296 Medical Communications jobs in Singapore

Get AI-powered advice on this job and more exclusive features.

Direct message the job poster from Gene Solutions

Gene Solutions is a leading company in Vietnam specializing in the research, development and application of the most advanced genetic tests, providing genetic testing services for screening, diagnosis and treatment orientation.

We believe everyone deserves better healthcare via genetic testing. We unlock the power of genetics to transform the healthcare system for a healthier life, by making genetic testing more accessible and helpful than ever. We provide the most comprehensive and innovative solutions at the most competitive price so that everyone can access easily.

We would like to invite you to join us to strengthen and fulfill together this greater purpose.

We are seeking a dedicated Medical Affairs Specialist to join our team. The Medical Affairs Specialist will play a crucial role in supporting the medical and scientific activities related to our gene testing products in the Oncology. This individual will collaborate closely with internal teams, healthcare professionals, and key stakeholders to ensure the effective communication of scientific data and medical education initiatives.

RESPONSIBILITIES:

• Provide medical and scientific expertise on gene testing products in Oncology to internal teams and external stakeholders.
• Develop and review medical materials, including scientific presentations, educational materials, and publications.
• Support the planning and execution of medical education programs, advisory boards, and scientific symposia.
• Collaborate with cross-functional teams to generate and disseminate clinical evidence, including study protocols, data analyses, and publications.
• Serve as a liaison between the company and healthcare professionals, academic institutions, and key opinion leaders in Oncology
• Stay abreast of scientific literature, clinical guidelines, and competitive landscape in the relevant therapeutic area.

REQUIREMENTS:

• Medical degree (MD, MBBS, or equivalent) with specialization in Oncology, or related field.
• Previous experience in medical affairs, clinical research, or healthcare consulting within the pharmaceutical or biotechnology industry.
• Strong understanding of genetic testing, molecular diagnostics, and their applications in Oncology.
• Excellent communication and presentation skills, with the ability to effectively communicate complex scientific concepts to diverse audiences.
• Proven ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.
• Demonstrated leadership skills and strategic thinking in medical affairs activities.
• Ability to travel domestically and internationally as needed.

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Research
• Industries Hospitals and Health Care

Referrals increase your chances of interviewing at Gene Solutions by 2x

Get notified about new Medical Affairs Specialist jobs in Singapore, Singapore .

Clinical Safety Coordinator - Pharmacovigilance / Drug Safety Quality Assurance / Regulatory Affairs Specialist (Medical Devices) Executive, Medical Affairs Office (2-year contract) Assistant Manager / Senior Assistant Manager, Medical Affairs Clinical Governance Associate Clinical Research Coordinator / Clinical Research Coordinator Research Associate, Centre for Population Health Research and Implementation (Contract) Associate Regulatory Affairs / Quality Assurance Manager (Medical Device / Up to 9K) Health Science Study Sponsorship Award - Pharmaceutical Sciences Research Associate (Clinical Healthy Longevity Trials)

Queenstown, Central Singapore Community Development Council, Singapore 3 months ago

Senior / Lead Clinical Research Coordinator, Clinical Trials & Research Unit (2-year contract)

Queenstown, Central Singapore Community Development Council, Singapore 1 month ago

Queenstown, Central Singapore Community Development Council, Singapore 4 months ago

Queenstown, Central Singapore Community Development Council, Singapore 2 months ago

Outram, Central Singapore Community Development Council, Singapore 2 hours ago

Research Assistant (Executive/ Senior Executive),(1 year contract) Research Assistant/Associate (Human Potential TRP)

Queenstown, Central Singapore Community Development Council, Singapore 2 months ago

Head of Medical Affairs - Asia Pacific (Including GCA)

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

#J-18808-Ljbffr

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.

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.

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.

We believe in the power of diversity and inclusion, and strive to identify and create opportunities that enable all people to bring their unique selves to Roche.

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.

#J-18808-Ljbffr

Purpose

The role aims to ensure the effective, reliable, and current communication of GSK's scientific data through external engagements, assisting healthcare professionals and public health decision-makers in delivering appropriate healthcare solutions to patients. Additionally, it involves providing medical and technical expertise to the medical affairs team, brand team, and other internal partners such as regulatory, strategic development, and marketing.

Key Responsibilities

This role will provide YOU the opportunity to lead key activities as follows:

• Support and enable GSK to achieve its business objectives by delivering ‘in-the-field’ scientific engagement with healthcare professionals and public health decision makers to provide scientific and medical information, identify and manage scientific projects and clinical trial activities, compliantly in line with GSK standard operating procedures and local codes of practice, guidelines and laws

• Gain valuable insight and feedback from the healthcare community on GSK products and services, medical and scientific information which can help guide research, development and service provision to benefit GSK’s customers and patients as well as supporting internal stakeholders

• Responsible of development of Medical Strategic Plan/s, execute Scientific Engagement activities and lead external (customer facing) medical projects for assigned portfolio

• Support Medical Governance (compliance to GSK Code, SAPI Code, and other relevant guidelines) in the assigned portfolio of products and contribute to risk review and management monitoring activities

• Provide medical and technical expertise to scientific submissions, and to marketing & sales in the production, review and approval of promotional materials and activities. Final sign off on allocated promotional materials

• Develop an effective communication network and working relationships with relevant global GSK functions.

• Manage the priorities and workloads.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Degree in Medicine, PharmD or PhD in pharmacy

• Min 6 years of Pharmaceutical or Biotech industry experience (medical affairs, clinical development, or medical research)

• Min 2 years’ experience in hepatology or liver-related disease therapeutic area

• Experience interpreting and communicating scientific data and statistics

• Clear understanding of clinical research methodologies and a demonstrated ability to translate scientific, clinical and safety research studies in an effective credible manner. Able to independently evaluate the literature regarding scientific research

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Ability to maintain a command of a large amount of scientific information across multiple products and decide regarding clinical evidence of importance

• Can understand scientific methods and experimental designs

• Ability to work autonomously and independently with time management skills to effectively manage field-based responsibilities.

At Medison, we bring hope to patients living with rare and severe diseases by accelerating access to groundbreaking therapies across global markets. Through strategic partnerships with emerging biotech innovators, we deliver highly novel treatments to patients - no matter where they are in the world.

As the pioneer and leader in global pharmaceutical partnerships, we don’t follow industry standards - we set them. Our mission is to be Always Ahead—in science, in action, and in impact. Every step we take is grounded in our unwavering commitment to improving lives.

We are now looking for a passionate and driven Medical Affairs Manager (MAM) to join our team.

Responsibilities

The role:

This is more than a job - it's a purpose. As MAM, you'll be a key voice of science and strategy on the ground, the scientific face of our organization - building strong, trust-based relationships with healthcare professionals, key opinion leaders (KOLs), and cross-functional partners. You’ll work at the intersection of innovation and patient care, partnering closely with commercial teams, healthcare professionals (HCPs), and key opinion leaders (KOLs) to bring life-changing therapies to patients in need.

You'll play a pivotal role in:

• Engage & Educate : Build collaborative, science-driven relationships with KOLs, medical experts, and HCPs across Singapore.
• Communicate Science : Translate complex data into meaningful insights and deliver impactful presentations to medical audiences.
• Shape Strategy : Shaping and executing the medical engagement and launch excellence strategy.
• Support Early Access : Contribute to local early access initiatives that address urgent unmet needs.
• Deliver Excellence : Drive implementation of medical education initiatives, advisory boards, symposia, and data generation activities.
• Stay Ahead : Monitor competitive intelligence and therapeutic trends to inform market-shaping strategies.
• Build Knowledge : Train internal teams and external partners to strengthen scientific literacy and product understanding.

Requirements

Who You Are

You're a scientifically grounded, patient-centric medical expert with a passion for innovation and rare diseases. You thrive in fast-paced, collaborative environments and are energized by meaningful work that pushes boundaries.

Your background includes:

• Medical or advanced scientific degree (MD, PharmD, PhD preferred)
• 3+ years in pharmaceutical/biotech Medical Affairs in Singapore.
• Strong understanding of theSingapore healthcare system, rare diseases a strong plus.
• Demonstrated experience withproduct launches, scientific exchange, and cross-functional collaboration.
• A strategic mindset with the ability to turn insights into action.
• Proven ability to communicate complex science with clarity and confidence to a variety of audiences.
• Curious, agile, and proactive, with strong initiative and ability to work independently.

Your strengths:

• A natural communicator, educator, and relationship-builder.
• Agile, analytical, and always curious.
• Highly collaborative, with a strong sense of ownership and integrity.
• Digitally savvy and comfortable working in dynamic, cross-functional environments.
• Willing to travel locally to engage with external stakeholders.

Why Join Us?

At Medison, you won’t just work in medical affairs - you’ll redefine what’s possible. You’ll be empowered to shape the future of medicine, improve patient outcomes, and grow your career in a company that values courage, creativity, and care.

Join us and become part of a bold, mission-driven team that’s changing lives - one breakthrough at a time.

#J-18808-Ljbffr

At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal?Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity?Learn more at Function:**
Medical Affairs Group
**Job Sub** **Function:**
Medical Affairs
**Job Category:**
People Leader
**All Job Posting Locations:**
Singapore, Singapore
**Job Description:**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at Head of Medical Affairs SEA & India is tasked with setting the vision for Medical Affairs in the cluster, driving strategic initiatives, and ensuring alignment with global standards. This leadership role involves overseeing the Medical Affairs team and activities across SEA & India, fostering seamless communication and collaboration between local Operating Companies, the Asia Pacific region, and global organizations. The ultimate goal is to support the company's scientific, medical, and commercial objectives through effective management of medical strategies and initiatives within the cluster.
**Responsibilities:**
**Leading SEA & India Medical Strategy**
+ Responsible for leading Country MAF Heads and coordinating input from them on country MAF plans to develop and champion the SEA & India medical strategy and vision across sectors in full lifecycle management and encompassing pre-marketing activities.
+ Responsible for validating medical strategy with key SEA & India KOLs, and building strong ties and partnerships with them
+ Responsible for ensuring alignment of local, regional and Global Medical Affairs strategy, plans and activities within each TA or Sector.
+ Responsible for providing input to AP regional medical strategy to ensure SEA & India requirements are represented.
+ Responsible for ensuring the cascade of relevant information (e.g. Global and AP plans and strategies) through local Medical Affairs Lead/Directors.
+ Accountable for developing and maintaining annual Medical Affairs budget requests and ensuring that individual product budgets are managed and tracked.
+ Close collaboration with SEA & India commercial lead and active participation in SEA & India commercial team meetings to ensure alignment and drive future regional development plans.
**Medical affairs leadership in AP Medical Affairs Meetings**
+ Regional medical affairs leadership role in planning and implementation of patient access programs
**Medical Education**
+ To work with the Portfolio Lead to develop SEA & India Medical Education Plans in line with respective product strategy.
+ Provide a comprehensive Training Plan for internal stakeholders.
+ Review and approve educational and sales materials for medical and scientific accuracy
**Team Leadership**
+ Responsible for coaching and supporting the SEA & India MAF team and the country medical affairs teams in developing and executing their MAF Plans.
+ Responsible for identifying and managing the integration points across the MAF Teams and with other functions and geographies to ensure alignment, minimize risk and eliminate duplication (e.g. coordination of SEA & India studies, interactions with external customers and stakeholders).
+ Review inputs from the local MAF teams to other SEA & India functions such as Regulatory Affairs (RA), Pharmacovigilance / Benefit Risk Management (PV/BRM) etc.
+ Act as a role model with respect to adherence to, and tracking compliance with, relevant Standard Operating Procedures (SOPs), and ensure similar adherence among direct reports.
+ Accountable for effective budget and resource management (headcount, travel, activities, etc.) and managing priorities as appropriate
**Internal & External Network/ KOL Management**
+ Develop KOL management strategy and plan in collaboration with LOCs, facilitating the allocation of responsibility for managing specific KOL relationships along clearly defined lines.
+ Provide MAF oversight and support for market development activities (e.g. SEA & India KOL development strategies, communications plans).
+ Responsible for engaging and influencing top tier KOLs within SEA & India.
+ Develop a SEA & India regional network across Medical Affairs, Regulatory, BRM and Marketing functions to ensure unified SEA & India voice
**Study Planning and Execution**
+ Work with the country MAF and GCDO/MAO teams to ensure that data generation activities are in alignment with medical strategy:
+ Give guidance on the development of study concepts and scientific content for protocols.
+ Accountable for approving study concepts according to defined timelines.
+ Accountable for the final approval of study protocols, ensuring that all comments have been incorporated.
+ Work with the country MAF teams to ensure that Clinical Studies are published and in accordance with the regional and global publication strategy
**Product Safety and Regulatory Requirements**
+ Work with the local countries MAF Lead/Directors to manage Product-related medical safety issues and provide input to the regional compliance person.
+ Support the countries and work with Regulatory Affairs to coordinate and manage Product-related Issues and support major quality incidents/recalls throughout SEA & India
**Requirements:**
+ Academic background with a Medical Degree and/or PhD essential and higher Medical Qualification desirable.
+ At least 10 years industry/business experience with a minimum of 7 years' experience in a relevant area for this function (e.g. Medical Affairs or Clinical R&D, academic or hospitals)
+ In-depth knowledge of study methodology, data review, and analysis.
+ Excellent knowledge of study publication processes.
+ Good knowledge of study execution, benefit risk management and regulatory affairs.
+ Very strong and demonstrable communication and influencing skills that can impact at regional & global level
+ Highly innovative with the ability to drive a complex and changing environment and effectively manage and resolve issues within the SEA & India
+ Experience in managing culturally diverse teams across a region
+ Exceptional leadership, people management and development skills, motivated to develop, guide and reward high performance teams
+ Highly customer and marketplace focused with an awareness of the importance of business results
+ Awareness of and adherence to Johnson & Johnson Credo values

Medical Affairs Executive (Clinical Diagnostic) #HVW

Duties

• Working within a team to ensure clinical confidence in our laboratory diagnostics products by providing medical utility guidance for changes or improvements to existing products as well as during the exploration and development of new and innovative products, in the context of clinical acceptance and applications of standard care and state-of-the-art clinical use.
• Providing medical guidance within and across functional teams to support medical and scientific evidence generation and dissemination, medical communications, technical development activities relating to innovative products or innovative applications of products, regulatory submissions, risk management, and clinical trial planning.
• Develop and implement strategic goals and objectives.
• Conduct surveys to gain valuable insights from clinical trials.
• Providing medical assessments and medical customer support to global product support teams regarding product safety and effectiveness as part of post-commercialization activities.
• Serving as a consultant to help ensure medical messaging is truthful, non-misleading, clear, validated, and aligned with the organization’s strategic positioning.

Requirements

• Min Degree in Pharmaceutical Science/Medicine/Internal Medicine.
• 1-3 years of relevant experience will be advantageous.
• Team player with excellent analytical skills.
• Able to work in a fast-paced environment.

If you are interested in this position, please send your most updated resume to .

Thank you.

Victoria Yam Wen Ting
R21103142
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599

#J-18808-Ljbffr

At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal?Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity?Learn more at Function:**
Medical Affairs Group
**Job Sub** **Function:**
Medical Affairs
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
Singapore, Singapore
**Job Description:**
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Ready to join a team that's pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
The Senior Manager, Medical Affairs - International is a field-based member of the Office of Medical Affairs (OMA) team located in APAC. This role will support the development of professional relationships with Key Opinion Leaders (KOL) in the therapeutic areas of Shockwave Medical (SWAV) and will provide regional scientific support for OMA and International commercial functions. This position will facilitate the timely execution of international studies within the Shockwave Medical (SWAV) investigator-sponsored research (ISR) program, ultimately leading to peer-reviewed evidence dissemination in support of the SWAV strategic evidence plan. This position will also be responsible for supporting major scientific conference activities, including SWAV-sponsored symposia and scientific advisory boards, and will serve as a scientific/Medical Affairs resource to internal regional business partners (Clinical Affairs, Regulatory, Professional Education, Marketing, and Market Access).
**Responsibilities**
+ Support in development of professional and credible relationships with clinical and scientific thought leaders.
+ Interact with KOLs to ensure the execution of international studies within the ISR program in accordance with applicable regulations and SWAV procedures. Serve as point of contact for regional KOLs to facilitate ISR proposal submissions and research contract execution of approved studies. Conduct timely communications with KOLs and internal stakeholders to monitor enrollment and milestone progression of approved ISR studies.
+ Provide appropriate clinical and scientific information for Shockwave Medical products and therapeutic areas in response to unsolicited requests for information.
+ Attend relevant scientific meetings and conferences in support of SWAV conference activities representing OMA as the subject matter expert and point of contact for scientific information.
+ Support in driving communication and education of internal (e.g. commercial, management) and external (e.g. customers, collaborators, distributors) stakeholder on scientific evidence (out of congresses, adboards, funded/sponsored trials)
+ Support the International/European Office of Medical Affairs team with scientific expertise when needed
+ Be a therapeutic expert and provide scientific support for key regional but also International business partners (Clinical Affairs, Regulatory, Marketing, Professional Education and Market Access).
+ Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform SWAV strategic priorities and initiatives.
+ Participate in periodic review of clinical reports, abstracts, manuscripts, and other materials related to scientific data and information.
+ Supporting global OMA functions cross-functionally with scientific expertise for e.g. carotids, TAVI, PAD, CAD or coronary physiology
+ Support Professional Education colleagues in the development and execution of scientific symposia and advisory boards.
+ Support as a representative of the director if necessary.
+ Ensure that all activities and interactions are conducted with due regard to all applicable local and national laws, regulations, guidelines, codes of conduct, company policies and accepted standards of best practice.
+ Other duties as assigned.
Requirements
+ Bachelor's Degree in a scientific field of study. Advance degree strongly preferred (Master, PhD, MD, PharmD, etc.).
+ 7+ years of related experience in Medical Affairs in the medical device industries.
+ Proficient in English (verbal and written) and at least proficiency in an additional Asian language (e.g. Korean, Chinese, or others).
+ Medical device industry experience in cardiovascular medicine with special expertise in carotids, TAVI, PAD, CAD and/or coronary physiology highly preferred.
+ Knowledge of international regulations and guidelines including, but not limited to, medical product communications and response to unsolicited requests off-label information.
+ Ability to understand, summarize, and convey scientific data in a clear and concise manner.
+ Ability to develop and maintain key opinion leader relationships.
+ Works effectively independently and on cross-functional teams.
+ Effective written, verbal and presentation skills across various audiences.
+ Operate as a team or independently while maintaining flexibility and resilience.
+ Proficient in Microsoft Office (Word, Excel, PowerPoint, Teams, Outlook) software.
+ High attention to detail and accuracy, excellent critical thinking skills.
+ Good prioritization and organizational skills.
+ Entrepreneurial "hands-on" experience. Pro-active and a "can do" attitude.
+ Flexible, with a strong ability to work in a fast-paced environment while managing multiple priorities.
+ Ability to travel up to 50% of the time depending on business need.

Roles & Responsibilities

Job Duties

• Ensure complaints are managed expeditiously to enhance overall efficiency and improve overall patient experience.
• Provide sound recommendations to internal stakeholders and addressing patient's feedback confidently to achieve an amicable resolution.
• Establish regular communication channels to ensure all involved parties are informed throughout the investigation process.
• Ensure that the information gathered is comprehensive, relevant, and accurate, minimizing the need for rework.
• Ensure the administrative work and co-ordination of Family Conference between stakeholders and patients are well-managed.
• Ensure projects assigned are executed on time, on target and with quality.

Requirements

• Bachelor's degree
• Excellent interpersonal and communication skills.
• Possess good writing and analytical skills.
• Ability to work collaboratively across all levels or stakeholders.
• Ability to crystallise issues and identify root causes to facilitate effective resolution strategies.
• Ability to maintain composure and clarity of thought under difficult situations.
• Experience in using Microsoft Office is an added advantage.

Interested candidate please click "APPLY" to begin your job search journey and submit your CV directly through the official PERSOLKELLY job application platform - GO Mobile.

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

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its local and overseas subsidiaries and affiliates to collect, use and disclose your personal data to prospective employers/companies based in any country for purposes of evaluating suitability for employment, conducting reference checks, administering employment related services, complying with Government's health advisories and such other purposes stated in our privacy policy. Our full privacy policy is available at If you wish to withdraw your consent, please drop us an ) to let us know. Please feel free to contact us if you have any queries

PERSOLKELLY Singapore Pte Ltd
• RCB No. 20007268E
• EA License No. 01C4394
• Reg No: R1440784 (Foo May Cheng)

Tell employers what skills you have

Microsoft PowerPoint
Microsoft Office
Analytical Skills
Customer Service Delivery
Administrative Work
Customer Service Desk
Interpersonal Skills
Investigation
Administration
Office Administration
Writing
Communication Skills
Administrative Support
Team Player
Microsoft Word
Customer Service
Job Search
Able To Work Independently

Job Duties

• Ensure complaints are managed expeditiously to enhance overall efficiency and improve overall patient experience.
• Provide sound recommendations to internal stakeholders and addressing patient’s feedback confidently to achieve an amicable resolution.
• Establish regular communication channels to ensure all involved parties are informed throughout the investigation process.
• Ensure that the information gathered is comprehensive, relevant, and accurate, minimizing the need for rework.
• Ensure the administrative work and co-ordination of Family Conference between stakeholders and patients are well-managed.
• Ensure projects assigned are executed on time, on target and with quality.

Requirements

• Bachelor’s degree
• Excellent interpersonal and communication skills.
• Possess good writing and analytical skills.
• Ability to work collaboratively across all levels or stakeholders.
• Ability to crystallise issues and identify root causes to facilitate effective resolution strategies.
• Ability to maintain composure and clarity of thought under difficult situations.
• Experience in using Microsoft Office is an added advantage.

Interested candidate please click "APPLY" to begin your job search journey and submit your CV directly through the official PERSOLKELLY job application platform - GO Mobile.

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

By sending us your personal data and curriculum vitae (CV), you are deemed to consent to PERSOLKELLY Singapore Pte Ltd and its local and overseas subsidiaries and affiliates to collect, use and disclose your personal data to prospective employers/companies based in any country for purposes of evaluating suitability for employment, conducting reference checks, administering employment related services, complying with Government’s health advisories and such other purposes stated in our privacy policy. Our full privacy policy is available at . If you wish to withdraw your consent, please drop us an ) to let us know. Please feel free to contact us if you have any queries

PERSOLKELLY Singapore Pte Ltd • RCB No. 20007268E • EA License No. 01C4394• Reg No: R1440784 (Foo May Cheng)