What Jobs are available for Medical Advisor in Malaysia?
Showing 3 Medical Advisor jobs in Malaysia
Medical Advisor - Eyecare & Neuroscience (Singapore & Malaysia)
Posted 26 days ago
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Job Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Medical Advisor is responsible for the office-based and field activities in the TA in question. The Medical Advisor is responsible for supporting country AMD in addition to in country medical scientific liaison (MSL) activities, particularly the management of Medical and Scientific Information, Medical Affairs content facilitation and support to the commercial activities in Eye Care & Neurosciences in Singapore and Malaysia.
Reporting to the Medical Affairs Country Lead, Malaysia & Singapore you will be responsible for providing high level scientific and clinical support to external and internal customers, establishing and developing relationships with Key Opinion Leaders (KOLs) across the broad spectrum of products within this therapeutic area as well as in emerging indications.
You will be based in Malaysia and be responsible for field-based medical affairs activities within the therapy area; there is an expectation that more than 50% of the time will be spent in the field with healthcare professionals (HCPs).
Key Duties and Responsibilities
+ Provide in-depth scientific information on Allergan product data to HCPs upon request.
+ Deliver lectures/presentations on clinical and scientific topics, ensuring compliance approval.
+ Organize and deliver advisory board meetings with appropriate HCPs to stimulate scientific exchange with HCPs and gather business-relevant information
+ Assist in the organization and scientific support of key external events e.g. satellite symposia etc.
+ Organize and participate in external education and training events as appropriate.
+ Facilitate development of Investigator initiated Trials (IIT) Proposals in line with Allergan Strategy.
+ Facilitate and support publication of clinical data in line with Allergan Strategy.
+ Facilitate other research activities e.g. collection of real-world evidence
+ Establish and maintain relationships with KOLs across the therapeutic areas.
+ Identify and develop new KOLs in line with Allergan strategy.
+ Attend appropriate scientific congresses to interact with KOLs and develop knowledge regarding the wider therapy area and competitor information.
+ Collaborate with and involve selected KOLs in strategic advisory board meetings.
+ Develop KOL advocacy through provision of scientific and clinical information and involvement in appropriate medical affairs activities.
+ Develop and maintain high level of knowledge regarding therapy area and Allergan products including awareness of the competitive landscape.
+ Support the business unit by attending and contributing to national leadership meetings and working cross-functionally.
+ Provide guidance regarding appropriate speakers for national/international congresses and workshops to spread and enhance scientific exchange.
+ Organize clinical and scientific education as well as in-house training for Eyecare sales reps and other appropriate staff as required.
+ Develop country medical affairs plans in alignment with SEA cluster commercial plans
+ Contribute to scientific dossiers and reports where appropriate.
Qualifications
+ Medical Doctor, Ophthalmologist, Neuroscientist, Biologist, Chemist or Pharmacist with an MD, PharmD or PhD degree.
+ Pharmaceutical or medical devices industry background ideally in a field based scientific medical liaison or medical advisor position.
Essential Skills
+ Excellent verbal, written, analytical and interpersonal skills.
+ Experience of developing and maintaining relationships with international and local opinion leaders.
+ Excellent work ethic.
+ Able to understand and communicate clinical and scientific data.
+ Ability to conduct clear and concise scientific discussions at a high level.
+ Able to interact professionally and skillfully at all levels.
+ Clear strategic thinker; able to rapidly gain an understanding of the business and its competitive environment, with the ability to translate vision into action.
+ The ability to work in a dynamic, multicultural and matrix structure.
+ Goal and results orientated.
+ Drive, high energy, maturity, ability to work under pressure and deliver results to tight deadlines and in a rapidly changing environment.
+ Self-confident. Committed. Entrepreneurial and creative. Able to decide "right and fast" based on the data analysis and own experience.
+ Ability to work autonomously and a good team player.
+ Strong personal management and organizational skills include time management, workload prioritization, responsiveness, multi-tasking and flexibility.
+ Flexibility and ability to travel frequently.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
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Medical Affairs Manager
Posted 26 days ago
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Job Description
+ The Medical Manager is accountable for providing input into the development and delivery of a strategic, regionally and globally aligned medical activity plan in Malaysia in order to deliver improved therapeutic benefit for the patient.
+ The incumbent will be responsible for Affiliate Medical Affairs, Clinical Research and Pharmacovigilance activities and will be a medical subject matter expert supporting Regulatory Affairs, Business Development, Quality Assurance and Commercial when necessary.
+ This position coordinates and executes local medical and clinical research initiatives, enables and assists the affiliate to provide quality local medical services to EPD Strategic Medical Affairs (SMA).
**Core Job Responsibilities:**
Oversee medical aspect of brand team interactions
+ Provides medical subject matter expertise to promotional material development and other commercial and marketing initiatives
+ Reviews material and projects to ensure scientific alignment and compliance with good promotional practice
+ Signs off for medical review of promotional materials
+ Acts as affiliate signatory on relevant documents where required.
+ Provides medical support to the marketing and product planning groups for new products, line extensions, and new indications.
+ Support launches by engaging external KOLs to gather insights, providing scientific evidence trainings and creating promotional materials with commercial colleagues.
+ Serves as a point of medical query answer provider on queries received from external key stakeholders (e.g. KOLs, doctors, allied healthcare professionals etc.) and internal stakeholders (e.g. other functions QA, RA, PV, commercial team etc.)
+ Creates or modifies slide decks for external stakeholders to use for disease talks during local scientific meetings/discussion forums/formulary submissions.
+ Provides training and refresher course on therapeutic area when requested by internal stakeholders.
+ Conducts medical/marketing activities that increases capabilities of internal sales force (e.g. journal clubs)
+ Leads and facilitates scientific discussion between Abbott staff and external KOLs on Abbott related products and therapeutic areas.
May Serve as Affiliate Safety Representative or "back-up Affiliate Safety Representative"
+ Supports implementation of effective Pharmacovigilance systems operating within the affiliates, and that reporting requirements to competent authorities for adverse events and other safety related documents are adhered to.
+ Proactively anticipates possible safety signals and communicate appropriately according to standard procedures
Lead affiliate and Subregional Clinical Research
+ Initiates discussion/meetings and co-write research protocols with external KOLs on scientific topics of interest to further Abbott products reach to the scientific community.
+ Oversees clinical study activities of the affiliates to ensure compliance with corporate Standard Operating Procedures SOP's, GCP, and local regulatory requirements pertaining to the conduct of clinical studies.
Support Medical Governance
+ Accountable for understanding compliance requirements, risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Medical Affairs Partner, Oncology
Posted 3 days ago
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Job Description
**The Position**
**Position Based in Malaysia**
At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about improving the lives of patients' and are bold in both decision and action. We believe that partnering with health systems around the world can create value for patients, society and for Roche. We are uniquely positioned to realize truly integrated health solutions across pharmaceuticals, diagnostics, digital health and big data solutions; positioning us as a key partner for personalized, sustainable healthcare everywhere.
The Medical Affairs Partner (MAP) demonstrates personal purpose around improving the patient journey, as well as strong passion to create value and impact on the ecosystem. The MAP is a senior level role within the affiliate, who has decision making authority to request resources of Roche (both within the affiliate and broader network) in order to have improved impact on the patient journey.
They are a core member of the disease area pod working in close collaboration with the Patient Journey Partners (PJP). The MAP spends majority of their time in the field close to customers communicating the value of Roche's science and products to physicians, investigators and institutions. They think from an enterprise level, and will also be a member of an APAC level network working across borders, to realize and scale country outcomes by contributing to virtual, cross border, cross functional work package teams.
**The Opportunity:**
The Medical Affairs Partner has a reporting line to the Country Medical, Innovation and Regulatory Lead, serves the affiliate vision with an aligned mindset and behaviors.
+ Oversee the patient journey in its entirety, acts as a system thinker with the ability to identify shared purpose among stakeholders and cocreate with them to bring better outcomes for patients faster by translating insights into strategic and actionable recommendations.
+ Bring the inside out, to bring Roche expertise, science and knowledge to the ecosystem. Steward Roche's products through their lifecycle and supports their appropriate use, which includes sharing their merits with Healthcare Professionals (HCPs) in a truthful and balanced manner. Ensure great experiences whenever stakeholders in the ecosystem engage with Roche employees, products and services.
+ Pull in expertise and resources locally and from the network as needed, prioritize and drive solutions that deliver outcomes faster. Boldly act on key decisions and opportunities and boldly stop any activity that is not adding value.
+ Identify important data gaps and opportunities designing and supporting data generation plans to address them including phase IV studies, registries and real world evidence generation.
+ Hold an altruistic approach in supporting the global network.
+ Act as a leader, coach and mentor, who supports team working and actively contributes to the learning & development of peers across strategically aligned therapy areas, key medical affairs capabilities and engagement with healthcare professionals and patient groups.
+ Display integrity in all levels (i.e. open, honest, ethical and genuine). All Roche employees are expected to practice high standards of compliance with both external and internal policies andregulations as well as participate and be involved in SHE initiatives within the Company.
+ Supports GxP-related activities to ensure quality compliance requirements are adhered to
**Who You Are:**
+ Is self-managed and self-directed, ready to take on empowerment. Demonstrates a growth mindset, able to learn and unlearn quickly, take risks and experiment.
+ Has an enabler mindset leveraging the internal and external networks to create value, sharing back and scaling. Has outstanding partnering capabilities such as coaching, consulting, ability tolisten deeply, question and understand.
+ Willing to travel when needed.
Skills and Experience :
+ Has a deep understanding of patient journey and related treatments, medical affairs strategies & tactics including clinical research as well as broad understanding of Roche's present portfolio andfuture pipeline, such that they can work on future-based solutions. Is able to effectively sharescientific information including investigational findings through direct communications andengagement at scientific conferences with healthcare professionals and/or the scientific community.
+ Has excellent stakeholder engagement skills including partnering with Therapeutic Area Experts (TAEs) and organizations isrequired. Experience partnering with Patient Advocacy Group(PAGs) is highly desired.
+ Evidence generation skills is required. Supports relevant Product Development Medical Affairs (Global Medical Affairs) (PDMA) and Country Clinical Operationstrial, Early Access Program and Compassionate Use program activities within their diseasearea/ecosystem
+ Work efficiently and harmoniously in a cross-functional team, able to formulate cross-functionalstrategies and orchestrate cross-functional teams. Experience in agile ways of working is highlydesired.
+ Experience with medical review of promotional materials is required.
+ Ability to leverage digital means and tools is required.
+ Proficiency in English is required, fluency in the local language is desired.
+ Trained in GMP and GDP requirements for pharmaceutical
Education & Expertise:
+ Medical degree and/or PHD preferred, bachelor's degree in life sciences (eg. immunology,biomedical, biology or pharmacy) required.
+ Minimum of 3 years experience within a Medical Affairs role in Pharmaceutical, Diagnostics,Health Sciences, Biotechnology or other related fields is required.
+ Experience and expertise in **Oncology** , specifically HCC and Lung Cancer is preferred.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
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