146 Medical Affairs jobs in Singapore

Primary Job Function:
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.
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About Lucence
Lucence is advancing cancer care through precision oncology, delivering clinically actionable insights through next-generation sequencing (NGS) and liquid biopsy technology. Our work spans treatment selection, minimal residual disease (MRD), and multi-cancer early detection (MCED).
About the Role
The Medical Affairs personnel will play a pivotal role in shaping and executing Lucence’s medical strategy, with a focus on precision oncology solutions spanning MRD, MCED, and therapy selection. This role will build and maintain strong scientific partnerships with oncologists, hematologists, and pathologists while driving evidence generation and contributing to clinical development programs. Preference will be given to candidates with molecular diagnostics or precision oncology experience, as this broad skillset enables cross-functional contributions beyond a traditional pharma background.
Key Responsibilities
Build and sustain high-quality scientific relationships with key opinion leaders (KOLs), including oncologists, hematologists, and pathologists.
Provide in-depth clinical and scientific education on Lucence’s precision oncology portfolio, covering MRD, MCED, and therapy selection applications.
Lead and support regional KOL engagement initiatives, advisory boards, and educational programs.
Actively contribute to evidence generation and clinical development strategies, leveraging skills across Medical Affairs, real-world data, and investigator-led research.
Collaborate cross-functionally with Medical, Clinical, Commercial, and Product teams to shape business and medical strategy.
Gather, analyze, and communicate actionable field insights and emerging scientific trends to internal stakeholders.
Represent Lucence at scientific conferences and professional society meetings, and support clinical study initiatives.
Contribute to the design and execution of evidence generation studies, including real-world data programs similar our LIQUIK study.
Ensure seamless channel integration between Sales, Marketing, Medical Affairs, Evidence, and Clinical Development functions.
Qualifications
MD, PhD, or PharmD strongly preferred in oncology, molecular biology, genetics, or a related field
Minimum 2 years’ experience in Medical Affairs, or a clinical/scientific role in oncology or diagnostics
Expertise in NGS, liquid biopsy, and the clinical application of molecular testing
Familiarity with MRD and MCED technologies and their clinical adoption
Skilled at presenting complex data to HCPs and cross-functional teams
Knowledge of Singapore and APAC healthcare systems, with ability to support U.S. engagements
Strong communication, collaboration, and relationship-building skills
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JOB DESCRIPTION
Provide clinical expertise in clinical evaluation, and literature search and appraisal technical documentation according to MDR 2017/745 and MEDDEV guidelines.
Provide clinical expertise in post-market clinical follow-up (PMCF) and post-market surveillance (PMS) technical documentation including the creation and update of the Summary of Safety and Clinical Performance (SSCP) according to MDR 2017/745 and MDCG guidelines.
Provide safety and clinical assessment of complaints and adverse events including technical write-up of the manufacturer’s incident report (MIR).
Create, review and update procedures, work instructions, protocols and reports related to clinical evaluation, literature search and appraisal, post-market clinical follow-up (PMCF), post-market surveillance (PMS) and Summary of Safety and Clinical Performance (SSCP) according to current standards and guidance, and periodic schedule.
Participate in the risk management team and provide safety and clinical assessment in the risk management file (RMF) on identified risks from different data sources during post-production processes that is in accordance with the requirements of ISO 14971.
Provide support in the MDR documentation, application, submission and review as and when needed by the superior.
Provide support in the creation, update and maintenance of the technical files according to MDR 2017/745 requirements.
Perform market research and analysis on clinical trials and product outlook from different online sources.
Provide support on the internal audits and external certification audits in compliance with ISO 13485, other applicable standards and regulations.
Plan, develop and implement clinical strategies in accordance with applicable guidance, standards and regulations.
Interface with Bioptimal’s contracted manufacturer on the clinical needs of the company and the strategies to obtain compliance to applicable guidance, standards and regulations.
Act as Singapore representative in communicating the clinical needs to different stakeholders and obtaining approval on clinical evaluations.
Take lead in the creation, update, execution, follow-up and compiling of clinical surveys according to procedure.
REQUIREMENTS
Degree in medical or in life science with at least 5 years professional work experience in invasive catheter or cardiology related medical devices’ clinical evaluation, with PhD is an added advantage.
Working knowledge on regulatory requirements relating to clinical evaluation is a must, with MDR 2017/745 background is an added advantage.
Preferably with good research methodology (including clinical investigation design and biostatistics).
Must be scientific and data-driven with good information management (experience with relevant databases such as Embase, Medline, PubMed, etc.)
Fluent and experienced in technical writing related to clinical evaluation and literature search and appraisal.
Fluent in both verbal and written English.
With high level of integrity and able to work on tight deadlines and deliver results as per schedules.
Self-starter, independent, analytical thinker and able to recommend sound, logical advice to management in accordance with applicable regulations and guidance.
With good interpersonal and communication skills, positive outlook and able to get along with peers.
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Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.
La 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 and regulations 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 to listen 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 and future pipeline, such that they can work on future-based solutions. Is able to effectively share scientific information including investigational findings through direct communications and engagement 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 is required. 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 Operations trial, Early Access Program and Compassionate Use program activities within their disease area/ecosystem
Work efficiently and harmoniously in a cross-functional team, able to formulate cross-functional strategies and orchestrate cross-functional teams. Experience in agile ways of working is highly desired.
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 Ophthalmology, specifically retinal diseases such as Neovascular Age-related Macular Degeneration (nAMD) and Diabetic Macular Edema (DME) is preferred. Open to those with other TA experiences as well.
Qui nous sommes
Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.
Construisons ensemble un avenir plus sain.
Roche est un employeur offrant l'équité en matière d'emploi.
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Job Responsibilities:

• Provide administrative support for residency program activities and events

• Execute resident onboarding operations, including administration of training agreements, setting up IT and clinical access, and preparation of staff IDs, name tags and other essential items

• Maintain accurate and up-to-date resident records, including rotation schedules, leave of absence applications, and resident movements

• Maintain records of faculty, resident development, scholarly activities, CME attendance, training time and duty hours

• Process and track NHG Personal Training Fund applications

• Compile reports on peer review learning and training milestone

• Administer conference application for doctors including conference leave and claims applications

• Attend to enquiries from stakeholders about resident deployment, ensuring clarity and accuracy

Job Requirements:

• Diploma in any discipline with at least 2 years of relevant experience

• Experience in healthcare or educational institutions will be an advantage

• Proficient in Microsoft Office, particularly Excel

• Excellent organisational, coordination, and time-management skills

• Excellent interpersonal and communication abilities, both verbal and written

Please do not apply to this job posting. Interested candidate, please apply through NSC Career Portal at

Job Responsibilities:

• Work closely with Clinical Services, Clinical Heads, other staff members of Clinical Services, internal and external stakeholders.
• Liaise with MOH and other ministry statutory boards on all hospital licensing and inspection matters.
• Coordinate and conduct Internal Hospital Quality Audit and support Quality Assurance and Clinical Services Committees.
• Provide secretariat support for Patient Record Review Committee meetings.
• Conduct audit on medical case notes to ascertain the level of completeness of clinical documentation.
• Manage Hospital Dashboard Clinical Data base (Balance score Card/ Quality Indicators).
• Ensure and maintain the roster for "Doctors On-Call" in a timely and regular manner.
• Provide oversight on document control matters, work with internal stakeholders to coordinate/work on the development or update Clinical Services' SOPs in the hospital.
• Provide administrative and secretariat support (drafting meeting minutes) for various committees and ensure proper documentation of all meetings and follow-up.

Job Requirements:

• Experience in related areas (e.g. healthcare, clinical operations, finance) would be an advantage.
• Diploma or degree holder.
• Strong team player in a fast-pace environment with good interpersonal and communication skills (verbal and written).
• Keen eye for details.
• Adaptable, able to multi-task, work well independently and eager to learn.

Overview
You will be part of a team to
provide administrative and clerical support
in the Medical Affairs team. This includes requesting case notes and assigning requests to doctors, managing various reports and correspondences relating to patient care, coordinating posting-in and posting-out of House Officers. You will also assist in other projects assigned to you.
Responsibilities
Provide administrative and clerical support in the Medical Affairs team; request case notes and assign requests to doctors; manage reports and correspondences relating to patient care; coordinate posting-in and posting-out of House Officers; assist in other projects as assigned.
Qualifications
Diploma holders or GCE 'O' / ’A’ Level or its equivalent with at least 3 years' relevant experience. Those with healthcare administrative experience will be an advantage.
Strong interpersonal skills with a good command of verbal and written English
Meticulous with good organisation and co-ordination skills
Able to work independently
Proficient in Microsoft Office applications
Only shortlisted candidates will be notified.
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Job Responsibilities:

• Work closely with Clinical Services, Clinical Heads, other staff members of Clinical Services, internal and external stakeholders.
• Liaise with MOH and other ministry statutory boards on all hospital licensing and inspection matters.
• Coordinate and conduct Internal Hospital Quality Audit and support Quality Assurance and Clinical Services Committees.
• Provide secretariat support for Patient Record Review Committee meetings.
• Conduct audit on medical case notes to ascertain the level of completeness of clinical documentation.
• Manage Hospital Dashboard Clinical Data base (Balance score Card/ Quality Indicators).
• Ensure and maintain the roster for “Doctors On-Call” in a timely and regular manner.
• Provide oversight on document control matters, work with internal stakeholders to coordinate/work on the development or update Clinical Services’ SOPs in the hospital.
• Provide administrative and secretariat support (drafting meeting minutes) for various committees and ensure proper documentation of all meetings and follow-up.

Job Requirements:

• Experience in related areas (e.g. healthcare, clinical operations, finance) would be an advantage.
• Diploma or degree holder.
• Strong team player in a fast-pace environment with good interpersonal and communication skills (verbal and written).
• Keen eye for details.
• Adaptable, able to multi-task, work well independently and eager to learn.