Associate Medical Expert

108,000 people reimagining medicine for more than 799 million people globally. Be part of this journey by representing a group that delivers medical communication solutions across multiple franchises, business units and affiliates. Our services and customized solutions enhance the reach of clinical data about relevant therapeutic advancements and supports in right treatment decisions. We support scientific writing, medical communications plan development, innovative ways of evidence dissemination, supporting our colleagues in medical affairs organization.
- Your responsibilities include, but are not limited to:
- Build and maintain a strong business colleague focus and collaboration with NGSCs as well as Global Product Leads and Global Process Owners to represent voice of business colleague in service development and delivery
- Attend meetings with Novartis Scientific and Medical organizations and other scientific committees and on business colleague’s request participate in meetings with external experts/investigators and key opinion leaders.
- Provide scientific and medical expertise during regulatory agency inspections and internal audits for T&MO supported projects. Contribute to continuous service improvement initiatives in M&CS
- In collaboration with appropriate Clinical Trial Team (CTT) members: ensures direct medical support for assigned interventional and non-interventional studies as needed and may act as medical monitor:

- Contributes to development of study protocol and regulatory documents - Investigator’s Brochures, Health Authority briefing books, safety updates, submission dossiers, and responses to Health Authorities, supports medical review, reporting of quality data, and study reporting/publishing in compliance with Novartis processes, GCP/ICH, and regulatory requirements.
- Provides clinical leadership and medical input for clinical deliverables in assigned protocol(s).
- Contributes to clinical/scientific content of clinical communications and publications related to assigned trial(s). Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentation.

**Commitment to Diversity & Inclusion**:

- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

**Minimum requirements**
- Minimum science degree or equivalent, B.Sc./equivalent with 6 years Clinical Research (CR) experience, M.Sc./M.Pharma +4 years of clinical research (CR) experienc
- Desired - Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent)
- PhD + 2 year of CR experience, MBBS/equivalent + 2 year of
- CR experience, MD +1 year of CR experience
- Excellent written and oral English

Why Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.
We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying
Imagine what you could do here at Novartis
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

**Division**
- CTS

**Business Unit**
- CONEXTS

**Country**
- India

**Work Location**
- Hyderabad, AP

**Company/Legal Entity**
- Nov Hltcr Shared Services Ind

**Functional Area**
- Research & Development

**Job Type**
- Full Time

**Employment Type**
- Regular

**Shift Work**
- No

**Early Talent**
- No