identify skill gaps, design training plans, and raise the technical and scientific bar of the team
• Manage workload distribution and flag risks to leadership before they become quality or delivery issues

Content, systems, and continuous improvement

• Author and review SOPs, work instructions, and controlled documents for the MI function
• Lead development and lifecycle management of Standard Response Documents, FAQs, and global content libraries
• Own MI project setup, database configuration, validation, and onboarding for new client engagements
• Contribute to how we use technology, automation, and AI to make MI delivery faster and better, without compromising scientific rigour

Compliance, audits, and stakeholder engagement

• Represent the MI function during sponsor audits, regulatory inspections, and internal quality reviews
• Maintain a clean compliance posture across documentation, training, and CAPA
• Partner with PV, Quality,

What we are looking for

Experience

• 10+ years in life sciences, with demonstrable depth in Medical Information, Pharmacovigilance, or a combination of both
• Prior MI management or MI team-lead exposure in a CRO, pharma, or biotech setting
• Track record of managing client relationships, SLAs, and audit readiness, ideally across multiple sponsors or therapy areas
• Experience handling medical enquiries across global markets and time zones

Skills and qualifications

• Life sciences or pharmacy degree; PharmD, M Pharm, or equivalent advanced qualification preferred
• Strong working knowledge of MI and PV regulations, ICH guidelines, and global pharmacovigilance frameworks
• Comfortable authoring SOPs and controlled documentation
• Hands-on familiarity with MI databases and content management systems

How you operate

• You take ownership and do not wait to be told what to escape
• You hold a quality bar without becoming a bottleneck
• You can coach a junior associate one hour and brief a sponsor lead the next
• You are curious about where the function is going, not just how it runs today

What we offer

• A clear and visible career path. This role is set up to grow into Senior Manager and beyond as the function expands
• Direct exposure to leadership, clients, and the commercial side of the business
• The chance to build a team rather than maintain one
• Competitive compensation, with structured performance reviews and growth planning
• Flexibility on working arrangements where the role permits