23 Medical Communication jobs in Singapore

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Within Medical Communications, we improve patient health by supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We manage medical information inquiries, document adverse events and product complaints, report product launches, prepare standard responses to inquiries and develop process improvements for customer implementation.

Discover Impactful Work:

Provides technical and medical information, and/or performs intake of adverse events/ product complaints with quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to a level in parallel with the individual’s expertise, experience and training.

A day in the Life:

• Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharmaceutical or device products. Processes fulfillments and provides clinical trial information or after-hours on call support.

• Analyzes caller’s questions to formulate an accurate and concise response using client-approved resources and records inquiries and interactions in the appropriate databases following organizational, client and regulatory guidelines.

• Identifies, records and triages adverse events and product complaints according to organizational, client and regulatory guidelines and provides additional support (including follow up) as needed.

• Maintains thorough knowledge of project and corporate policies and procedures including client products, SOPs, protocols, GCPs, and applicable regulatory requirements.

• Works closely with internal and external client contacts (up to and including members of client management) to resolve complex inquiries. As needed, research medical literature and drafts responses for such inquiries.

Keys to Success:

Education

• Bachelor's degree, health care or life science degree accepted

Experience

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years). Some countries may require a health care professional degree or Medical information experience.

• In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

• Excellent English and Mandarin verbal and written communication skills

• Excellent English and Mandarin language skills (comprehension, speaking, reading and writing); Fluency skills in a second language may be required

• Proficient computer and keyboarding skills

• Good interpersonal skills

• Ability to work independently as well as part of a team.

• Ability to interpret client provided complex medical and technical information

• Organizational and time management skills

• Ability to maintain a positive and professional demeanor in challenging circumstances

Working Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

• Able to work upright and stationary for typical working hours.

• Ability to use and learn standard office equipment and technology with proficiency.

• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

• This position is a hybrid position

• Training will be 12 weeks on site followed by once per week in office expectations

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/DisabilityAccess

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.

• This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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Medical Information Specialist I - Mandarin and English Bilingual

Join to apply for the Medical Information Specialist I - Mandarin and English Bilingual role at Thermo Fisher Scientific

Medical Information Specialist I - Mandarin and English Bilingual

2 days ago Be among the first 25 applicants

Join to apply for the Medical Information Specialist I - Mandarin and English Bilingual role at Thermo Fisher Scientific

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Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Within Medical Communications, we improve patient health by supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We manage medical information inquiries, document adverse events and product complaints, report product launches, prepare standard responses to inquiries and develop process improvements for customer implementation.

Discover Impactful Work:

Provides technical and medical information, and/or performs intake of adverse events/ product complaints with quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to a level in parallel with the individual’s expertise, experience and training.

A day in the Life:

• Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharmaceutical or device products. Processes fulfillments and provides clinical trial information or after-hours on call support.
• Analyzes caller’s questions to formulate an accurate and concise response using client-approved resources and records inquiries and interactions in the appropriate databases following organizational, client and regulatory guidelines.
• Identifies, records and triages adverse events and product complaints according to organizational, client and regulatory guidelines and provides additional support (including follow up) as needed.
• Maintains thorough knowledge of project and corporate policies and procedures including client products, SOPs, protocols, GCPs, and applicable regulatory requirements.
• Works closely with internal and external client contacts (up to and including members of client management) to resolve complex inquiries. As needed, research medical literature and drafts responses for such inquiries.
  
  

Keys to Success:

Education

• Bachelor's degree, health care or life science degree accepted
  
  

Experience

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years). Some countries may require a health care professional degree or Medical information experience.
• In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
  
  

Knowledge, Skills, Abilities

• Excellent English and Mandarin verbal and written communication skills
• Excellent English and Mandarin language skills (comprehension, speaking, reading and writing); Fluency skills in a second language may be required
• Proficient computer and keyboarding skills
• Good interpersonal skills
• Ability to work independently as well as part of a team.
• Ability to interpret client provided complex medical and technical information
• Organizational and time management skills
• Ability to maintain a positive and professional demeanor in challenging circumstances
  
  

Working Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary for typical working hours.
• Ability to use and learn standard office equipment and technology with proficiency.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
• This position is a hybrid position
• Training will be 12 weeks on site followed by once per week in office expectations
  
  

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/DisabilityAccess

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.

• This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
  
  

Seniority level

• Seniority level Not Applicable

Employment type

• Employment type Full-time

Job function

• Job function Training, Consulting, and Customer Service
• Industries Pharmaceutical Manufacturing and Biotechnology Research

Referrals increase your chances of interviewing at Thermo Fisher Scientific by 2x

Sign in to set job alerts for “Medical Information Specialist” roles. Executive, Medical Affairs Office (2-year contract) Senior Executive, Medical and Scientific Affairs Assistant Manager / Senior Assistant Manager, Medical Affairs Clinical Governance Head of Medical Affairs - Asia Pacific (Including GCA) Clinical Safety Coordinator - Pharmacovigilance / Drug Safety Regional Product & Medical Affairs Lead - Asia Pacific Research Assistant (Core Support Faculty - O&G)

Queenstown, Central Singapore Community Development Council, Singapore 6 days ago

Associate Regulatory Affairs / Quality Assurance Manager (Medical Device / Up to 9K)

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**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Within Medical Communications, we improve patient health by supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We manage medical information inquiries, document adverse events and product complaints, report product launches, prepare standard responses to inquiries and develop process improvements for customer implementation.
**Discover Impactful Work:**
Provides technical and medical information, and/or performs intake of adverse events/ product complaints with quality customer service. Analyzes and researches inquiries and documents interactions according to organizational, client and regulatory guidelines. The information provided will be given to a level in parallel with the individual's expertise, experience and training.
**A day in the Life:**
+ Responds accurately and professionally to technical and medical information inquiries received via phone, email, internet or mail in reference to pharmaceutical or device products. Processes fulfillments and provides clinical trial information or after-hours on call support.
+ Analyzes caller's questions to formulate an accurate and concise response using client-approved resources and records inquiries and interactions in the appropriate databases following organizational, client and regulatory guidelines.
+ Identifies, records and triages adverse events and product complaints according to organizational, client and regulatory guidelines and provides additional support (including follow up) as needed.
+ Maintains thorough knowledge of project and corporate policies and procedures including client products, SOPs, protocols, GCPs, and applicable regulatory requirements.
+ Works closely with internal and external client contacts (up to and including members of client management) to resolve complex inquiries. As needed, research medical literature and drafts responses for such inquiries.
**Keys to Success:**
**Education**
+ Bachelor's degree, health care or life science degree accepted
**Experience**
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years). Some countries may require a health care professional degree or Medical information experience.
+ In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills, Abilities**
+ Excellent **English and Mandarin verbal and written communication skills**
+ Excellent **English and Mandarin language skills** (comprehension, speaking, reading and writing); Fluency skills in a second language may be required
+ Proficient computer and keyboarding skills
+ Good interpersonal skills
+ Ability to work independently as well as part of a team.
+ Ability to interpret client provided complex medical and technical information
+ Organizational and time management skills
+ Ability to maintain a positive and professional demeanor in challenging circumstances
**Working Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary for typical working hours.
+ Ability to use and learn standard office equipment and technology with proficiency.
+ Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
+ This position is a hybrid position
+ **Training will be 12 weeks on site followed by once per week in office expectations**
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility/DisabilityAccess
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1- *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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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)

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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.

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.

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Job Title ">

Administrative Support for Medical Affairs

We are seeking a highly organized and detail-oriented administrative professional to support our Medical Affairs team.

The successful candidate will provide administrative support for Clinical Fellow hiring, document verification, medical affairs promotion-related tasks, manpower billing processes, and documentation and record keeping of doctors' Manpower Service Agreements (MSA).

Key Responsibilities:

• Provide administrative support for Clinical Fellow hiring administration
• Verify documents for Clinical Fellow applicants
• Support medical affairs promotion-related tasks
• Manage manpower billing processes
• Document and record keep doctors' Manpower Service Agreements (MSA)

Requirements:

• Min Diploma/Bachelor in any field
• No experience required as training provided

What We Offer:

Competitive compensation package

Opportunity to work with a dynamic team

Professional development and growth opportunities

Flexible working hours

Collaborative work environment

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.

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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