17 Experienced Medical Specialist jobs in India

Job Overview
Provide a wide range of medical surveillance support (including monitoring of clinical laboratory data for subjects in clinical studies and composing medical narratives and interfacing with investigator sites.)
Essential Functions
- Monitor, and evaluate laboratory results on a daily basis from sponsor-designated central laboratory
- Evaluating and analyzing laboratory data at agreed frequency from sponsor-designated data management system/eDC platform
- Conduct preliminary review of laboratory results relative to established protocol-specific reference range guidelines, using relevant clinical laboratory experience and compares current results with prior laboratory values to evaluate or note clinically significant increases/decreases and contacts the investigator site for pertinent additional clinical contact for distribution to project team
- Serve as liaison between the Medical Services Department and sponsor-designated laboratory and the IQVIA Project Team
- Maintain up-to-date laboratory knowledge via continuing education activities or attendance at medical seminars
- Based on clinical laboratory and monitoring experience, identify potentially significant trends or shifts in laboratory results and alerts IQVIA Medical Advisors
- Interact with project team to convey critical information that may impact study objectives
- Work with central laboratory staff to facilitate appropriate monitoring and reporting of subject laboratory results
- Assists Lead Medical Surveillance Specialist with project set-up activities
- Attends project team meetings, as needed
- Performs other related duties as assigned
Qualifications
- Bachelor's Degree Life Sciences or allied health sciences,ie pharmacy,biochemistry, microbiology, biotechnology,nursing, biotechnology, medical laboratory sciences, physiotherapy
- health care ie medical (allopathy, homeopathy,ayurveda), or dentistry,
- 2 to 6 years relevant experience with a minimum 2.5 years of medical surveillance experience (req).
- r equivalent combination of education, training and experience.
- Strong technical ability to comprehend and integrate scientific data from a variety of sources. Strong communication
skills, both written and verbal. Demonstrated computer skills, especially word processing and data management. Strong
analytical and organizational skills and attention to detail required.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Job Overview
Provide a wide range of medical surveillance support (including monitoring of clinical laboratory data for subjects in clinical studies and composing medical narratives and interfacing with investigator sites.)
Essential Functions
- Monitor, and evaluate laboratory results on a daily basis from sponsor-designated central laboratory
- Evaluating and analyzing laboratory data at agreed frequency from sponsor-designated data management system/eDC platform
- Conduct preliminary review of laboratory results relative to established protocol-specific reference range guidelines, using relevant clinical laboratory experience and compares current results with prior laboratory values to evaluate or note clinically significant increases/decreases and contacts the investigator site for pertinent additional clinical contact for distribution to project team
- Serve as liaison between the Medical Services Department and sponsor-designated laboratory and the IQVIA Project Team
- Maintain up-to-date laboratory knowledge via continuing education activities or attendance at medical seminars
- Based on clinical laboratory and monitoring experience, identify potentially significant trends or shifts in laboratory results and alerts IQVIA Medical Advisors
- Interact with project team to convey critical information that may impact study objectives
- Work with central laboratory staff to facilitate appropriate monitoring and reporting of subject laboratory results
- Assists Lead Medical Surveillance Specialist with project set-up activities
- Attends project team meetings, as needed
- Performs other related duties as assigned
Qualifications
- Bachelor's Degree Life Sciences or allied health sciences,ie pharmacy,biochemistry, microbiology, biotechnology,nursing, biotechnology, medical laboratory sciences, physiotherapy
- health care ie medical (allopathy, homeopathy,ayurveda), or dentistry,
- 2 to 6 years relevant experience with a minimum 2.5 years of medical surveillance experience (req).
- r equivalent combination of education, training and experience.
- Strong technical ability to comprehend and integrate scientific data from a variety of sources. Strong communication
skills, both written and verbal. Demonstrated computer skills, especially word processing and data management. Strong
analytical and organizational skills and attention to detail required.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Our client, a premier medical spa renowned for its advanced treatments and exceptional client care, is seeking a highly skilled and certified Aesthetician to join their team. This exciting role offers the opportunity to work with cutting-edge technologies and premium skincare products in a luxurious and professional environment. You will be responsible for providing a wide range of aesthetic services, including facials, chemical peels, microdermabrasion, laser treatments, and body contouring. The ideal candidate will possess a deep knowledge of skincare science, a keen eye for detail, and a passion for helping clients achieve their aesthetic goals. Exceptional interpersonal skills and the ability to create a welcoming and relaxing experience for clients are paramount.

Key responsibilities include:

• Performing comprehensive skin analysis and recommending personalized treatment plans.
• Delivering a variety of advanced aesthetic treatments using state-of-the-art equipment.
• Educating clients on proper skincare techniques and product recommendations.
• Maintaining accurate and confidential client records.
• Ensuring a high standard of cleanliness and sanitation in treatment rooms and common areas.
• Staying up-to-date with the latest trends and advancements in the beauty and wellness industry.
• Building and nurturing strong client relationships to encourage repeat business and referrals.
• Assisting with inventory management and restocking of treatment supplies.
• Collaborating with medical professionals to ensure client safety and optimal treatment outcomes.
• Providing exceptional customer service and ensuring client satisfaction at every touchpoint.

This position requires a licensed and certified Aesthetician with a proven track record of delivering high-quality treatments. You should possess excellent communication skills, a professional demeanor, and a passion for the beauty and wellness industry. A strong understanding of anatomy, physiology, and dermatology is beneficial. Our client offers a supportive work environment, ongoing training and development opportunities, and a competitive compensation package. This role is based in Chandigarh and requires flexibility in working hours, including occasional weekends.
Location: Chandigarh, Chandigarh, IN

Our client, a pioneering pharmaceutical company, is seeking an experienced and highly motivated Lead Medical Affairs Specialist to drive strategic medical engagement and scientific communication. This is a fully remote position, offering the flexibility to contribute impactful insights from anywhere. The successful candidate will play a crucial role in developing and executing the medical affairs strategy for key therapeutic areas, fostering relationships with key opinion leaders (KOLs), and ensuring the scientific integrity of our client's products. You will be at the forefront of translating complex scientific data into clear, compelling communications for diverse audiences.

Key Responsibilities:

• Develop and implement comprehensive medical affairs plans aligned with company objectives and product strategies.
• Engage with Key Opinion Leaders (KOLs), healthcare professionals (HCPs), and academic institutions to foster scientific exchange and collaboration.
• Provide scientific and medical input for product development, clinical trials, and post-market surveillance activities.
• Develop and review scientific and educational materials, ensuring accuracy, compliance, and clarity.
• Support the planning and execution of medical education programs, symposia, and advisory boards.
• Analyze and interpret clinical data, generating insights to inform medical strategy and communications.
• Ensure adherence to all relevant regulatory guidelines, ethical standards, and internal policies.
• Collaborate with cross-functional teams, including R&D, Marketing, and Regulatory Affairs, to ensure seamless integration of medical affairs activities.
• Monitor the competitive landscape and emerging scientific trends within relevant therapeutic areas.
• Contribute to the training and development of other medical affairs team members.

Qualifications:

• Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical discipline.
• Minimum of 7 years of experience in medical affairs within the pharmaceutical or biotechnology industry.
• Demonstrated expertise in strategic planning and execution of medical affairs initiatives.
• Proven experience in building and managing relationships with KOLs and HCPs.
• Strong understanding of clinical research, drug development processes, and regulatory requirements.
• Exceptional scientific communication, presentation, and writing skills.
• Ability to critically evaluate scientific literature and data.
• Excellent project management and organizational skills.
• Proficiency in relevant therapeutic areas is highly desirable.
• Self-starter with a proven ability to work independently and effectively in a remote setting.

This is a unique opportunity to shape the medical narrative for innovative therapies from the comfort of your home office. If you are passionate about advancing medical science and possess the requisite expertise, we encourage you to apply for this remote-first role.

Our client, a rapidly expanding pharmaceutical company at the forefront of medical innovation, is seeking a highly experienced Lead Medical Affairs Specialist to join their team in **Bhubaneswar, Odisha, IN**. This on-site role is crucial for bridging the gap between scientific research and clinical application, ensuring that healthcare professionals receive accurate and comprehensive information about the company's products. You will be instrumental in developing medical communication strategies, engaging with key opinion leaders (KOLs), and supporting the medical education initiatives. The ideal candidate possesses a strong scientific background, exceptional communication skills, and a deep understanding of the pharmaceutical landscape.

Responsibilities:

• Develop and execute strategic medical affairs plans in alignment with product development and commercial objectives.
• Serve as a primary scientific and medical resource for assigned therapeutic areas.
• Identify, establish, and maintain relationships with key opinion leaders (KOLs) and other medical experts.
• Develop and deliver high-quality scientific and medical information to healthcare professionals through various channels (e.g., presentations, publications, advisory boards).
• Support the development of medical education materials and programs.
• Review and approve promotional and non-promotional materials for scientific accuracy and compliance.
• Collaborate with cross-functional teams, including R&D, marketing, sales, and regulatory affairs, to ensure cohesive strategies.
• Analyze and interpret clinical data to provide insights and support evidence-based decision-making.
• Contribute to the planning and execution of medical advisory boards and scientific meetings.
• Ensure all activities comply with relevant industry regulations, ethical guidelines, and company policies.

Qualifications:

• Advanced degree (M.S., Ph.D., Pharm.D., M.D.) in a relevant scientific or clinical discipline.
• Minimum of 7 years of experience in medical affairs, clinical research, or a related scientific role within the pharmaceutical industry.
• In-depth knowledge of assigned therapeutic areas and a strong understanding of clinical trial design and interpretation.
• Proven experience in engaging with Key Opinion Leaders (KOLs) and managing relationships with medical experts.
• Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and persuasively.
• Strong understanding of pharmaceutical regulations and compliance requirements.
• Demonstrated ability to work independently and collaboratively within a team environment.
• Strategic thinking and excellent project management skills.
• Ability to travel as needed for scientific meetings and KOL engagement.
• A passion for advancing patient care through scientific exchange.

This role offers a significant opportunity to influence medical strategy and scientific communication within a growing pharmaceutical organization in **Bhubaneswar, Odisha, IN**.

Our client is a leading pharmaceutical company seeking a highly motivated and experienced Lead Medical Affairs Specialist to join their remote team. This role offers an exceptional opportunity to contribute to cutting-edge medical strategies and engage with key opinion leaders (KOLs) in the pharmaceutical domain. As the Lead Medical Affairs Specialist, you will be instrumental in developing and executing comprehensive medical affairs plans, ensuring scientific accuracy, and fostering robust relationships within the medical community. You will provide scientific and medical expertise to internal teams, support clinical research activities, and contribute to the development of medical communication materials.

Key Responsibilities:

• Develop and implement strategic medical affairs plans in alignment with company objectives and therapeutic area strategies.
• Identify, engage, and build strong relationships with key opinion leaders (KOLs) and healthcare professionals.
• Provide scientific and medical support to cross-functional teams, including marketing, sales, and R&D.
• Review and approve promotional and non-promotional materials for scientific accuracy and compliance.
• Support the planning and execution of medical education programs, advisory boards, and scientific meetings.
• Contribute to the development of clinical trial protocols, study reports, and publications.
• Stay abreast of the latest scientific advancements, clinical data, and regulatory requirements in relevant therapeutic areas.
• Analyze market trends and competitive intelligence to inform medical strategies.
• Manage medical affairs budgets and ensure efficient resource allocation.
• Ensure adherence to all relevant ethical, legal, and compliance guidelines.

Qualifications:

• Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant life sciences discipline.
• Minimum of 8 years of experience in Medical Affairs, Clinical Development, or Medical Science Liaison roles within the pharmaceutical industry.
• Demonstrated experience in developing and executing medical affairs strategies.
• Proven ability to build and maintain strong relationships with KOLs and healthcare professionals.
• Excellent understanding of clinical trial design, data interpretation, and scientific communication.
• Strong knowledge of regulatory requirements and compliance guidelines in the pharmaceutical industry.
• Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and effectively.
• Strategic thinking, analytical skills, and strong project management abilities.
• Ability to work independently and collaboratively in a remote, global team environment.
• Experience in (Specify Therapeutic Area, e.g., Oncology, Cardiology, Neurology) is highly preferred.

This role is based in Delhi, Delhi, IN , but is a fully remote position accessible from across India.

Our client, a prestigious medical spa, is seeking a highly skilled and compassionate Remote Aesthetician to join their innovative Beauty & Wellness team. This fully remote position offers a unique opportunity to provide expert skincare consultations and treatment planning remotely, leveraging cutting-edge technology and personalized client care. While the client-facing aspect of the role is remote, a strong understanding of in-person treatments and product knowledge is essential for effective consultation. You will be responsible for conducting thorough skin assessments via virtual consultations, understanding client needs, and recommending personalized treatment plans and product regimens. This includes educating clients on various skincare procedures, ingredients, and at-home care routines to achieve their aesthetic goals. You will maintain detailed client records, track progress, and schedule follow-up virtual appointments. The ideal candidate possesses a deep knowledge of dermatology, advanced skincare techniques, and a wide range of aesthetic treatments. Exceptional communication, empathy, and customer service skills are paramount for building trust and rapport with clients remotely. Proficiency in using virtual consultation platforms and CRM systems is required. You should stay abreast of the latest trends and innovations in the beauty and wellness industry to provide the most effective and up-to-date advice. This role is perfect for a licensed aesthetician looking to expand their reach and impact, offering expert guidance from the convenience of their home office. You will contribute to enhancing client satisfaction and driving product sales through expert remote consultations. A passion for skin health and a commitment to client well-being are essential for success in this specialized remote role.

Key Responsibilities:

• Conduct virtual skincare consultations and assessments.
• Develop personalized treatment plans and product recommendations for clients.
• Educate clients on skincare procedures, ingredients, and at-home care.
• Maintain accurate and detailed client records using virtual platforms.
• Track client progress and schedule follow-up consultations.
• Stay updated on industry trends, new treatments, and skincare technologies.
• Promote and sell skincare products and services effectively.
• Provide exceptional remote customer service and support.
• Collaborate with the medical spa team on client care strategies.
• Ensure a consistent and positive client experience.

Qualifications:

• Licensed Aesthetician with a valid certification.
• Minimum of 3 years of experience in aesthetic skincare treatments and consultations.
• In-depth knowledge of dermatology, skin physiology, and cosmetic ingredients.
• Excellent virtual communication, interpersonal, and client management skills.
• Proficiency with virtual consultation software and CRM systems.
• Understanding of various aesthetic treatments (e.g., facials, peels, laser).
• Strong sales and customer service orientation.
• Ability to work independently and manage time effectively in a remote setting.
• Passion for beauty, wellness, and client education.

About the job
**Our Team:**
_Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally._
**Main responsibilities:**
_The overall purpose and main responsibilities are listed below:_
_Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases. Initiate and amend submission based on comments (as required). Support the writer with internal and external stakeholder communication. Track the delivery of activities (including managing issues and risks) and support follow up. Support required submission, compliance/ approval activities, and ensure compliance with publication processes and end-to-end publication management tools (e.g., iEnvision - previously, Datavision/Matrix) and update as required with approval/compliance tools (e.g., PromoMats, DAM). Support the management of the assigned publication or medical education in line with the agreed budget. Support and manage as required external spend tracking (e.g., approvals, purchase orders, and goods received). Support adherence to associated compliance related activities and approvals (with internal stakeholder taking accountability for compliance). Collaborate effectively with stakeholders: Scientific communication global and/or local teams; and medical content enhancement teams._
· People: (1) Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and product - with an end objective to develop education and communication content as per requirement; (2) Actively lead and develop SBO operations associates; and (3) Ensure new technologies are leveraged
· Performance: (1) Ensure publication/medical education materials (slide decks, abstracts, posters, and manuscripts etc.) are delivered, stored as per agreed timelines and quality; (2) Develop tools, technology, and process to constantly improve quality and productivity
· Process: (1) Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports; (2) Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the medical writing group; and (3) Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards
· Stakeholder: (1) Work closely with scientific communication/medical content enhancement teams to ensure the end-to-end effective project delivery of the designated publication/medical education deliverables
About you
· **Experience** : _3-5 years post qualification experience_
· **Soft skills** : _Stakeholder management; communication skills; and ability to work independently and within a team environment_
+ **Technical skills** : _Project management; Scientific/Medical writing/communications; Pharma experience (including but not limited to therapeutic area/domain knowledge exposure;_ _and/or_ _publication submission)_
+ **Education** : _University degree level (Graduate degree, preferably in science)._ _Additionally, relevant advanced/postgraduate degree in life sciences/pharmacy/similar discipline desirable_
· **Languages** : _Excellent knowledge of English language (spoken and written)_
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Job title** : **_Project Specialist - Project Specialist - Medical Events_**
+ _Hiring Manager:_ **_Project Lead, Sanofi Global Hub_**
+ _Location:_ **_Hyderabad_**
+ _% of travel expected:_ **_Travel required as per business need_**
+ _Job type:_ **_Permanent and Full time_**
**Our Team:**
_Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions_ __ _. Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations_ __ _in Sanofi, globally._
About the job
_Project Specialists oversee and documents the creation and approval of documents required for events within their areas of responsibility within the OneCRM and PromoMat portal. They evaluate the type of event and organise the creation of the events information within the 1CRM portal that are within their scope, such as advisory board, consulting services, symposium, speaker training, scientific education program, stand-alone meeting, hospital-clinical staff meeting, third party sponsorships, etc._
_Project Specialists contribute their experience and knowledge in the form of recommendations to meet Sanofi's purpose and goals, focusing on efficiency while always staying compliant at every level. They manage and communicate with internal and external stakeholders, ensuring consistent company representation at all events._
_The role requires project management and communication capacity, as well as organization skills, in alignment with Sanofi's Play to Win strategy._
**Main responsibilities:**
+ Manage the end to end event in a project mode by notably organizing withing the OneCRM events portal
+ ensure all relevant information and documents are available to create the events within the OneCRM portal
+ regular coordination with stakeholders until event execution and event closure
+ Partner with events business requestor, events engagement team, for ensuring all approvals are available with relevant documents for every type of event
+ Provide guidance and input regarding process improvements
+ Adhere to company policies, particularly those related to transparency and compliance.
+ In charge of OneCRM events portal management, for all types of events within scope
+ Provide hands-on management of all event communication and documentation including attendee registration and data management for events
+ Ensure KPIs and metrics reporting to sustain synergies
+ Mentor and train incoming rotating specialists and create/updates all training guidelines and materials as needed.
+ Maintain agility, stay updated on any CRM and promomat system updates, and participate in any training sessions organized by the local team for new event processes.
**Requirements**
+ A bachelor's degree is required.
+ Fluent in written and spoken English.
+ Direct experience in the pharmaceuticals and life sciences space.
+ Proficient in MS Office and Veeva Vault.
+ 1 to 3 years of event management experience preferred.
**Competencies:**
+ Strong relationship builder, customer-service oriented.
+ Organized and flexible, able to quickly grasp and implement new concepts.
+ Event knowledge.
+ Financial acumen.
+ Ability to collaborate and focus on outcomes & delivery in multicultural environment.
+ Innovative mindset, digital literacy.
+ Able to adapt to changing business priorities.
+ High attention to detail.
+ Accountability and sense of urgency, proactive and able to find flexible solutions on the spot when challenges arise.
**Stakeholder:**
Work closely with stakeholders from various GBUs, Sanofi Global Hub Activity teams & Sanofi Global Hub leadership
Pursue progress, discover extraordinary.
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (