medical affairs manager

Zydus Group

<div>
 <p>
  Job Description Position: Manager, Medical Affairs
 </p>
 <p>
  <br/>
 </p>
 <p>
  Roles and Responsibilities:
 </p>
 <p>
  <br/>
 </p>
 <p>
   Devise strategies and planning for launch of new indication/products including KOL engagement and medical education
 </p>
 <p>
   Liaise with professional associations and KOLs to build and drive scientific advocacy for the product/therapy area
 </p>
 <p>
   Drive medical education and scientific dialogue for products and therapy area in collaboration with cross functional teams
 </p>
 <p>
   Excellent interpersonal and communication skills  Collaborate with the marketing department to develop marketing strategies
 </p>
 <p>
   Conduct analysis of products and product pipeline
 </p>
 <p>
   Building a professional rapport with Key Opinion Leaders
 </p>
 <p>
   Support sales force trainings, present science news, activity plans etc.
 </p>
 <p>
   Collaboration with external medical experts
 </p>
 <p>
   Provide refresher training to sales/marketing through ongoing training initiatives.  Provide pre-launch and launch training to sales staff for new products
 </p>
 <p>
   Ability to devise phase 4 post-marketing studies incl. registries, RWE, observational studies  Approval of promotional inputs as per IFPMA guidelines
 </p>
 <p>
   Resolution of scientific queries received from sales/marketing/doctors with sound scientific back-up
 </p>
 <p>
   Ability to present scientific content at academic meets like CMEs, conferences, advisory boards etc.
 </p>
 <p>
   Medical Writing Skills Desired Candidate Profile:
 </p>
 <p>
  <br/>
 </p>
 <p>
   Fresher MD Pharmacology / Medicine
 </p>
 <p>
   MD Pharmacology/Medicine with 2+ years of experience in medico-marketing role will be considered for Sr. Manager role
 </p>
 <p>
   MBBS with 2 years of experience in medico-marketing
 </p>
</div>


Medical Affairs Manager

IPSEN

<div><p><b>The role of the Medical Manager is to:</b></p><ul><li>
Deploy and adapt Ipsen Medical Affairs strategy throughout the Kingdon, including tactics and execution.</li><li>
Manage Scientific Information dissemination and maintaining relationships with key partners.</li><li>
Coordinate and manage all scientific supporting documentation related to IPSEN products and therapeutic areas where the company is involved</li><li>
To coordinate in collaboration with Group Medical department the local performance of clinical trials</li></ul><p><b>
Business Support
</b></p><ul><li>Ensure compliant collaboration with HCPs and HCOs through Ipsen systems and SOPs</li><li>
To manage and mentor MSLs and conduct their performance appraisal for medical affairs and lead medical organisation to deliver effective teamwork</li><li>
Sets medical affairs strategy for the portfolio in cooperation with other departments and aligns the medical strategy with regional strategies and plans</li><li>
To deploy medical affairs team members including MSLs</li><li>
Ensures execution of medical affairs activities in the country with highest standards of quality and compliance</li><li>
Accountable for medical pre-launch, launch, and post-launch preparation and execution</li><li>
Leads the medical scientific communication, medical education and medical expert/KOL interactions</li><li>
Develops and manages long-term relationship with external stakeholders/KOLs</li><li>
Whenever requested, provide expert clinical opinion/information to external and internal customers &ndash; ensures medical product training for Ipsen sales force staff</li><li>
To support Marketing department in the supervise, review, and approval of promotional materials from medical point of view ensuring that all local legal requirements and other applicable (e.g. Ethical codes) as well as those established by the Ipsen Group are met, ensure highest quality of scientific non-promotional materials prepared by medical department as well</li><li>
Integrated cross-functional plans and collaboration with Marketing and Access teams</li><li>
Maintaining a &ldquo;library&rdquo; of relevant articles, presentations provided by experts to IPSEN</li><li>
To participate at brand teams, work and campaigns preparation</li><li>
Participate at preparation of Budget and Strategic plan with focus on medical activities and their budget management</li></ul><p><b>
Clinical Trial and Development</b></p><ul><li>
To facilitate and coordinate the participation of Ipsen in clinical trials developed by IPSEN Group</li><li>
To ensure Ipsen provides trial feasibility evaluation to global team via dedicated medical advisor.</li><li>
To establish, implement, advise and coordinate local clinical study protocols, reports and publications viz. feasibilities.</li><li>
Ensure full support for Pharmacovigilance including compliance with Adverse Event reporting and ensure risk management plan implementation</li><li>
Ensures providing support and consulting advisory to local group of clinical monitors</li><li>
Assist in resolving country specific issues in clinical trial preparation/execution</li><li>
To ensure contact with local HCP regarding international as well as local research projects</li></ul><p><b>
Regulatory and Pharmacovigilance Support
</b></p><ul><li>To ensure that clinical studies, regulatory requirements and medical pharmacovigilance system is provided in compliance with Ipsen SOPs and national regulations for all actual and future Ipsen products</li><li>
To ensure the required medical support to pharmacovigilance responsible person in all matters related to this area</li><li>
On time reports spontaneous adverse events and technical complaints for all Ipsen products</li></ul><p><b>
Competencies</b></p><ul><li><b>
Drive Purpose:</b><ul><li>
Puts values and ethics at the forefront of everything;</li><li>
Anchors Ipsen's purpose, mission and commitments to patients and society.</li></ul></li><li><b>
Drive Vision and Strategy:</b><ul><li>
Paints a compelling picture of the vision (future status quo) and strategy that motivates others to action</li></ul></li><li><b>
Excellence in execution:</b><ul><li>
Approaches priority setting and setting the stage through the lens of execution;</li><li>
Establishes clarity about the goals, accountabilities, timelines, and next steps; can identify/spot opportunities for real impact on patient and society;</li><li>
Able to be focused and performance-driven with clear KPIs</li><li>
Plans and aligns effectively (steps, resources, timelines etc.);</li><li>
Displays a commitment to best practice sharing and setting</li><li>
Promotes single point of accountabilities.</li></ul></li><li><b>
Collaborates</b><ul><li>
Collaborates and communicates without boundaries, continuously removes organizational barriers;</li><li>
Focuses on continuous improvement; integrates and leverages key learnings, showcases resourcefulness, learning/experimenting at scale, demonstrates strong entrepreneurial behaviors and mindset.</li></ul></li><li><b>
Customer (&amp; Patient) focus
</b><ul><li>Displays and echoes the patients' voice through all touchpoints;</li><li>
Understands and integrates the patient ecosystem view;</li><li>
Integrates the patient voice into everything we do;</li><li>
Ensures we set and shape our sight on what matters for patients and society</li></ul></li></ul><p></p><p><b>
Knowledge &amp; Experience (essential):</b></p><ul><li>
Experiences in Medical in a Multinational Pharmaceutical company</li><li>
People Management</li></ul><p><b>
Knowledge &amp; Experience (preferred):</b></p><ul><li>
 Experience with Clinical Trials</li></ul><p><b>
Education / Certifications (essential):</b></p><ul><li>
 MD preferred, or Pharmacist Degree</li></ul><p><b>
Language(s) (essential):</b></p><ul><li>
English</li><li>
Arabic</li></ul></div>

Medical Manager

hirelink

<p><b>Job Title: Sr. Scientific Executive/Asst. Manager &ndash; Scientific/Deputy Manager &ndash; Scientific </b></p><p><b>Qualification</b>: M.Pharm/PharmD in Pharmacology</p><p><b>About Us:</b> We are hiring for a a leading name in the pharmaceutical industry, dedicated to innovation and excellence. We are committed to delivering high-quality products and staying at the forefront of medical research.</p><p>Join our dynamic team and contribute to shaping the future of healthcare.</p><p><b>Role Overview:</b> We are seeking a Sr. Scientific Executive/Asst. Manager &ndash; Scientific/Deputy Manager &ndash; Scientific to join our Medical Affairs team. This role involves driving medical initiatives, supporting product launches, providing scientific support, and engaging with key stakeholders to ensure the delivery of high-quality medical information.</p><ul><li>Product Launch: Conduct comprehensive literature reviews and prepare medical manuals and presentations. Deliver impactful new product launch presentations to the marketing team and field force, including technical insights.</li><li>Query Resolution: Address queries from field representatives and doctors, ensuring strong customer relationships. Provide relevant scientific support to resolve complex queries effectively.</li><li>Scientific Support: Stay updated with the latest scientific developments, therapy area guidelines, and landmark trials. Provide technical support to marketing and sales teams, validating medical content for accuracy. Prepare prescribing information and organize CME kits, including PowerPoint presentations and key references.</li><li>Training: Conduct training sessions for new hires and refresher courses for medical representatives to disseminate medical knowledge effectively.</li><li>New Product Ideation: Provide medical rationale for new product launches and suggest innovative dosage forms, indication expansions, and novel product ideas. Publications: Prepare and publish manuscripts for peer-reviewed journals, including original research and review articles.</li></ul><p><i><b>Desired Candidate Profile: </b></i></p><p><b>Education: M.Pharm in Pharmacology is mandatory. </b> Experience: Minimum 2 years in a relevant role. Freshers may also apply.</p><p><b>Skills: </b>Strong knowledge of medical and scientific concepts. o Excellent communication, presentation, and interpersonal skills. o Proficiency in preparing medical literature, presentations, and publications. Ability to collaborate across teams and maintain customer focus.</p><p><b>Why Join Us? </b></p><p>Opportunity to work with a leading pharmaceutical company.</p><p>Engage in impactful medical affairs activities and product innovations.</p><p>Professional growth through continuous learning and training opportunities.</p><p>Kindly share your resumes on careers@hirelinkpro.com</p><p>Contact: 8197198414</p><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: Up to ₹500,000.00 per year</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Work Location: In person</p>

Medical Affairs/Medico Marketing

ADVANZ PHARMA

<div><div><div><p><b>Date: </b>17 Feb 2026
</p><p><b>Location:</b> Andheri (East), IN, Mumbai 400
</p><p><b>Company: </b>AdvanzPharma
</p><div><div><b>Location: Andheri, Mumbai.</b></div>
<div><b>
(Hybrid working)</b></div><br>
<div></div>
<div><b>
About ADVANZ PHARMA</b></div><br>
<div></div>
<p>
ADVANZ PHARMA is a global pharmaceutical company with the purpose to improve patients&rsquo; lives by providing and enhancing the specialty, hospital, and rare disease medicines they depend on.</p>
<p>
Our ambition is to be a partner of choice for the commercialisation of specialty, hospital, and rare disease medicines in Europe, Canada, and Australia. In line with our ambition, we are partnering with innovative biopharma and pharmaceutical development companies to bring medicines to patients.</p>
<p>
Headquartered in London, UK, we have c700 employees based across more than 20 countries, including key countries in Europe, the US, Canada, and Australia. Our Centre of Excellence in Mumbai, India, as well as an established global distribution and commercialisation partner network complement our global operations.</p>
<p>
ADVANZ PHARMA&rsquo;s product portfolio and pipeline comprises innovative medicines, specialty generics &amp; biosimilars, and originator brands. Our products and pipeline cover a broad range of therapeutic areas, including hepatology, gastroenterology, anti-infectives, critical care, endocrinology, CNS, and, more broadly, rare diseases.</p>
<p>
We can only achieve our ambition with the passion of our dedicated and highly qualified people, acting in line with our company values of entrepreneurship, speed, and integrity.</p><br>
<div></div>
<div><b>
About the Role</b></div>
<div>
The Associate Director, Global Medical Affairs (Biosimilars) is responsible for the development, execution, and continuous optimisation of global medical affairs activities across the ADVANZ PHARMA biosimilar portfolio. The role provides scientific leadership and strategic insight to support successful launches, lifecycle management, and cross-functional decision-making across European, and other global markets.</div><br>
<p></p>
<p><b>
What You&rsquo;ll Do:</b></p>
<p><b>
Medical Strategy, Insights &amp; Lifecycle Leadership</b></p>
<ul>
<li>Review medical insights to provide strategic actions that directly influence launch planning, patient forecasting assumptions, and lifecycle management decisions.</li>
<li>Develop and maintain a deep understanding of patient flows, treatment pathways, and decision drivers across key markets.</li>
<li>Monitor competitor intelligence, including scientific, clinical, and strategic developments, and translate insights into actionable recommendations.</li>
<li>Review relevant scientific literature, synthesising and disseminating key findings to internal stakeholders.</li>
<li>Support and contribute to forecasting guidance, including assumptions linked to clinical positioning, market dynamics, and competitive landscape.</li>
</ul>
<p><b>Development of Medical Resources &amp; Materials</b></p>
<ul>
<li>Development of global medical resources for biosimilars, ensuring scientific accuracy, clarity, and regional relevance.</li>
<li>Develop and maintain medical launch packs to support new product introductions.</li>
<li>Create and implement listening priorities to capture meaningful medical insights from the field.</li>
</ul>
<p><b>Medical Training &amp; Capability Building</b></p>
<ul>
<li>Create medical training decks and supporting materials for internal stakeholders.</li>
</ul><ul><li>Design and deliver medical training programs aligned to global strategy and product lifecycle stage, engaging with external experts as required.</li>
<li>Identify educational needs, and develop additional training materials and tools aligned to medical strategy and launch priorities.</li>
<li>Support capability building across global and regional Medical Affairs teams through structured training initiatives.</li>
</ul>
<p><b>Medical Education &amp; External Engagement</b></p>
<ul>
<li>Assist with the creation and execution of external medical education initiatives, where applicable, ensuring alignment with strategy and compliance requirements.</li>
<li>Provide scientific input into external educational content and ensure consistency across markets.</li>
</ul>
<p><b>Governance, Compliance &amp; Cross-Functional Collaboration</b></p>
<ul>
<li>Manage medical materials review and approval processes, ensuring compliance with internal SOPs and external regulations.</li>
<li>Review regulatory dossiers and provide medical input when required.</li>
<li>Act as a key medical partner to Commercial, Market Access, Regulatory, and Pharmacovigilance teams.</li>
</ul>
<p><b>Other responsibilities</b></p>
<ul>
<li>Manage project budget within given product(s)/therapy area.</li>
<li>Ensure all activities are undertaken with due regard to ADVANZ PHARMA compliance requirements and relevant rules/regulations.</li>
<li>Other tasks, as directed by the supervisor, or based on a specific appointment, or determined during the annual objectives setting process, or by relevant key performance indicators.</li></ul><br>
<p></p>
<div><b>
About You</b></div>
<div>
We are looking for highly motivated individuals who are passionate about making a meaningful difference to patients&rsquo; lives.</div><br>
<div>
</div><div>For this role, you will also have the following:</div>
<div><b>
Qualifications:</b>
</div><ul><li>Medical Doctor (MD) required</li></ul><br>
<div></div>
<div><b>
Knowledge, Skills &amp; Experience:</b></div>
<ul>
<li>Significant experience in Medical Affairs in the pharmaceutical or biotechnology industries with proven experience across global, European, and/or Asian markets.</li>
<li>Strong background in Biosimilars or speciality generics.</li>
<li>Therapy area experience in rheumatology, gastroenterology or haematology preferred</li>
<li>High digital and AI aptitude, with experience leveraging innovative tools to enhance Medical Affairs effectiveness</li>
<li>Demonstrated experience in product launches, lifecycle management and working with commercialisation in non-European markets</li>
</ul><ul><li>Must be an excellent leader and mentor.</li>
<li>Scientifically curious and intellectually rigorous, with a strong drive to stay at the forefront of biosimilar and therapeutic area developments</li>
<li>Clear and compelling communicator, able to translate complex scientific data into meaningful insights for diverse audiences</li>
<li>Highly collaborative, thriving in cross-functional and cross-regional teams and valuing diverse perspectives.</li>
<li>Inspired by our values of entrepreneurship, speed, and integrity.</li>
<li>Sets ambitious goals and high standards for the team.</li>
<li>Persists &ndash; does not give up despite barriers and obstacles.</li>
<li>Strong work ethic and desire to win.</li></ul><br>
<div></div>
<div><b>
Why ADVANZ PHARMA?</b></div><br>
<div></div>
<div>
The success of any company is driven by its people, and we are no different.</div><br>
<div></div>
<div>
At ADVANZ PHARMA, we believe in empowering our people to be entrepreneurs and embrace challenges to enable personal and company growth in an agile and fast-paced environment. We strive to do that inclusively and responsibly, treating all employees with integrity whilst rewarding outcomes and impact.</div><br>
<div></div>
<div>
Our teams are made up of people from all walks of life and backgrounds. We thrive in an environment where uniqueness is celebrated, but we are all united by the same passion to help improve patients' lives by providing and enhancing the specialty and hospital medicines they depend on.</div><br>
<div></div>
<div>
As a business, we like to tap into new ideas and fresh perspectives. So, if you join us, you&rsquo;ll be empowered to own your work, explore new possibilities, and make things happen.</div><br>
<div></div>
<div>
But there&rsquo;s more to you &ndash; and us &ndash; than just work, which is why our culture, vision, and values are so high on our agenda. We believe in gender equality and actively encourage women into senior roles &ndash; we have an active ADVANZ PHARMA Women&rsquo;s Network; almost 40% of our managers are women.</div><br>
<div></div>
<div>
We work hard to recognise and reward talent, and we actively promote from within - last year, approximately 25% of our people across the company achieved promotions. In addition, we recognise talent with our annual Impact Awards, in which our top performers are rewarded for their hard work and dedication.</div><br>
<div></div>
<div>
We offer flexible, agile working options, and you will also enjoy a highly competitive salary and benefits package.</div><br>
<div></div>
<div>
To join us on our exciting journey, apply now! *</div><br>
<div></div>
<ul><li>Please include a CV and Cover letter.</li></ul></div></div></div></div><p></p>

Associate Director, Global Medical Affairs (Biosimilars)

<p></p><div><p><b>The role of the Medical Manager is to:
</b></p><ul><li>Deploy and adapt Ipsen Medical Affairs strategy throughout the Kingdon, including tactics and execution.
</li><li>Manage Scientific Information dissemination and maintaining relationships with key partners.
</li><li>Coordinate and manage all scientific supporting documentation related to IPSEN products and therapeutic areas where the company is involved
</li><li>To coordinate in collaboration with Group Medical department the local performance of clinical trials
</li></ul><p><b>Business Support
</b></p><ul><li>Ensure compliant collaboration with HCPs and HCOs through Ipsen systems and SOPs
</li><li>To manage and mentor MSLs and conduct their performance appraisal for medical affairs and lead medical organisation to deliver effective teamwork
</li><li>Sets medical affairs strategy for the portfolio in cooperation with other departments and aligns the medical strategy with regional strategies and plans
</li><li>To deploy medical affairs team members including MSLs
</li><li>Ensures execution of medical affairs activities in the country with highest standards of quality and compliance
</li><li>Accountable for medical pre-launch, launch, and post-launch preparation and execution
</li><li>Leads the medical scientific communication, medical education and medical expert/KOL interactions
</li><li>Develops and manages long-term relationship with external stakeholders/KOLs
</li><li>Whenever requested, provide expert clinical opinion/information to external and internal customers &ndash; ensures medical product training for Ipsen sales force staff
</li><li>To support Marketing department in the supervise, review, and approval of promotional materials from medical point of view ensuring that all local legal requirements and other applicable (e.g. Ethical codes) as well as those established by the Ipsen Group are met, ensure highest quality of scientific non-promotional materials prepared by medical department as well
</li><li>Integrated cross-functional plans and collaboration with Marketing and Access teams
</li><li>Maintaining a &ldquo;library&rdquo; of relevant articles, presentations provided by experts to IPSEN
</li><li>To participate at brand teams, work and campaigns preparation
</li><li>Participate at preparation of Budget and Strategic plan with focus on medical activities and their budget management
</li></ul><p><b>Clinical Trial and Development
</b></p><ul><li>To facilitate and coordinate the participation of Ipsen in clinical trials developed by IPSEN Group
</li><li>To ensure Ipsen provides trial feasibility evaluation to global team via dedicated medical advisor.
</li><li>To establish, implement, advise and coordinate local clinical study protocols, reports and publications viz. feasibilities.
</li><li>Ensure full support for Pharmacovigilance including compliance with Adverse Event reporting and ensure risk management plan implementation
</li><li>Ensures providing support and consulting advisory to local group of clinical monitors
</li><li>Assist in resolving country specific issues in clinical trial preparation/execution
</li><li>To ensure contact with local HCP regarding international as well as local research projects
</li></ul><p><b>Regulatory and Pharmacovigilance Support
</b></p><ul><li>To ensure that clinical studies, regulatory requirements and medical pharmacovigilance system is provided in compliance with Ipsen SOPs and national regulations for all actual and future Ipsen products
</li><li>To ensure the required medical support to pharmacovigilance responsible person in all matters related to this area
</li><li>On time reports spontaneous adverse events and technical complaints for all Ipsen products
</li></ul><p><b>Competencies
</b></p><ul><li><b>Drive Purpose:
</b><ul><li>Puts values and ethics at the forefront of everything;
</li><li>Anchors Ipsen's purpose, mission and commitments to patients and society.
</li></ul></li><li><b>Drive Vision and Strategy:
</b><ul><li>Paints a compelling picture of the vision (future status quo) and strategy that motivates others to action
</li></ul></li><li><b>Excellence in execution:
</b><ul><li>Approaches priority setting and setting the stage through the lens of execution;
</li><li>Establishes clarity about the goals, accountabilities, timelines, and next steps; can identify/spot opportunities for real impact on patient and society;
</li><li>Able to be focused and performance-driven with clear KPIs
</li><li>Plans and aligns effectively (steps, resources, timelines etc.);
</li><li>Displays a commitment to best practice sharing and setting
</li><li>Promotes single point of accountabilities.
</li></ul></li><li><b>Collaborates
</b><ul><li>Collaborates and communicates without boundaries, continuously removes organizational barriers;
</li><li>Focuses on continuous improvement; integrates and leverages key learnings, showcases resourcefulness, learning/experimenting at scale, demonstrates strong entrepreneurial behaviors and mindset.
</li></ul></li><li><b>Customer (&amp; Patient) focus
</b><ul><li>Displays and echoes the &quot;patients' voice&quot; through all touchpoints;
</li><li>Understands and integrates the patient ecosystem view;
</li><li>Integrates the patient voice into everything we do;
</li><li>Ensures we set and shape our &quot;sight&quot; on what matters for patients and society
</li></ul></li></ul><p></p><p><b>Knowledge &amp; Experience (essential):
</b></p><ul><li>Experiences in Medical in a Multinational Pharmaceutical company
</li><li>People Management
</li></ul><p><b>Knowledge &amp; Experience (preferred):
 </b></p><ul><li>Experience with Clinical Trials
</li></ul><p><b>Education / Certifications (essential):
 </b></p><ul><li>MD preferred, or Pharmacist Degree
</li></ul><p><b>Language(s) (essential):
</b></p><ul><li>English
</li><li>Arabic
</li></ul><p></p>We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace &ldquo;The Real Us&rdquo;. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.</div>

EAZYMED TECHNOLOGIES PRIVATE LIMITED

<p>Role: Manager - Medical Affairs &amp; Programs</p><p><b>Location: Bengaluru</b></p><p>About MrMed</p><p>MrMed is redefining access to life‑saving super‑speciality medicines in India. We&rsquo;re building the country&rsquo;s most trusted digital pharmacy for complex therapies, making treatments more accessible, affordable, and reliable for patients across every corner of India.</p><p>By combining technology, logistics, and medical expertise, we simplify everything from medicine access to patient education with empathy and precision. Our mission is simple: to bridge the gap between speciality care and those who need it most.</p><p>The Opportunity</p><p>We&rsquo;re looking for a doctor who&rsquo;s ready to move beyond clinical practice and shape the next chapter of healthcare delivery in India.</p><p>As Manager - Medical Affairs &amp; Programs, you&rsquo;ll sit at the intersection of medicine, technology, and business, bringing clinical depth to strategic decisions while helping us scale new programs that improve patient outcomes.</p><p>This is a role for someone who wants to build, lead, and influence, not just execute.</p><p>What You&rsquo;ll Lead</p><ul><li><b>Medical Content &amp; Education:</b> Design and review accurate, credible medical content and learning modules for patients, doctors, and partners.</li><li><b>Compliance &amp; Governance:</b> Own the medical compliance process for medicines and patient services; ensure all initiatives meet the highest clinical and ethical standards.</li><li><b>Consultation Programs:</b> Help architect the operations and workflows for virtual doctor consultations, setting up best practices and ensuring compliance.</li><li><b>Cross-Functional Impact:</b> Collaborate with marketing, operations, and product teams to bring medical insight into brand narratives, processes, and decisions.</li></ul><p>What You&rsquo;ll Bring</p><ul><li>MBBS (mandatory); higher qualifications in pharmacology, healthcare management, or digital health are a plus.</li><li>Strong interest in healthcare systems, strategy, or business operations.</li><li>Excellent communication and storytelling skills, written and verbal.</li><li>Detail-oriented, structured thinker with execution bias.</li><li>Entrepreneurial mindset and genuine curiosity about how healthcare businesses scale.</li></ul><p>Why MrMed</p><ul><li>Shape how India accesses and experiences specialty medicines.</li><li>Work with a passionate team that blends medicine, tech, and empathy.</li><li>Build a career path that combines clinical expertise with strategic execution.</li><li>Be part of a fast-growing startup at the frontier of healthcare innovation.</li></ul><p>If you&rsquo;re a doctor ready to rewrite how medicine meets business, this is your stage.</p><p>Apply now and help us build the future of specialty healthcare.</p><p>Share your resume to hr@mrmed.in</p><p>Job Types: Full-time, Permanent</p><p>Pay: ₹35,000.00 - ₹40,000.00 per month</p><p>Benefits:</p><ul><li>Health insurance</li><li>Provident Fund</li></ul><p>Application Question(s):</p><ul><li>Have you completed MBBS</li></ul><p>Work Location: In person</p>

Hiring MBBS Doctor - fresher for the - Medical Affairs & Programs

Gilead Sciences

<div><div>At Gilead, we&rsquo;re creating a healthier world for all people. For more than 35 years, we&rsquo;ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer &ndash; working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world&rsquo;s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.</div><div><br>
Every member of Gilead&rsquo;s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we&rsquo;re looking for the next wave of passionate and ambitious people ready to make a direct impact.</div><div><br>
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.<br>
<br>
Job Description</div><div><br>
We have an exciting opportunity within our Medical Affairs team based in Saudi Arabia for Kite Middle East Medical Lead.</div><div>
The Middle East Medical Lead (Asso. Director /Director- dependent on experience) will have overall responsibility for building and overseeing the strategies and tactics for Cell Therapy within the Kite Middle East Medical Affairs Department, providing strategic leadership for all Medical Affairs activities and developing and executing Medical Affairs strategic initiatives in the Middle East. This position will report to the Kite International Region Head of Medical Affairs.</div><div></div><div>
Everyone at Kite is grounded by one common goal &ndash; curing cancer. We are at the forefront of immunotherapy and engineered T cell therapy. Our personalized approach is what sets us apart. Unlike traditional pharmaceutical manufacturing, our therapies are not created on an assembly line. With CAR T-cell therapy, we are reengineering a patient&rsquo;s own immune cells to fight cancer &mdash; one patient at a time. We also are entering a pivotal time in our history with multiple planned launches and evolving competitive dynamics on a global scale. That means a fast moving, constantly changing environment and innovative culture, where we make discoveries every day &ndash; discoveries that include our own capabilities and our individual potential.</div><div>
Specific Job Requirements:</div><ul><li>
Provides local medical expertise input into global product development for Kite.</li><li>
Represents the company to groups of experts, medical professional groups, societies, regulatory groups at international scientific meetings and national scientific meetings.</li><li>
Develops and leads plans with national/Middle East region cooperative groups to define what are the gaps and potential specific national requirements/needs. Supports the development of local complex clinical data through clinical trials and investigator studies. Supports the development of Health Economic Outcome Research programs for the country.</li><li>
Contributes to the development of the Market access strategy in coordination with the Market Access, Regulatory affairs, Business Unit Director; deliver the medical part of the plan</li><li>
Manage the Middle East Medical Affairs function</li><li>
Develop and execute Medical pre-launch and post-launch Medical plan</li><li>
Medical Budget oversight/control (+/-5% spent)</li><li>
Provides Medical strategic direction and vision and works as a team with the Business Unit Director and Market Access Director.</li><li>
Be part of the International region Medical Affairs Leadership Team and contribute to the overall International region strategy and efforts.</li><li>
Data generation project where applicable</li><li>
Regular communication with external medical community to remain abreast of issues in the field and to provide medical support and direction to them.</li><li>
Engage in peer to peer scientific exchange of complex clinical and scientific information</li><li>
Develop and foster strong scientific relationships with Thought Leaders (TLs), disease experts, and other health care providers (HCPs)</li><li>
Provide clinical/scientific presentations to internal and external groups</li><li>
Compliantly provide internal teams with feedback and insights from interactions and discussions with HCPs<br>
Engage in accrual enhancement activities with clinical trial sites</li><li>
Provide support at professional meetings, including staffing exhibits, reporting on scientific sessions, and facilitating meetings with TLs and HCPs</li><li>
Adhere to corporate and health care compliance guidance in all activities, including those related to clinical trials, scientific interactions with internal and external groups, and responses to unsolicited requests for medical/scientific information</li><li>
Maintain clinical, scientific, and technical expertise in hematology/oncology and the company&rsquo;s therapeutic areas of interest</li><li>
Establish and maintain ongoing long-term collaborative relationships with HCPs (including physicians, nurses, and other allied health professionals) within assigned territory</li><li>
Respond to and document unsolicited requests for scientific information</li><li>
Provide clinical input and training to internal functions as requested</li><li>
Provide support for content development and delivery of clinical presentations at Advisory Boards, as requested</li><li>
Work closely with other field-based employees and headquarters-based staff to rapidly respond to questions from sites</li><li>
Attends most major conferences and helps coordinate Medical Affairs activities at conferences and may present to external audience</li><li>
Responsible for the development and execution of projects that will provide more extensive background, additional data or answers to questions in response to issues that arise relative to commercial, scientific or data needs.</li><li>
Performs medical review at Promotional Review Committees.</li><li>
Manages projects to completion, anticipating obstacles and difficulties that may arise, resolving them in a collaborative manner.</li></ul><div>
Knowledge, Experience and Skills:</div><ul><li>
The ideal candidate will have an advanced degree (e.g. MD, PharmD, PhD, etc.) with significant clinical and research experience in the key therapeutic areas.</li><li>
Industry experience is essential with proven Medical Affairs experiences (7+ years), ideally including recent experience of a successful launch within oncology or hematology.</li><li>
CAR-T therapy experience will be an advantage</li><li>
Must have demonstrated organizational skills to manage multiple projects simultaneously.</li><li>
Must demonstrate strong written and verbal communication skills along with excellent judgment and ability to work in a team environment.</li><li>
Strong presentation skills are required.</li><li>
Prior supervisory/leadership experience.</li><li>
Ability to travel to domestic and international conferences which will include occasional weekend travel is required.</li><li>
Language: Fluent in Arabic and professional level English</li></ul><div></div><div><br>
For Current Gilead Employees and Contractors:</div><div>
Please apply via the Internal Career Opportunities portal in Workday.</div></div>

Medical Affairs Lead - Middle East - Kite

Search 10000+ Medical affairs manager jobs near you this March. New roles added regularly across leading industries. Apply today.

10000 medical affairs manager jobs Near Me

Medical Affairs Manager

Medical Manager

Medical Affairs/Medico Marketing

Associate Director, Global Medical Affairs (Biosimilars)

Medical Manager

Hiring MBBS Doctor - fresher for the - Medical Affairs & Programs

Medical Affairs Lead - Middle East - Kite