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field medical manager rd

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)

Unilever

<div>
 
 Looking for Your Dream Job? Join The Magnum Ice Cream Company!
 
 
 
 
 Ice Cream Microbiologist
 
 
 
 
 Location:
 
 Sar&inodot;gazi R&amp;D IC
 
 
 
 Terms &amp; Conditions:
 
 Full Time
 
 
 The Ice Cream division at Unilever is preparing to stand on its own, aiming to become an independent, EUR 8.3 billion publicly listed company by the end of 2025. We&rsquo;re on a mission to create the ultimate snacking company. A place where growth, innovation, founder and ownership mentality, and performance are cultivated and rewarded. And where we craft extraordinary ice cream experiences - transforming ordinary moments into lasting memories. Because we know, life tastes better with ice cream.
 
 
 
 About The Magnum Ice Cream Company
 
 
 
 The Magnum Ice Cream Company is all about growth. Growing our business. Growing our customers&rsquo; businesses. Growing our people&rsquo;s careers. Growth begins with empowerment. So we free our people to be innovative, responsible entrepreneurs, driven and equipped to give our consumers more amazing products and unforgettable moments &ndash; and having fun doing it.
 
 
 With 19.000 expert ice cream colleagues and iconic brands like Wall&rsquo;s, Cornetto and Ben &amp; Jerry&rsquo;s, loved in 76 countries, we are the world&rsquo;s largest Ice Cream company leading the industry. We have been taking pleasure seriously for more than 100 years, serving happiness with every lick or scoop of ice cream for generations.
 
 
 We are investing to unlock the full growth potential of The Magnum Ice Cream Company as a standalone entity, once we separate from Unilever, which is planned to happen before the end of 2025.
 
 
 We dream big but keep things simple to act fast.
 
 
 If you want to
 
 grow with us, make an impact, and shape the future of Ice Cream
 
 , this is the place for you!
 
 
 The role sits within the Scientific Affairs team, more specifically the Global Research, Development &amp; Innovation (RD&amp;I) Microbiology Team, and will be based in Sarigazi, Turkey.
 
 
 The Ice Cream business in METSA Region is large and highly successful. The Ice Cream Regional Design Center (RDC) located in Sarigazi/Istanbul is the driving force behind the creation and delivery of benefit-led, innovative ice cream products across our world-renowned global (e.g. Magnum, Cornetto, Twister), premium local (e.g. Carte D&rsquo;or, Maras) and regional (e.g. Vienetta) brands. The team embrace agile innovation and are fully connected to country teams to land innovation and renovation projects in the markets. The team is closely connected to local marketing and customer development teams and support their relationships with regulatory authorities, customers (e.g. by developing compelling selling stories that drive sales of our products) and consumers.
 
 
 The business reaches across all ice cream experiences under two broad platforms: In Home and OOH (in-home tubs, log and pints and out of home experiences such as scooping non portioned and mono portions) and Impulse which includes global and local stick, cup, cone formats under Kids, Snacking, Cone and premium ranges.
 
 
 
 Our Team
 
 
 
 Ensuring that The Magnum Ice Cream Company (TMICC) products are safe to consume is of paramount importance for the business. The Global Scientific Affairs function, which is part of RD&amp;I, brings together Food Safety, Regulatory Affairs and Nutrition expertise to ensure that TMICC products are safe-by-design and compliant with relevant regulations &amp; nutrition requirements. As well as protecting the business, the Scientific Affairs function is also key to unlocking innovations to enable business growth. One of such functions is the Global RD&amp;I Microbiology team.
 
 
 Global RD&amp;I Microbiology is an agile team of enthusiastic world-class scientists who deliver business relevant microbiological solutions underpinning brand innovation programmes, based on scientific and technological capabilities across RD&amp;I and Supply Chain (SC). The strength of the team lies in the integration of microbiological and processing knowledge for RD&amp;I to develop safe/stable formulation &amp; process designs to deliver winning products.
 
 
 The Ice Cream Microbiologist will work within the Global RD&amp;I Microbiology team delivering up-front microbiological solutions and security across our RD&amp;I innovation portfolio and business operations, supporting iconic brands such as Magnum, Cornetto and Ben &amp; Jerry&rsquo;s. This is a critical business need as robust data-driven microbiological support: (1) provides the unlock to maximise value from data (faster and sustainable innovation, incident prevention and mitigation, cost efficiencies), (2) provides a solid basis to perform microbiological risk assessments and (3) enables the business to deliver better for you and planet products.
 
 
 This role will be based in Sarigazi (Turkey), co-located with the Ice Cream Regional Design Center, and reporting into the Global RD&amp;I Microbiology team based in Colworth, UK.
 
 
 
 Job Purpose
 
 
 
 Working as an integral member of our enthusiastic team of microbiologists, you will play a key role in supporting new products and processes development projects in RD&amp;I and providing microbiological support to our global business operations.
 
 
 
 Main Responsibilities Include
 
 
 
 <ul>
 <li>
 Ensure microbiological safety of our Ready-To-Eat ingredients by working closely with our Global and Regional Microbiologists, Suppliers, RD&amp;I project leaders, Quality, Procurement, and Ingredient Specialists to align on procedures, review decontamination processes and validation reports, and provide expert guidance for decontamination and validation procedures, as well as delivering decisions on RTE ingredient approval/rejection.
 </li>
 <li>
 Supporting the METSA Business Unit where RD&amp;I Microbiological expertise is needed and drive compliance with Global Microbiology requirements by working closely with the other colleagues from the Global RD&amp;I Microbiology team for alignment and sharing best practices.
 </li>
 <li>
 Conducting microbiological risk assessment for RD&amp;I support (e.g. product development, RTE discussion) and Supply Chain support (e.g. for incident and process control).
 </li>
 <li>
 Assure microbiological safe and stable products and processes by actively implementing a Safe-By-Design approach.
 </li>
 <li>
 Partner with Global team to identify and adapt new methodologies/process/procedures enabling continuous future fit microbiological data science.
 </li>
 <li>
 Deliver technical input for relevant documents and training materials to ensure renew/maintenance of product &amp; process design knowledge.
 </li>
 <li>
 Designing and supervising laboratory project work which will be done either in-house or in cooperation with third party labs.
 
 
 </li>
 </ul>
 
 What You Need To Succeed
 
 
 
 <ul>
 <li>
 Background (minimum BSc) in Microbiology, Applied Biology, Food Safety, or a closely related science area.
 </li>
 <li>
 Preference for previous experience in Microbiology linked to Food Industry, and understanding of food decontamination processes (thermal and non-thermal). Molecular Biology (DNA sequencing interpretation) is an advantage.
 </li>
 <li>
 Basic working knowledge and experience of using Microsoft Office programs (Word, Excel, PowerPoint and Outlook).
 </li>
 <li>
 Excellent communication skills, written and oral to present in multidisciplinary teams and to various stakeholders, both in English and Turkish. Ability to manage complex stakeholder discussions.
 </li>
 <li>
 Ability to learn and work in fast paced environment with varying priorities and demands, demonstrating problem-solving skills where necessary.
 </li>
 <li>
 Team player with flexible &ldquo;we can&rdquo; attitude, yet, ability to work independently and defend own science-based knowledge in front of stakeholders.
 
 
 </li>
 </ul>
 
 What You Can Expect
 
 
 
 <ul>
 <li>
 A unique mix of global scale &amp; start-up spirit&mdash;&euro;8.3bn powerhouse with an agile, entrepreneurial mindset. We&rsquo;re building a new high growth Ice Cream company from the ground up.
 </li>
 <li>
 Career without limits&mdash;42 markets, international opportunities, and fast tracked growth.
 </li>
 <li>
 A performance-driven culture&mdash;Freedom to act, disrupt and grow &ndash; your success is measured by impact.
 </li>
 <li>
 A company that celebrates joy, innovation, and purpose&mdash;We create extraordinary careers, just like our ice cream creates extraordinary moments.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 As publicly announced, Unilever will separate its Ice Cream business which is expected by the end of 2025. This role will transfer to the new Ice Cream company.
 
 
 
 
 Unilever embraces diversity and encourages applicants from all walks of life. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity
 
 .
 
 
 
 For the recruitment of this position, we would like to emphasize that local conditions apply to the position.
 
 
 
 
 ARE YOU EXCITED TO CRAFT THE ICE CREAM FUTURE?
 
 
 
 To apply, you must do so online. Please do not forget to upload your CV and a motivation letter.
 
 
 Your application will be reviewed against our requirements, and we will be in touch shortly after the closing date to provide you with an update on the status of your application.
 
 
 
 Disclaimer
 
 
 
 
 Equal Opportunity Employer: Unilever is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, or any other basis protected by applicable law, and will not be discriminated against on the basis of disability.
 
 
 
 
 We take pleasure seriously. Join the Ice Cream team now!
 
 
 #TMICC
 
 
 
 Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their &lsquo;Whole Self&rsquo; to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.
</div>

Ice Cream Microbiologist

Kerry

<div>
 Requisition ID: 60794
 
 
 Position Type: FT Permanent
 
 
 
 
 About Kerry
 
 
 
 
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 
 
 
 About The Role
 
 
 
 In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.
 
 
 
 
 Key responsibilities
 
 
 
 
 <ul>
 <li>
 Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.
 </li>
 <li>
 Support border clearance of import/export consignments by working closely with customs and relevant authorities.
 </li>
 <li>
 Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).
 </li>
 <li>
 Monitor changes in the food regulations and pro&hyphen;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.
 </li>
 <li>
 Ensure continuous regulatory intelligence and knowledge sharing across the organization.
 </li>
 <li>
 Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes
 </li>
 <li>
 Support New Product Development through participation at product brief and artwork development stages.
 </li>
 <li>
 Provide expertise and direction on product classification and product claims during the NPD Process.
 
 
 </li>
 </ul>
 
 Qualifications And Skills
 
 
 
 <ul>
 <li>
 Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues
 </li>
 <li>
 Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy
 </li>
 <li>
 Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.
 </li>
 <li>
 Experience in working with the government (Turkey &amp; CIS Food Authorities)
 </li>
 <li>
 Expert observation, analysis and judgement (i.e., analytical and objective mind-set)
 </li>
 <li>
 Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS
 </li>
 <li>
 Ability to work with cross-functional teams within the organization at all levels
 </li>
 <li>
 Must be able to speak and write in Russian &amp; English
 
 
 </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 
 
 
 Recruiter
 
 
 
 
 Posting Type:
 
 LI
 
 
</div>

Regulatory Scientist Turkey & CIS

<div>Requisition ID: 60794 
Position Type: FT Permanent 
Workplace Arrangement: #LI-Onsite
<div><div><div><h2 class="jobSectionHeader">
About Kerry</h2>
</div><div>Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.</div></div><div><div><h2 class="jobSectionHeader">
About the role</h2>
</div><div>
In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.</div></div><div><div><h2 class="jobSectionHeader"> 
Key responsibilities</h2>
</div><div><ul><li>Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.</li>
<li>Support border clearance of import/export consignments by working closely with customs and relevant authorities.</li>
<li>Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).</li>
<li>Monitor changes in the food regulations and pro&#8208;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.</li>
<li>Ensure continuous regulatory intelligence and knowledge sharing across the organization.</li>
<li>Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes</li>
<li>Support New Product Development through participation at product brief and artwork development stages.</li>
<li>Provide expertise and direction on product classification and product claims during the NPD Process.</li></ul></div></div><div><div><h2 class="jobSectionHeader"> 
Qualifications and skills</h2>
</div><div><ul><li>Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues</li>
<li>Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy</li>
<li>Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.</li>
<li>Experience in working with the government (Turkey &amp; CIS Food Authorities)</li>
<li>Expert observation, analysis and judgement (i.e., analytical and objective mind-set)</li>
<li>Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS</li>
<li>Ability to work with cross-functional teams within the organization at all levels</li>
<li>Must be able to speak and write in Russian &amp; English</li>
</ul></div></div></div>
Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
Recruiter: #LI-RG1 
Posting Type: LI</div>

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>
Job Purpose 
Act as a trusted scientific partner in the field by engaging healthcare professionals in peer-to-peer scientific exchange, driving insights collection, and supporting local evidence generation, under the strategic guidance of the Medical Manager and in alignment with the Medical Affairs plan.
Role Core Responsibilities &amp; Accountabilities<ul><li>
Establish and maintain peer-to-peer relationships with HCPs, acting as a scientific resource and trusted partner in assigned territory.</li><li>
Plan and execute territory-level KOL engagement aligned with the local medical plan, brand strategy, and scientific priorities.</li><li>
Facilitate timely, accurate, fair-balanced scientific exchange and medical education aligned with compliance standards.</li><li>
Gather, analyze, and share actionable medical insights from HCPs to inform cross-functional planning and R&amp;D alignment.</li><li>
Represent Takeda at scientific meetings and congresses, providing internal summaries and follow-up insights.</li><li>
Deliver training on disease area, clinical data, and product information to commercial, access, regulatory, and patient services colleagues.</li><li>
Provide scientific support for company-sponsored clinical trials and investigator-initiated research, including feasibility, site interaction, and education.</li><li>
Maintain updated knowledge of therapeutic area and treatment landscape, contributing to internal medical intelligence.</li><li>
Accurately document field activities and HCP interactions using CRM tools, ensuring alignment with SOPs and compliance policies.</li><li>
Collaborate with cross-functional teams to support local initiatives such as advisory boards, speaker training, and patient-focused projects.</li></ul>
Role Mandatory Responsibilities<ul><li>
To act in-line with Takeda&rsquo;s &ldquo;Information Security Policy&rdquo; and &ldquo;Acceptable Use of Technology Policy&rdquo;.</li><li>
Being a Quality and Safety Ambassador by identifying and promptly communicating product quality and pharmacovigilance issues to appropriate internal teams.</li><li>
Excels in ethical behavior by consistently acting with integrity and serving as a role model for Takeda-ism values and ethical decision-making.</li><li>
Training &amp; Compliance: Ensure full and timely completion of all mandatory Takeda training requirements and compliance with global, regional, and local procedures and SOPs.</li><li>
Speak-up for Integrity: Encourage a culture of openness by raising any concerns in good faith via the Ethics Line, to line management or directly to Ethics &amp; Compliance.</li></ul>
Job Dimension<ul><li>
OPEX responsibility: YES</li><li>
Financial Responsibility: YES</li><li>
Volume Impact: No</li><li>
Revenue Impact: No</li></ul>
Role required Qualifications &amp; Capabilities<ul><li>
University degree in Medicine or Pharmacy, advanced scientific degree preferred.</li><li>
Demonstrated ability to effectively engage and communicate with KOLs and external medical stakeholders.</li><li>
Highly qualified presentation skills</li><li>
Strong verbal and written communication skills in English and local language.</li><li>
Understanding of relevant therapeutic area, clinical data interpretation, and real-world evidence.</li><li>
Excellent planning, time management, and prioritization skills in a remote/field-based setup.</li><li>
Digital literacy in CRM systems, Microsoft Office, and virtual communication tools.</li><li>
Strong ethical standards and compliance-driven mindset.</li><li>
Minimum 2 years of experience in Medical Affairs or relevant clinical/research environment in the pharmaceutical industry is preferred.</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Istanbul, TurkeyAnkara, Turkey<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 Science Liaison (HAE)

<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>
Job Purpose
Act as a trusted scientific partner in the field by engaging healthcare professionals in peer-to-peer scientific exchange, driving insights collection, and supporting local evidence generation, under the strategic guidance of the Medical Manager and in alignment with the Medical Affairs plan.
Role Core Responsibilities &amp; Accountabilities<ul><li>
Establish and maintain peer-to-peer relationships with HCPs, acting as a scientific resource and trusted partner in assigned territory.</li><li>
Plan and execute territory-level KOL engagement aligned with the local medical plan, brand strategy, and scientific priorities.</li><li>
Facilitate timely, accurate, fair-balanced scientific exchange and medical education aligned with compliance standards.</li><li>
Gather, analyze, and share actionable medical insights from HCPs to inform cross-functional planning and R&amp;D alignment.</li><li>
Represent Takeda at scientific meetings and congresses, providing internal summaries and follow-up insights.</li><li>
Deliver training on disease area, clinical data, and product information to commercial, access, regulatory, and patient services colleagues.</li><li>
Provide scientific support for company-sponsored clinical trials and investigator-initiated research, including feasibility, site interaction, and education.</li><li>
Maintain updated knowledge of therapeutic area and treatment landscape, contributing to internal medical intelligence.</li><li>
Accurately document field activities and HCP interactions using CRM tools, ensuring alignment with SOPs and compliance policies.</li><li>
Collaborate with cross-functional teams to support local initiatives such as advisory boards, speaker training, and patient-focused projects.</li></ul>
Role Mandatory Responsibilities<ul><li>
To act in-line with Takeda&rsquo;s &ldquo;Information Security Policy&rdquo; and &ldquo;Acceptable Use of Technology Policy&rdquo;.</li><li>
Being a Quality and Safety Ambassador by identifying and promptly communicating product quality and pharmacovigilance issues to appropriate internal teams.</li><li>
Excels in ethical behavior by consistently acting with integrity and serving as a role model for Takeda-ism values and ethical decision-making.</li><li>
Training &amp; Compliance: Ensure full and timely completion of all mandatory Takeda training requirements and compliance with global, regional, and local procedures and SOPs.</li><li>
Speak-up for Integrity: Encourage a culture of openness by raising any concerns in good faith via the Ethics Line, to line management or directly to Ethics &amp; Compliance.</li></ul>
Job Dimension<ul><li>
OPEX responsibility: YES</li><li>
Financial Responsibility: YES</li><li>
Volume Impact: No</li><li>
Revenue Impact: No</li></ul>
Role required Qualifications &amp; Capabilities<ul><li>
University degree in Medicine or Pharmacy, advanced scientific degree preferred.</li><li>
Demonstrated ability to effectively engage and communicate with KOLs and external medical stakeholders.</li><li>
Highly qualified presentation skills</li><li>
Strong verbal and written communication skills in English and local language.</li><li>
Understanding of relevant therapeutic area, clinical data interpretation, and real-world evidence.</li><li>
Excellent planning, time management, and prioritization skills in a remote/field-based setup.</li><li>
Digital literacy in CRM systems, Microsoft Office, and virtual communication tools.</li><li>
Strong ethical standards and compliance-driven mindset.</li><li>
Minimum 2 years of experience in Medical Affairs or relevant clinical/research environment in the pharmaceutical industry is preferred.</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Istanbul, TurkeyAnkara, Turkey<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 Science Liaison - Rare Genetic Diseases

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>

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