medical affairs manager

Panacea Biotec

<div>
 
 
 Experience: 5&ndash;7 years for Manager
 
 
 
 
 Qualification: MBBS / MD (Pharmacology, Pediatrics, Medicine) OR M.Pharm / PhD (Pharmacology, Life Sciences)
 
 
 
 
 
 
 
 Role Overview
 
 
 
 At Panacea Biotec, the Medical Affairs professional plays a pivotal role in ensuring that our Pharma, Vaccines, and Nutrition portfolios are supported with strong scientific credibility and regulatory compliance. This role involves training the sales force, engaging with healthcare professionals (HCPs), driving scientific communication, and supporting evidence generation to build trust and expand market presence across therapeutic categories, including pediatrics, maternal care, and preventive healthcare.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 1. Medical Expertise &amp; Internal Support
 
 
 <ul>
 <li>
 Deliver structured medical training for the sales force across Pharma, Vaccines, and Nutrition divisions (including new launches).
 </li>
 <li>
 Act as a scientific advisor to marketing, regulatory, and sales teams.
 </li>
 <li>
 Develop and update scientific content repositories (FAQs, objection handlers, scientific briefs).
 </li>
 <li>
 Monitor emerging guidelines, WHO/ICMR/DCGI updates, and competitor data to guide business strategy.
 </li>
 </ul>
 
 
 
 
 
 
 2. Healthcare Professional &amp; KOL Engagement
 
 
 <ul>
 <li>
 Identify, develop, and manage relationships with pediatricians, gynecologists, nutritionists, and infectious disease specialists.
 </li>
 <li>
 Organize advisory boards, CME programs, and medical symposia to establish scientific leadership.
 </li>
 <li>
 Collect and synthesize KOL insights to inform launch strategy and product positioning.
 </li>
 </ul>
 
 
 3. Scientific Communication &amp; Compliance
 
 
 <ul>
 <li>
 Review and approve visual aids, promotional material, detailing decks, and digital campaigns to ensure compliance and scientific accuracy.
 </li>
 <li>
 Support doctor detailing by developing robust scientific narratives for brands like NikoMom and Panacea vaccines.
 </li>
 <li>
 Represent Panacea Biotec at conferences, academic meetings, and pediatric/nutrition forums.
 </li>
 <li>
 Ensure adherence to ethical and regulatory frameworks (DCGI, ICMR, IFPMA, WHO).
 </li>
 </ul>
 
 
 4. Evidence Generation &amp; Clinical Support
 
 
 <ul>
 <li>
 Support investigator-initiated trials, post-marketing surveillance, and real-world evidence (RWE) studies.
 </li>
 <li>
 Collaborate with Pharmacovigilance for safety monitoring and risk management.
 </li>
 </ul>
 
 
 5. Cross-Functional Collaboration
 
 
 <ul>
 <li>
 Partner with Marketing, Sales, Regulatory Affairs, and Market Access to drive scientifically aligned strategies.
 </li>
 <li>
 Ensure medical review and input for all promotional and non-promotional initiatives.
 </li>
 <li>
 Provide support for field queries, product claims, and new portfolio launches.
 </li>
 </ul>
 
 
 
 
 
 Desired Skills &amp; Competencies
 
 
 <ul>
 <li>
 Strong scientific knowledge in pediatrics, vaccines, nutrition, and preventive health.
 </li>
 <li>
 Excellent scientific writing, training, and presentation skills.
 </li>
 <li>
 Ability to translate complex science into impactful messaging for doctors and sales teams.
 </li>
 <li>
 Proficiency in compliance frameworks and regulatory documentation.
 </li>
 <li>
 Influencing and relationship-building skills with KOLs and internal stakeholders.
 </li>
 </ul>
 
 
 
 
 
 Key Performance Indicators (KPIs)
 
 
 <ul>
 <li>
 Effectiveness of sales force training (measured by knowledge assessments &amp; field performance).
 </li>
 <li>
 Number and quality of KOL engagements and CME activities.
 </li>
 <li>
 Accuracy, timeliness, and compliance of scientific content reviews.
 </li>
 <li>
 Contribution to new product launches and evidence generation.
 </li>
 <li>
 Internal feedback on scientific and strategic support.
 </li>
 </ul>
 
 
</div>

Medical Affairs Manager

Amazon

<div>
 
 Description
 
 
 
 We seek a strong and experienced leader to manage medical affairs of the businesses under Amazon Medical. We are on a mission to invent the most patient centric healthcare service. This role will directly report to the head of Amazon Medical and is expected play a critical role in helping the operating team understand, appreciate and navigate the medical space with the right expertise and insights.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Execute the Amazon Medical&rsquo;s vision and strategy for superior integrated care delivery.
 </li>
 <li>
 Build the right level of medical awareness and knowledge to the rest of the non-medical business folks who are building critical pieces of this business.
 </li>
 <li>
 Build mechanisms to ensure the highest standards of clinical quality and medical compliance.
 </li>
 <li>
 Make effective use of technology and analytical tools to assess, support, and report the status of Quality, Safety and Risk Management; ensuring the accuracy and reliability of all data used for internal and any required external reporting purposes.
 </li>
 <li>
 Investigate new developments in medical care practices and techniques that can be applied to current and future programs.
 </li>
 <li>
 Evaluate technology solutions for clinical appropriateness, providing guidance on potential uses for Amazon's programs and limitations of new technologies.
 </li>
 <li>
 Ensure accountability for results, integrity, compliance and quality.
 </li>
 <li>
 Evaluate developments in medical care and make recommendations for innovative practices and procedures.
 </li>
 <li>
 Develop personal and professional credibility to gain respect and build trust between the Amazon, community partners and the broader medical community.
 
 
 </li>
 </ul>
 The role holder is expected to to be MBBS doctor with an active practising license.
 
 
 The role is not a pure-play SME (subject matter expert) responsiblity. The candidate will be expected to proficient with data crunching, project management and working deeply with a large passionate team.
 
 
 
 Basic Qualifications
 
 
 
 <ul>
 <li>
 3+ years of program or project management experience
 </li>
 <li>
 3+ years of working cross functionally with tech and non-tech teams experience
 </li>
 <li>
 3+ years of defining and implementing process improvement initiatives using data and metrics experience
 </li>
 <li>
 Bachelor's degree
 </li>
 <li>
 Knowledge of Excel (Pivot Tables, VLookUps) at an advanced level and SQL
 </li>
 <li>
 Experience defining program requirements and using data and metrics to determine improvements
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 3+ years of driving end to end delivery, and communicating results to senior leadership experience
 </li>
 <li>
 3+ years of driving process improvements experience
 </li>
 <li>
 Experience in stakeholder management, dealing with multiple stakeholders at varied levels of the organization
 </li>
 <li>
 Experience building processes, project management, and schedules
 
 
 </li>
 </ul>
 Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you&rsquo;re applying in isn&rsquo;t listed, please contact your Recruiting Partner.
 
 
 
 
 Company
 
 - ASSPL - Karnataka
 
 
 Job ID: A3070454
</div>

Medical Affairs Manager, Amazon Medical

Amazon.com

<div><h2 class="jobSectionHeader">DESCRIPTION</h2>
We seek a strong and experienced leader to manage medical affairs of the businesses under Amazon Medical. We are on a mission to invent the most patient centric healthcare service. This role will directly report to the head of Amazon Medical and is expected play a critical role in helping the operating team understand, appreciate and navigate the medical space with the right expertise and insights. 
 
Key responsibilities: 
Execute the Amazon Medical&rsquo;s vision and strategy for superior integrated care delivery. 
Build the right level of medical awareness and knowledge to the rest of the non-medical business folks who are building critical pieces of this business. 
Build mechanisms to ensure the highest standards of clinical quality and medical compliance. 
Make effective use of technology and analytical tools to assess, support, and report the status of Quality, Safety and Risk Management; ensuring the accuracy and reliability of all data used for internal and any required external reporting purposes. 
Investigate new developments in medical care practices and techniques that can be applied to current and future programs. 
Evaluate technology solutions for clinical appropriateness, providing guidance on potential uses for Amazon's programs and limitations of new technologies. 
Ensure accountability for results, integrity, compliance and quality. 
Evaluate developments in medical care and make recommendations for innovative practices and procedures. 
Develop personal and professional credibility to gain respect and build trust between the Amazon, community partners and the broader medical community. 
 
The role holder is expected to to be MBBS doctor with an active practising license.
 
 
The role is not a pure-play SME (subject matter expert) responsiblity. The candidate will be expected to proficient with data crunching, project management and working deeply with a large passionate team.<h2 class="jobSectionHeader">
BASIC QUALIFICATIONS</h2><ul><li>3+ years of program or project management experience</li><li>3+ years of working cross functionally with tech and non-tech teams experience</li><li>3+ years of defining and implementing process improvement initiatives using data and metrics experience</li><li>Bachelor's degree</li><li>Knowledge of Excel (Pivot Tables, VLookUps) at an advanced level and SQL</li><li>Experience defining program requirements and using data and metrics to determine improvements</li></ul><h2 class="jobSectionHeader">
PREFERRED QUALIFICATIONS</h2><ul><li>3+ years of driving end to end delivery, and communicating results to senior leadership experience</li><li>3+ years of driving process improvements experience</li><li>Experience in stakeholder management, dealing with multiple stakeholders at varied levels of the organization</li><li>Experience building processes, project management, and schedules</li></ul> 
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you&rsquo;re applying in isn&rsquo;t listed, please contact your Recruiting Partner.</div>

Ajanta Pharma Ltd

<div>
 
 
 Job Title: General Manager - Medical Affairs
 
 
 
 Location: Mumbai
 
 
 Company: Ajanta Pharma LTD
 
 
 Reports to: India Business Head
 
 
 
 
 
 
 Job Summary:
 
 
 
 The General Manager of Medical Affairs will lead the medical affairs strategy at Ajanta, focusing on providing robust medico-marketing support and facilitating collaboration between the medical and marketing teams. This role will encompass the development of medical materials, training programs, and evaluation of new products, ensuring alignment with the company's business goals and compliance with regulatory standards.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 1. Medico-Marketing Support: o Provide medical references and data to support product positioning and new product research and development (NPD).
 
 
 2. Marketing Collaboration: o Support the marketing team with regular inputs and strategic advice on promotional activities to ensure accurate messaging and compliance.
 
 
 3. Material Preparation: o Prepare comprehensive product manuals, product monographs, and training slides to enhance understanding and communication of product benefits.
 
 
 4. CME Development: o Develop and prepare Continuing Medical Education (CME) slides and materials to support ongoing education initiatives.
 
 
 5. Product Evaluation: o Evaluate new product ideas and presentations, providing insights and recommendations to the marketing and business development teams.
 
 
 6. Training Sessions: o Conduct medical training sessions for field staff to ensure they are well-informed about products and therapeutic areas.
 
 
 7. Clinical Study Participation: o Actively participate in clinical studies to gather relevant data and insights that inform medical affairs strategies.
 
 
 8. Competitive Analysis: o Conduct evaluations of competitors&rsquo; new products and strategies, providing analysis to inform company positioning and development efforts.
 
 
 9. Market Intelligence: Monitor industry trends, competitor activities, and emerging science to provide insights that drive strategic decisions.
 
 
 10. Budget Management: Develop and manage the budget for the medical affairs department, ensuring efficient use of resources.
 
 
 11. Stakeholder Engagement: Build and maintain relationships with key opinion leaders, healthcare professionals, and relevant organizations to enhance scientific communication and brand credibility.
 
 
 
 
 
 
 Qualifications:
 
 
 
 &bull; Education: Advanced degree in life sciences (MBBS, MD) or equivalent.
 
 
 &bull; Experience: Minimum of 15 years in medical affairs or related fields, with a focus on marketing support and product evaluation.
 
 
 &bull; Knowledge: Strong understanding of regulatory requirements, clinical development processes, and the therapeutic landscape relevant to the company&rsquo;s products.
 
 
 &bull; Skills: Excellent communication, presentation, and interpersonal skills; ability to work collaboratively across teams and influence stakeholders. &bull; Analytical Skills: Strong analytical and critical thinking abilities to assess data and inform strategic decisions. Preferred
 
 
 &bull; Familiarity with developing training programs and CME materials.
 
 
 
 
 
 
 What We Offer:
 
 
 
 &bull; Competitive salary and benefits package.
 
 
 &bull; Opportunities for professional development and career advancement.
 
 
 &bull; A dynamic and collaborative work environment.
 
</div>

General Manager - Medical Affairs

Sanofi

<div>Job Title: Field Medical Manager - Rare Diseases
Location: Istanbul
About the Job
The Field Medical Manager is a field-based medical professional responsible for engaging with Key Opinion Leaders (KOLs), Health Care Professionals (HCPs), and regional/local institutions through high-level scientific exchange. This includes medical education, research collaboration, publications, consultancy, and other Medical Affairs initiatives aligned with company strategy.
Main Responsibilities<ul><li>
Establish and maintain scientific relationships with KOLs, HCPs, and relevant institutions in the assigned territory.</li><li>
Actively contribute to training programs, research projects, publications, and consultancy activities.</li><li>
Facilitate effective cross-functional communication to support the implementation of Medical Affairs strategies.</li><li>
Provide comprehensive medical and scientific support across internal teams.</li><li>
Represent Sanofi as a &ldquo;Scientific Ambassador&rdquo; in all external engagements.</li></ul>
About You<ul><li>
Medical degree (MD) is required.</li><li>
Fluent in Turkish and English (both verbal and written).</li><li>
Must be able to travel extensively.</li><li>
Excellent communication skills, including verbal, written, and public speaking abilities.</li><li>
Strong ability to analyze and interpret clinical and preclinical data.</li><li>
Collaborative mindset with a strong ability to work in cross-functional teams.</li><li>
Proactive and solution-oriented approach in a dynamic medical environment.</li><li>
Demonstrated ability to build and maintain strong relationships with both external and internal stakeholders.</li></ul>
What Sanofi Can Offer You 
<ul><li>
Benefits to enhance your life journey</li><li>
Development opportunities to own your future</li><li>
An open and inclusive environment where you can be yourself</li><li>
Social activities and wellbeing programs to support your life</li></ul> 
We chase the miracles of science to improve people&rsquo;s lives. 
 
We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people&rsquo;s lives. 
 
Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to make the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our commitments. 
 
We are one of the largest pharmaceutical companies in Turkey, serving public health for with more than 1,600 employees. Adding value to local economy and development in Turkey, we offer a broad range of products including innovative therapeutic solutions, biotechnological pharmaceuticals, vaccines, and consumer healthcare products. 
 
Our factory in L&uuml;leburgaz is one of the leading pharmaceutical manufacturing plants in Turkey. It is also among the top three Sanofi production sites worldwide in terms of its manufacturing capacity. Our manufacturing site, produces high-quality pharmaceuticals in many different forms in accordance with global health standards, and develops generic medicine at its on-site R&amp;D Center. 
 
Pursue progress. 
 
Discover extraordinary. 
 
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles. 
 
So let&rsquo;s be those people. 
 
Let&rsquo;s explore more, and share a purpose, as well as our skills. Let&rsquo;s reinvent healthcare, chase change, and embrace new ideas. Let&rsquo;s take bigger risks and find better solutions for the people we help. 
 
Let&rsquo;s pursue progress. 
 
And let&rsquo;s discover extraordinary, together.
null</div>

Field Medical Manager (RD)

Takeda Pharmaceuticals

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2>
About the Role
The Medical Therapy Area Lead is the most senior role on the Medical Affairs team and reports directly into the country Medical Head. The TA Lead is responsible for developing and executing Medical Affairs strategies for the East Gulf and Levant cluster in the Gastroenterology and Hereditary Angioedema (HAE) therapeutic areas. This role plays a pivotal part in shaping and implementing strategic medical plans that support Takeda&rsquo;s mission of delivering better health and a brighter future. Success will depend on strong cross-functional collaboration with Commercial teams, alignment with Area and Regional Medical functions, and building trusted partnerships with external stakeholders.
How you will contribute:
Scientific Leadership<ul><li>
Craft and execute the medical communication plan. This includes delivering medical education and developing scientific platforms,</li><li>
Earn and maintain credibility through continuous learning, thought leadership, and presence in professional forums</li><li>
Provide strong medical insights to inform clinical research activities and contribute to evidence generation strategies.</li></ul>
Stakeholder engagement<ul><li>
Identification &amp; Segmentation: Define specific objectives and determine which stakeholder groups can help achieve them.</li><li>
Segment stakeholders, including KOLs, HCPs, payers, regulators, patient groups, and digital opinion leaders, by their roles and influence level.</li><li>
Conduct mapping exercises to understand each stakeholder&rsquo;s interests and potential impact.</li></ul><ul><li>
Develop and implement TL engagement programs, particularly in pre-launch and launch phases.</li><li>
Build strong partnerships with healthcare professionals, scientific societies, and patient groups (where applicable).</li><li>
Drive advisory boards, scientific partnerships, and publication strategies to shape treatment pathways and patient care.</li><li>
Support product registration, and formulary inclusion.</li><li>
Ensure robust pre-approval and launch readiness activities in collaboration with Commercial and cross-functional teams.</li></ul>
Organizational Excellence:<ul><li>
Approve promotional and non-promotional materials, activity, and engagement requests</li></ul><ul><li>
Establish and maintain a culture of compliance, ensuring adherence to Takeda&rsquo;s Code of Conduct, local regulations, and industry best practices.</li><li>
Oversee implementation and compliance with Medical Affairs SOPs</li><li>
Ensure timely follow-up, tracking, and reporting of adverse events in accordance with PV standards.</li><li>
Serve as a strategic bridge for aligning priorities across functions</li></ul><ul><li>
Lead Medical Affairs input into Named Patient Programs and early access initiatives.</li><li>
Design and execute regular audits of Medical Affairs processes to ensure compliance and operational excellence.</li></ul><ul><li>
Implement corrective actions and continuous improvement initiatives as required</li><li>
Use virtual tools: online forums, digital opinion leaders (DOLs), webinars, AI-powered chatbots, and e-learning modules.</li><li>
Adhere to allocated budget and ensure funds are directed toward high-value activities that advance scientific and patient objectives.</li></ul>
Major Challenges<ul><li>
Supporting multiple new product launches and indications in a fast-paced environment.</li><li>
Building medical capabilities in new therapeutic areas</li><li>
Ensuring effective cross-functional collaboration and alignment across local, regional, and global teams.</li><li>
Establishing Medical Affairs as strategic business partners across the organization.</li></ul>
Qualifications &amp; Experience<ul><li>
Medical advisor level and above</li><li>
Medical degree (PharmD, PhD, or MD or equivalent) required; relevant postgraduate degree (e.g., Master&rsquo;s degree in a specialty) strongly preferred.</li><li>
Experience in gastroenterology or rare diseases strongly preferred</li><li>
Experience managing multiple countries with diverse healthcare systems, strongly preferred</li><li>
Minimum 10 years&rsquo; professional experience, including at least 5&ndash;6 years in Medical/Scientific Affairs within a reputable mid- to large-sized organization.</li><li>
Demonstrated experience leading teams, driving medical strategy, and managing stakeholders across complex healthcare environments.</li></ul>
Required Capabilities<ul><li>
Strategic thinker with strong innovation and execution capabilities.</li><li>
Proven ability to manage multiple complex initiatives under pressure.</li><li>
Exceptional leadership, coaching, and team development skills.</li><li>
Strong interpersonal, communication, and relationship-building abilities.</li><li>
Goal-oriented, energetic, and resilient.</li><li>
Highly process- and compliance-oriented.</li></ul>
As an expert professional within the organization, you develop innovative solutions to complex problems aligned with organizational objectives. Your work involves addressing intricate issues, requiring in-depth analysis and judgment. You also engage with key contacts outside your expertise area and contribute to the development of new concepts and standards. Operating with considerable autonomy, you serve as a consultant to management and an external spokesperson on major matters, often working independently and leading function teams or projects. Additionally, you play a role in training and mentoring junior staff.<h2 class="jobSectionHeader">
Locations</h2>
Dubai, UAE<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

Medical Therapy Area Lead – GI/HAE, East Gulf & Levant

Takeda

<div>
 By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
 
 
 
 Job Description:
 
 
 
 Are you passionate about leading with purpose, inspiring scientific excellence, and driving impactful medical strategies? Takeda T&uuml;rkiye is searching for a visionary
 
 Country MSL Manager:
 
 to lead our Medical Science Liaison (MSL) team. This is your opportunity to join an organization deeply committed to improving patients&rsquo; lives while fostering collaboration, innovation, and trust.
 
 
 
 Key Responsibilities:
 
 
 
 
 Core Responsibilities:
 
 
 
 <ul>
 <li>
 
 Strategic Leadership:
 
 </li>
 <ul>
 <li>
 Translate country medical strategy and therapeutic area (TA) objectives into operational field medical plans.
 </li>
 <li>
 Oversee execution of annual MSL territory plans, ensuring strategic engagement with key external stakeholders.
 </li>
 <li>
 Partner cross-functionally with Medical Strategy, Brand Managers, Market Access, and Integrated Patient Solutions teams to align priorities.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Team Management:
 
 </li>
 <ul>
 <li>
 Recruit, onboard, and train MSLs, fostering a high-performing, collaborative, and customer-oriented culture.
 </li>
 <li>
 Conduct regular performance reviews, provide coaching, and set visible qualitative and quantitative Key Performance Indicators (KPIs).
 </li>
 <li>
 Identify developmental needs within the team and implement targeted training programs.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Operational Excellence:
 
 </li>
 <ul>
 <li>
 Ensure consistent, compliant documentation of MSL activities in the CRM system.
 </li>
 <li>
 Implement metrics/reporting to track performance and communicate the team&rsquo;s value to stakeholders.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Scientific Engagement:
 
 </li>
 <ul>
 <li>
 Maximize MSL interaction capabilities by prioritizing high-quality time spent with healthcare providers (HCPs).
 </li>
 <li>
 Enhance trust in Takeda through credible scientific discussions that build company reputation.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Representation:
 
 </li>
 <ul>
 <li>
 Represent the MSL team at local (e.g., therapeutic area team, medical leadership) and global medical affairs meetings.
 
 </li>
 </ul>
 </ul>
 
 Mandatory Responsibilities:
 
 
 
 <ul>
 <li>
 
 Compliance &amp; Integrity:
 
 </li>
 <ul>
 <li>
 Ensure all MSL activities comply with industry codes, company policies, and local regulations.
 </li>
 <li>
 Lead compliance awareness in the MSL team while exemplifying ethical conduct in line with Takeda values (Takeda-ism).
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Quality &amp; System Use:
 
 </li>
 <ul>
 <li>
 Act as a Quality Ambassador by reporting product-related concerns to the Quality team in a timely manner.
 </li>
 <li>
 Encourage process discipline across the team by promoting timely and accurate use of systems like Concur, Dakika, and Bloom.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 
 Training &amp; Reporting:
 
 </li>
 <ul>
 <li>
 Complete all mandatory training requirements and ensure team-wide adherence to policies and procedures.
 </li>
 <li>
 Proactively raise compliance or ethical concerns through the appropriate Takeda reporting channels.
 
 </li>
 </ul>
 </ul>
 
 Qualifications:
 
 
 
 <ul>
 <li>
 A degree in Medicine or Pharmacy (PhD strongly preferred).
 </li>
 <li>
 7+ years of medical affairs or clinical development expertise within the pharmaceutical industry.
 </li>
 <li>
 Demonstrated leadership experience, including team management or project mentorship.
 </li>
 <li>
 Strong verbal and written communication in English and Turkish.
 </li>
 <li>
 Robust knowledge of the pharmaceutical business, market access nuances, and developing compliant strategies.
 </li>
 <li>
 Proficiency with CRM tools, field dashboards, and remote engagement platforms.
 </li>
 <li>
 A valid B-class driver&rsquo;s license and willingness to travel.
 
 
 </li>
 </ul>
 
 Locations:
 
 
 
 Istanbul, Turkey
 
 
 
 Worker Type:
 
 
 
 Employee
 
 
 
 Worker Sub-Type:
 
 
 
 Regular
 
 
 
 Time Type:
 
 
 
 Full time
</div>

Country MSL Manager

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Medical Therapy Area Lead – GI/HAE, East Gulf & Levant

Country MSL Manager