3 Medical Consulting jobs in Thailand

0.8 million. This is the number of patients in Thailand that across 57 Novartis brands have reached. We are also one of leading Pharmaceutical companies in Thailand who invest in Clinical Trials.
- We are on our journey to reimagine medicine and our team focus on delivering healthcare solution which fit for purpose. We strive to be the best place to work where our associates could be their best self each day and every day to unleash their full potential.
- We are looking for individual to join our team who have passion to improve and extend people’s lives.**Your Responsibilities**:
Your responsibilities include, but are not limited to:
- Support country medical affairs strategy in line with the global strategy, country insights and market conditions, and implementation of Medical Affairs activities within the designated therapy area(s).
- Coordinate scientific meeting, symposia, congresses, Continuous Medical Education (CME) and other medical / scientific exchange and engagement activities which could bring value to the therapy area; develop engagement plan(s) for country customer-facing activities and events, and ensure timely execution of the activities in an efficient and compliant way.
- Ensure enquiries are responded to in a quality, timely manner, and in accordance with applicable standards; establish response documents for frequently asked questions.
- Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the therapeutic area. Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities.
- Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for partner engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines.
- Ensure medical insights are provided to cross-functional groups, including, but not restricted to: Pharmacovigilance, Regulatory Affairs, Market Access, QA, Commercial and Brand team and others.
- Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.

**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**

**What you’ll bring to the role**:

- Education in MD, or PhD degree in health sciences required
- Fluent in Thai and English (oral and written)
- More than 2 years’ experience in clinical medicine and/or research.
- Medical and scientific writing skills.
- Knowledge of assigned therapeutic area with ability to interact with medical experts.
- Familiar with all aspects of drug development, GCP and local regulations, including regulations of Pro-motional materials.
- Knowledge of clinical trial design statistics and pharmacokinetics.
- Familiar with marketing principles and strategies.

**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!**Division**
- PHARMA

**Business Unit**
- AMAC

**Country**
- Thailand

**Work Location**
- Bangkok

**Company/Legal Entity**
- NOV THA

**Functional Area**
- Research & Development

**Job Type**
- Full Time

**Employment Type**
- Regular

**Shift Work**
- No

**Early Talent**
- No

**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Medical Advisor, Oncology & Hematology in Thailand.
**Live**
**What you will do**
**Accountabilities**
The Medical Advisor is a point of medical contact for Amgen's CDx strategy and pipeline/life-cycle Oncology & Hematology portfolio. The Medical Advisor leads adaptation of global & regional strategy to reflect local/regional priorities and supports implementation of those strategies toimprovee Amgen's value proposition in alignment with product strategies.
**Responsibilities**
+ Support development and implement of patient-focused medical strategies that improve the value proposition of Amgen's therapies including annual strategic planning and goal setting, launch support and lifecycle management, in collaboration with Country Medical Lead and/or Regional Medical TA Head, appropriate cross-functional teams and governance
+ Contribute to cross functional stakeholder teams in shaping the healthcare ecosystem by enabling access to medicines through evidence generation, communication and education of medical and economic value
+ Synthesize and integrate insights to deliver medical inputs into relevant cross-regional /functional strategies, including relevant brand strategy
+ Foster and enhance collaboration and coordination across Medical
+ Contribute to strategy development for scientific engagement across a broad range of collaborators to strengthen external understanding of the unmet need and value of the product
+ Lead/support relationships with external healthcare community, including interactions with opinion leaders, payers and societies for scientific exchange, where appropriate
+ Develop/support and lead/support implementation of the strategy for medical evidence generation that shapes our products and informs the practice of medicine ensuring key needs are met in alignment with global product medical and relevant brand strategy
+ Foster Amgen's reputation as a science-based, innovative and patient-focused reliable partner
+ Develop and/or contribute to implementation of advocacy plans and strategies in partnership with internal collaborators and lead relationships as appropriate
+ Partner with/support Global Regulatory Affairs and Safety (GRAAS) in risk management/minimization activities and ensure communication of the implications to internal/external collaborator
+ Member and Medical representative of relevant leadership, governance and cross functional teams
+ May develop and manage medical product budget
+ Coach, mentor, motivate and develop talent, as appropriate
+ Ensure conduct of medical activities in full compliance of all laws, regulations and SOPs
+ Ensure product/disease state/pipeline specific medical training where appropriate, may deliver training to others
+ Ensure appropriate clinical trial conduct as a key medical interface in close partnership with Global Development Operations (eg Site Management)
+ Provide strategic input into labels/regulatory/reimbursement/policy/promotional used to support internal/external interactions
+ Determine scientific/medical subject matter appropriateness of labels/regulatory/reimbursement/policy/promotional and medical deliverables (eg, slide decks, publications, educational activities) used to support internal/external interactions via appropriate review process
+ Contribute to strategy development for, review, approve and ensure dissemination of, medical communications and related activities (eg, product narrative, scientific platform, core content, publications including FPR/FLR, medical education and congresses)
+ Provide support and leadership of advisory boards and other relevant meetings (eg, investigator meetings, and/or expert panels)
+ Lead/support the development of data interpretation, analysis and communication for medical executed studies
+ Provide decision on IME, Donations, medical grants and sponsorships, where appropriate
+ Use global infrastructure for tracking, measuring and evaluating performance and ensure continuous performance improvement
+ Understand the expectations of key external collaborators to support appropriate access to Amgen therapies.
+ In partnership with cross-functional team, ensure informed budget/resource trade-offs, as appropriate
+ Facilitates Investigator Sponsored Studies through Amgen governance and manage study lifecycle (including communicating with investigators, as appropriate and ensuring accurate reporting of key milestone data)
+ Contribute to lifecycle management plan
**Win**
**What we expect of you**
**Minimum Requirements**
+ Doctorate degree & 3 years of directly related experience
+ Bachelor's degree & 6 years of directly related experience
**Preferred Requirements**
+ Demonstrated ability as a medical expert in a complex matrix environment
+ Pharmaceutical product development, product lifecycle and commercialization process knowledge with understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Safety, Regulatory, Value & Access, and Medical Affairs
+ Product/therapeutic area knowledge
+ Experience in regional/local medical practice and healthcare ecosystems
+ Skilled at engagement, scientific exchange with external medical community
+ Clinical research experience
+ In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
+ Familiarity with concepts of clinical research and clinical trial design, including biostatistics
+ Sound scientific and clinical judgement
+ Knowledge of Good Clinical Practices (GCP), region regulations and guidelines, and applicable international regulatory requirements
+ Familiarity of local pharmaceutical industry and legal/health system environment
+ Skilled at effectively presenting ideas and documenting complex medical/clinical concepts in both written and oral communication
+ History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
+ Network of medical, clinical contacts in product/therapeutic area
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
Apply now
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.