38 Head Of Medical Affairs jobs in Singapore

Location

Singapore, Singapore

Salary

Job Type

Full-time

Date Posted

July 2nd, 2025

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

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.

You may send your resume in PDF to hr-.comindicating your current and expected salary.

We regret that only shortlisted candidates will be notified.

REFERRAL REWARD: SGD$500

• 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.
• Ensure seamless channel integration between Sales, Marketing, Medical Affairs, Evidence, and Clinical Development functions.

• 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

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.

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.
#J-18808-Ljbffr

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
#J-18808-Ljbffr

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.
#J-18808-Ljbffr

• Reputable Organization
• Great Career Opportunity
• Competitive Remuneration Package

As a Assistant Manager/ Senior Assistant Manager, Medical Affairs - Clinical Governance you will be responsible for the following duties:

• Coordinate and support the implementation of clinical quality and safety programmes across the organisation.
• Collaborate with relevant departments to develop quality models, set standards, and design and implement audits and risk management initiatives.

• Provide secretariat and operational support to Quality Assurance and Clinical Services committees, while identifying opportunities to enhance processes and highlight areas for improvement.

• Manage incidents and serious reportable events, including conducting root cause analyses to identify systemic gaps and recommend corrective actions.

• Work closely with stakeholders across departments and institutions to drive change, embed best practices, and foster a culture of continuous improvement.

• Collect, analyse, and interpret quality and safety data to support evidence-based decision-making.

• Develop reports, presentations, and dashboards to track metrics, highlight trends, and recommend improvement strategies.

• Draft and prepare accurate meeting minutes and related documentation.

• Maintain and update the institute's website and other communication platforms to ensure timely and accurate dissemination of quality and safety initiatives.
• Partner with clinicians, administrators, and patients to strengthen awareness, collaboration, and adoption of quality and safety practices.

Requirements:

• Bachelor's Degree
• Experience in related areas (e.g. healthcare services) would be advantageous

To apply, simply click on the ''apply'' button in the job advertisement or alternatively, you can send in your resume via email.

Email Address:.COM.SG

We regret to inform that only shortlisted candidates will be notified.

ALLIED SEARCH PTE. LTD.

EA LICENSE : 19C9777

Family Group: Administration

Job duties & 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 for residents.
• 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