17 Medical Consulting jobs in Malaysia

• Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, 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 respective 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 stakeholder 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 teams, 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.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt. Distribution of marketing samples (where applicable)
  
  

• Medical Doctor, PHD or Degree in Pharmacy
• English Clinical Research Phases; Medical Science and Disease Area Knowledge; Medical Education and Scientific Engagement; Third-Party Sponsored Trials Medical Governance
• Able to understand changing dynamics of Pharmaceutical industry
• Proficient and fluent in English (spoken and written), with good interpersonal and communication skills.
• Digital & Technology Savvy
  
  

Job Description Summary

Job Description

Major accountabilities:

• Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, 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 respective 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 stakeholder 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 teams, 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.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt. Distribution of marketing samples (where applicable)

Minimum requirements

• Medical Doctor, PHD or Degree in Pharmacy
• English Clinical Research Phases; Medical Science and Disease Area Knowledge; Medical Education and Scientific Engagement; Third-Party Sponsored Trials Medical Governance
• Able to understand changing dynamics of Pharmaceutical industry
• Proficient and fluent in English (spoken and written), with good interpersonal and communication skills.
• Digital & Technology Savvy

Skills Desired

• To Join a Pharma MNC with great product pipelines
• Chance to represent well-renowned brands portfolios and products

About Our Client

Our client is a global MNC operates within the pharmaceutical industry and is dedicated to delivering innovative healthcare solutions. It is known for its robust pipeline of products and its commitment to improving patient outcomes globally.

Job Description

• Provide scientific and medical expertise to support the development and commercialization of products in the eyecare and neuroscience sectors.
• Collaborate with cross-functional teams to develop and implement medical strategies aligned with business goals.
• Act as a scientific liaison with healthcare professionals to communicate relevant clinical data and product information.
• Review and approve promotional and medical materials to ensure compliance with regulatory standards.
• Deliver training sessions to internal teams on therapeutic areas and product information.
• Monitor and analyze market trends to provide insights and recommendations for medical activities.
• Support clinical research initiatives by offering medical expertise and oversight.
• Ensure alignment with ethical and compliance standards in all medical activities.

The Successful Applicant

A successful Medical Advisor - Opthal/Neuroscience should have:

• A degree in medicine, pharmacy, or a related field within the life sciences industry.
• Experience in medical affairs within the pharmaceutical sector is a Must, and good to have strong knowledge in relevant therapeutics areas
• Excellent communication and presentation skills to engage with internal and external stakeholders.
• Ability to analyze and interpret clinical data effectively.
• Familiarity with regulatory and compliance requirements in the industry.
• A proactive approach to problem-solving and delivering results.

What's on Offer

• Competitive fixed salary
• Comprehensive benefits package, including basic pay, performance bonus, and fixed allowances.
• Opportunities to work within an established pharmaceutical company.
• Exposure to innovative products and cutting-edge medical advancements.
• Collaborative and professional working environment in Malaysia.

Job Description - Manager, Medical Advisor & Case Management (25000C9)

Manager, Medical Advisor & Case Management (Job Number: 25000C9 )

About the Job

To provide medical consultation and opinion in regard to claims pertinent to Guarantee
Letter (GL) or Reimbursement / medical claim disputes or appeals / investigations / underwriting, and to ensure effective implementation of case management intervention in order to efficiently reduce or contain healthcare cost, without compromising healthcare quality and needs, in addition to development of quality assurance programmes or other relevant initiatives for organization.

Medical advisory lead within and beyond operations divisions. To provide medical insights to various divisions within the company such as Medical Claims, Network Management, Call Centre, Customer Services, Product Management & Pricing, Strategic Business
Development etc.

• To monitor and follow up with complex cases that require prolonged stay or due for discharge based on the length of stay planned / benchmarked; with the objective of limiting unwarranted extension of stay without compromising the care quality and to evaluate /approve for Top Up GL that fulfills criteria set within the proposed benchmark.
• To provide medical consultation and opinion in regard to admissibility and necessity of medical claims, fulfilment of policy contract definition in medical claims, investigation and underwriting decisions, as well as ad-hoc medical consultation and opinion in medical
  related queries.
• To communicate with panel specialists via call conference or virtual meetings regarding Professional Fee Queries and address overcharging issues or any issues on specialist’s fees to appropriate parties such as hospital management / hospital fee committee and Ministry of Health (MOH), medical councils, LIAM / PIAM as and when required, in accordance with the PHFSA Fee Schedule and reasonable & customary charges (R&C)
  guides.
• To develop / coach claim assessors through regular medical trainings and development / revision of internal claims guidelines in order to enhance their medical knowledge and competency in claim assessment to deliver services in keeping with the standards set.
• To involve in projects and/or initiatives for department / division process improvement.
• To conduct quality assurance checking on medical claims; to vet through periodical service report and follow up with relevant parties for remedial actions and its implementation as and when required.
• As part of the leadership team, work with key stakeholders to proactively shape the organisation’s culture and conduct environment that is aligned to the organization’s Core Values.
• Takes accountability in considering business and regulatory compliance risks and takes appropriate steps to mitigate the risks.
• Maintains awareness of industry trends on regulatory compliance, emerging threats and technologies in order to understand the risk and better safeguard the company’s interest.
• Highlights any potential concerns / risks and proactively shares the best risk management practices.
• In charge of fraud, waste and abuse (FWA) detection, resolution and prevention to minimize billing wastages by reviewing and analyzing trends and emerging patterns in hospital and doctors’ charges, implementing controls on claims overutilization.

• Qualifications: Licensed practicing Medical Doctor (MBBS / MD) in good standing in medical community, preferably with clinical experience / specialty in internal medicine, paediatrics, and surgical based. Postgraduate qualification in occupational health, family medicine, or any relevant field would be an added advantage. Experience in a public / private hospital is essential. Experience in analysis, fraud detection is an added
  advantage.
• Working Experience: Minimum 5 years working experience in healthcare and/or
  insurance.
• Key Skills: Sound medical knowledge; knowledge of healthcare billing and medical terminology; strong business acumen with communication, analytical, problem solving, documentation and organization skills; strong negotiation and public relation skills.
• Key Knowledge: Knowledge in medical terminology, clinical knowledge; Proficiency in current healthcare delivery systems and hospital, patient management and billing system; insurance product and contractual wordings knowledge.
• Key Competencies: Customer service, product knowledge, medical knowledge, information gathering and analysis, policy interpretation and application, processes, procedures and policies.
• Demonstrates alignment with the organisation’s core values through expected behaviours
• High level of integrity, takes accountability of work and good attitude over teamwork.
• Takes initiative to improve current state of circumstances and adaptable to embrace new
  changes.

Who we are

Founded in 1908, Great Eastern is a well-established market leader and trusted brand in Singapore and Malaysia. With over S$100 billion in assets and more than 16 million policyholders, including 12.5 million from government schemes, it provides insurance solutions to customers through three successful distribution channels – a tied agency force, bancassurance, and financial advisory firm Great Eastern Financial Advisers. The Group also operates in Indonesia and Brunei. The Great Eastern Life Assurance Company Limited and Great Eastern General Insurance Limited have been assigned the financial strength and counterparty credit ratings of "AA-" by S&P Global Ratings since 2010, one of the highest among Asian life insurance companies. Great Eastern's asset management subsidiary, Lion Global Investors Limited, is one of the leading asset management companies in Southeast Asia. Great Eastern is a subsidiary of OCBC, the longest established Singapore bank, formed in 1932. It is the second largest financial services group in Southeast Asia by assets and one of the world’s most highly-rated banks, with an Aa1 rating from Moody’s and AA- by both Fitch and S&P. Recognised for its financial strength and stability, OCBC is consistently ranked among the World’s Top 50 Safest Banks by Global Finance and has been named Best Managed Bank in Singapore by The Asian Banker.

To all recruitment agencies: Great Eastern does not accept unsolicited agency resumes. Please do not forward resumes to our email or our employees. We will not be responsible for any fees related to unsolicited resumes.

To All Recruitment Agencies Great Eastern does not accept unsolicited agency resumes. Please do not forward resumes to our email or our employees. We will not be responsible for any fees related to unsolicited resumes.

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 us on social media: Facebook, Instagram, YouTube, LinkedIn, and TikTok.

The Medical Advisor is responsible for office-based and field activities within the therapeutic area, supporting country AMD and in-country medical scientific liaison (MSL) activities, particularly managing Medical and Scientific Information, Medical Affairs content, and supporting commercial activities in Eye Care & Neurosciences in Singapore and Malaysia.

Reporting to the Medical Affairs Country Lead, Malaysia & Singapore, you will provide high-level scientific and clinical support to external and internal customers, establishing and developing relationships with Key Opinion Leaders (KOLs) across the spectrum of products within this therapeutic area and emerging indications.

You will be based in Malaysia, responsible for field-based medical affairs activities, with more than 50% of your time expected to 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 and presentations on clinical and scientific topics, ensuring compliance approval.
• Organize and deliver advisory board meetings with HCPs to stimulate scientific exchange and gather business-relevant information.
• Assist in organizing and scientifically supporting external events such as satellite symposia.
• Organize and participate in external education and training events as appropriate.
• Facilitate development of Investigator Initiated Trials (IIT) Proposals in line with Allergan Strategy.
• Support publication of clinical data in line with Allergan Strategy.
• Support other research activities, such as real-world evidence collection.
• Establish and maintain relationships with KOLs and identify new KOLs in line with Allergan strategy.
• Attend scientific congresses to interact with KOLs and gather wider therapy area and competitor information.
• Collaborate with KOLs in strategic advisory meetings and develop KOL advocacy.
• Maintain knowledge of therapy area, Allergan products, and the competitive landscape.
• Support the business by attending leadership meetings and working cross-functionally.
• Guide on appropriate speakers for congresses and workshops.
• Organize clinical and scientific education and in-house training for sales reps and staff.
• Develop medical affairs plans aligned with SEA cluster commercial plans.
• Contribute to scientific dossiers and reports as appropriate.

Qualifications

• Medical Doctor, Ophthalmologist, Neuroscientist, Biologist, Chemist, or Pharmacist with an MD, PharmD, or PhD degree.
• Experience in pharmaceutical or medical device industry, ideally in scientific medical liaison or medical advisor roles.
• Excellent communication, analytical, and interpersonal skills.
• Experience engaging with opinion leaders and understanding clinical data.
• Ability to communicate scientific data clearly and concisely.
• Strategic thinking, adaptability, and results-oriented mindset.
• Ability to work autonomously and in a team, with strong organizational skills and flexibility to travel.

AbbVie is an equal opportunity employer committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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 onX ,Facebook ,Instagram ,YouTube ,LinkedIn andTik Tok .

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/Botox Therapeutics (Botox indications in neurology) 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.

• 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.

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.

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