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Boehringer Ingelheim

<div>We are looking for a Medical Advisor to join our medical affairs team, for Specialty and Rare Diseases therapeutic area, based in &#304;stanbul, T&uuml;rkiye . This position will be responsible for developing, implementing and executing short- and long-term medical goals and tactics, with an emphasis on pharmacotherapeutic aspects and with understanding of business priorities. Key aspects of this role also include providing medical knowledge and scientific updates to support in collaboration with selected healthcare professionals and cross-functional teams. 
 
This position reports to the Medical Affairs Manager. 
 
 
 
Responsibilities
<ul><li>Implement and execute short- and long-term medical goals and tactics, with an emphasis on pharmacotherapeutic aspects and with an understanding of business priorities.
</li><li>Act as health care manager responsible for health care compliance revision and approval of commercial communication.
</li><li>Provide scientific leadership in cross-functional TA Brand team and contribute to the country strategy for brand medical plans.
</li><li>Provide medical knowledge and scientific update within the therapy areas for external stakeholders &amp; scientific information management and dissemination.
</li><li>Scientific collaboration with selected healthcare professionals (EE: External Experts) within the therapy area with the objectives of educational programs
</li><li>Competitor intelligence sharing with internal groups.
</li><li>Internal training for commercial colleagues and coaching MSLs
</li><li>Maintaining scientific expertise within the cross-functional team
</li><li>Responding to medical information requests and archiving of relevant documentation and correspondence
</li><li>R&amp;D consulting for clinical research.
</li><li>Make presentations regarding HCP Activities.
</li><li>Lead the scientific discussion in the cross-functional team with internal and external stakeholders in the format require e.g. Letters, meetings, etc.
</li><li>Advocating company image to scientific community and Health authorities
</li><li>Participating in scientific congresses, symposia, trainings and representing the company
</li>Maintains a code of professional conduct as a medical practitioner and reports instances of unethical practices exhibited by competitors. 
<li>
</li></ul>Requirements
<ul><li>Degree in Medicine
</li><li>Minimum 2 years of experience in Medical Affairs; Advisor or Sr. Regional Medical Manager/ Sr. MSL experience is a plus
</li><li>Experience in Specialty Care is a plus
</li><li>Professional p roficiency in English with excellent communication and influencing skills
</li>High level of analytical and reasoning skills 
<li>
</li></ul>What happens Next?
We are looking forward to receiving your application! We will then have a look at your CV. If we see a match, we will invite you for a screening interview.
 
 
SPL Screening:
In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (&ldquo;SPL&rdquo;). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.</div>

Medical Advisor

AbbVie

<div>Company Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. 
Job Description 
 We are looking for team members who are located Istanbul or Ankara.<ul><li>
Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts of strategic importance to AbbVie.</li><li>
Ensure a strong medical and scientific presence for AbbVie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie.</li><li>
Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific up-to-date presentations. Work collaboratively and cross-functionally with other in-field members while retaining functional independence.</li><li>
Attend relevant scientific meetings and Conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives.</li><li>
Develop and maintain collaborative relationships with thought leaders in the product / therapeutic area for which the MSL has been assigned responsibility, to facilitate AbbVie research and educational priorities and strategic initiatives.</li></ul> 

Qualifications 
<ul><li>
University degree in Medicine or Pharmacy,</li><li>
Previous experience in academy and/or pharma industry would be an asset</li><li>
Fluency in English,</li><li>
Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general,</li><li>
Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company,</li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li></ul> 

Additional Information<div></div> 
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html</div>

Medical Science Liaison

Eli Lilly

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.<div>
JOB RESPONSIBILITIES</div><div></div><div><div><div><div><div><div><div><div><div>
Brand Team Support<ul><li>
Serve as a key medical point of contact for the brand team.</li><li>
Contribute clinical, scientific, and strategic input to support the cross functional team.</li><li>
Medical launch support</li><li>
By offering scientific and creative input, contribute to the development (local materials) and/or review (global/regional materials) of promotional materials for the brand teams.</li><li>
Effectively communicate and transfer knowledge of the therapeutic available solutions environment, the clinical landscape and relevant medical and scientific information</li><li>
Support the medical training needs of internal business partners such as sales and marketing.</li><li>
Support the planning &amp; implementation of symposia, advisory boards, scientific exchange, and educational meetings/events with HCP&rsquo;s.</li></ul>
Customer Support &amp; Experience<ul><li>
Respond to external customer questions and needs, including escalations by Med Info &amp; sales in accordance with company-wide requirements for responding to unsolicited requests for information.</li><li>
The local coordination of activities and engagement of Thought Leaders</li><li>
Speaker training</li><li>
Develop and maintain collaborations and relationships with relevant professional societies.</li><li>
Deliver scientific, educational, and promotional presentations internally and to customers.</li><li>
Collaborate cross-functionally to drive improvement in customer engagement through Digital innovation.</li><li>
Oversee the collation and analysis of customer information to drive understanding and insights.</li></ul>
Scientific Expertise and Medical Affairs Delivery<ul><li>
Develop and/or contribute to the affiliate / therapeutic area medical plan and strategies.</li><li>
Support data analysis and the development of slide sets and publications (abstracts, posters, manuscripts)</li><li>
Keep up to date with medical and other scientific developments relevant to the product or portfolio.</li><li>
Be aware of current trends, issues and projections for clinical practice and access.</li><li>
Partner with other existing medical affairs roles to achieve a seamless medical team aimed at delivering exceptional customer experiences.</li><li>
May serve as the affiliate medical/scientific leader including research and regulatory deliverables.</li></ul>
QUALIFICATIONS<ul><li>
Advanced degree (MD) in health sciences min. 3 years of relevant clinical, therapeutic experience or relevant scientific industry experience</li><li>
Cardiometabolic Health experience preferred</li><li>
Good planning and organization skills</li><li>
Strong communication skills</li><li>
Ability to effectively partner across multiple functions.</li><li>
Advanced interpersonal, project management and presentation skills</li><li>
Fluent in English (both verbal and written)</li><li>
Ability to &lsquo;translate&rsquo; scientific data into meaningful, clear, and compliant content for customer communications and engagement.</li><li>
Commercial/business acumen</li><li>
Location: Based in Istanbul</li></ul></div></div></div></div></div></div></div></div></div>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly</div>

Director - Medical, CMH, Türkiye

Abbott

<div>Medical Scientific Liason
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people&rsquo;s health. We&rsquo;re always looking towards the future, anticipating changes in medical science and technology.
The Opportunity
This position works at Umraniye location in the Established Pharmaceuticals Division that we are committed to bringing the benefits of our trusted medicines to more people in the world&rsquo;s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.
What You&rsquo;ll Do
This position will be based in &#304;stanbul and will cover a broad geographic area around the country. Some of responsibilities are;<ul><li>
Planning, preparing and delivering medical presentations to Key Opinion Leaders and Physicians on their related therapeutic areas.</li><li>
Proactively identifying HCPs with high levels of scientific expertise in local treatment practice to collaborate on specific medico marketing activities,</li><li>
Developing and maintaining high level scientific relationships with Key Opinion Leaders and physicians in his/her region through meetings, congresses, double visits, etc..</li><li>
Supporting sales team to update and develop their scientific and technical expertise and provide adequate medical training whenever necessary.</li><li>
Following up to date literatures and getting information about the latest developments in related therapeutical fields.</li></ul>
Required Qualifications<ul><li>
University degree in Medical or Pharmacy Faculty</li><li>
High motivation to work in pharmaceutical industry</li><li>
Excellent verbal and written communication skills including strong presentation skills</li><li>
Result oriented personality with strong planning, reporting and analytical skills</li><li>
Excellent interpersonal skills, high self-motivation, energy and enthusiasm</li><li>
Good at teamwork</li><li>
Excellent command of written and spoken English</li><li>
Have a valid driving license.</li><li>
No restriction to travel frequently.</li></ul></div>

Medical Scientific Liason

<div>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
JOB SUMMARY 
Medical Science Liaisons (MSL) are field based medical professionals with deep content knowledge about specific disease states, Lilly and competitor compounds along with having knowledge on current issues in the therapeutic areas they represent. MSLs recognize and communicate feedback and insights of strategic importance from their interactions with Scientific Experts, to better inform Lilly&rsquo;s strategic direction for research and commercialization. By facilitating scientific exchange between industry and the scientific community, MSLs have the opportunity to shape the future of healthcare by providing needed information that addresses important clinical and scientific questions.<div> 
JOB RESPONSIBILITIES 
Maintain and effectively communicate deep scientific knowledge: 
<ul><li>Engage and ensure continuous learning to maintain the highest level of technical expertise within their respective therapeutic area. This will enable the MSL.</li><li>Be equipped to answer deep scientific questions and be sought after by their customers based on peer-credible knowledge and expertise.</li><li>To establish oneself as a reliable, trusted, resource of unbiased, accurate, up-to-date, medical and scientific knowledge requested and desired by customers.</li></ul>
Excellence at customer engagement and support medical/scientific information needs of scientific experts:</div><ul><li>Ensure customer facing engagement through mutually beneficial 2-way dialogues with scientific experts.</li><li>Act as the primary interface between Lilly medical and scientific experts to deliver the best-in-class customer experience through application of effective emotional intelligence and deep understanding of customer needs.</li><li>Connect scientific experts with Lilly resources or internal business partners as appropriate and identify possible collaborative research or external collaborations.</li></ul><div>
Strategic vision and leadership: 
<ul><li>Synthesize complex data and effectively communicate meaningful clinical insights and unanswered customer questions received from Scientific Experts to Lilly medical and cross -functional teams (CFT).</li><li>Use reactive problem-solving skills and utilize internal resources effectively to execute upon solutions.</li><li>Use a principle-based decision-making approach to make decisions independently or escalate them appropriately.</li><li>Cultivate internal networks and collaborate effectively across functions with an active contribution to medical planning and strategy in the affiliate.</li></ul></div><div>
Territory ownership: 
<ul><li>Demonstrate strategic analysis, planning, and prioritization to maximize efficiency.</li><li>Implement and evaluate a strategic territory plan prioritizing core activity and take personal accountability for results.</li><li>Execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws, demonstrating good judgement at all times.</li></ul></div><div>
Professional Development: 
<ul><li>Keep up to date on trainings for professional development.</li><li>Ensure Performance Management objectives are completed in line with company process.</li><li>Understanding of all company policies and procedures.</li></ul></div><div> 
JOB QUALIFICATIONS 
EDUCATION 
<ul><li>Medical Doctor</li></ul>
EXPERIENCE 
<ul><li>Proven experience to work as an individual and team contributor.</li><li>Proven experience to engage medical professionals.</li></ul></div><div>
Desirable 
<ul><li>Minimum of 1 years&rsquo; MSL experience within a multinational company.</li><li>Experience in Oncology &amp; Hematology therapeutic areas preferred.</li><li>Experience with academic communities, medical research, and medical education process.</li></ul>
SOFT SKILLS 
<ul><li>High learning agility to comprehend and effectively communicate large amounts of complex scientific content in a clear and concise fashion.</li><li>Independent contributor to be able to work alone in the field effectively managing multiple priorities and projects.</li><li>Strategic and critical thinking to analyze, assess and evaluate information and interpret impact or relevance to future states.</li><li>Strong verbal and written communication skills.</li><li>Resiliency in managing complex challenges.</li><li>Strong teamwork and interpersonal skills.</li><li>High emotional intelligence.</li><li>Strong relationship building and networking.</li><li>Strong planning and organization.</li></ul>
TECHNICAL SKILLS</div><ul><li>Advanced presentation and computer skills with expertise in literature identification.</li><li>Ability to use field-based electronic or other communication tools needed for role.</li></ul>
OTHER QUALIFICATIONS 
<ul><li>Ability to travel 80% of the time (role is pre-dominantly field based)</li><li>Will require domestic travelling and may require international travel.</li><li>May require evening/weekend work.</li></ul>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly</div>

Medical Science Liaison, Oncology, Türkiye

KPMG Türkiye

<div>
 
 KPMG is a global network of professional firms providing Audit, Tax and Advisory services. We operate in 146 countries and have more than 200.000 professionals working in member firms around the world. KPMG is one of the global leaders in Audit, Tax and Advisory services and the chosen business partner for many of the world&rsquo;s leading organizations.
 
 
 
 
 
 Quality and Risk Management (QRM) is a central team and is responsible for setting overall professional risk management and quality control policies and monitoring compliance, ethics and independence. This responsibility includes the need to understand and adhere to policies and associated procedures as well as local law requirements in carrying out their day-to-day activities. This team has an important role in identification, evaluation, management and monitoring of the most significant risks that the Firm faces and could threaten the achievement of its strategic objectives.
 
 
 Legal Affairs Junior Specialist will be an integral part of the QRM team reporting to the Legal Affairs Senior Manager.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 Bachelor's degree in law and admission to the Turkish Bar Association,
 </li>
 <li>
 At least 1 year corporate experience is preferred,
 </li>
 <li>
 Knowledge and experience on standards and regulations issued by authorities (such as Public Oversight Accounting and Auditing Standards Authority, Capital Markets Board and Banking Regulation and Supervision Agency ) and in Data Protection Law,
 </li>
 <li>
 Strong understanding of Turkish Law and practice,
 </li>
 <li>
 Excellent command of English both in verbal and written,
 </li>
 <li>
 Good command of Microsoft Office programs,
 </li>
 <li>
 Proactive and self-motivated profile,
 </li>
 <li>
 Strong follow-up, timeliness,
 </li>
 <li>
 Good communication and teamwork skills.
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 
 
 
 <ul>
 <li>
 Supports Legal Affairs Senior Manager and QRM Legal Team in QRM department in preparing, reviewing, negotiating and finalizing contracts with clients, suppliers or other third parties by taking both legislation and company procedures into consideration,
 </li>
 <li>
 Responds to the legal advice requests on daily business matters under the supervision of the Legal Affairs Senior Manager and QRM Legal Team,
 </li>
 <li>
 Continuously and closely follows up any changes in legislation and assist QRM team to ensure full compliance in business practices of KPMG,
 </li>
 <li>
 With respect to the escalated business and legal disputes, conflicts, litigations and queries; conducts the relevant practical and academic legal searches from relevant sources (such as precedent court decisions, legal books, legal opinions on specific competence areas) Supports in solving quality and risk related conflicts between KPMG and its clients or suppliers, drafts termination notifications,
 </li>
 <li>
 Contributing to the preparation and coordination of compliance reports at both global and local levels, ensuring alignment with internal policies and relevant legal regulations,
 </li>
 <li>
 Providing legal advice on various privacy and data protection issues, including compliance with KVKK, GDPR and data protection laws of other jurisdictions and following national and international legislation regarding the protection of personal data.
 </li>
 </ul>
</div>

Legal Affairs & Compliance Junior Specialist

<div><h1 class="jobSectionHeader">Job Description Summary</h1>
An exciting opportunity for a Regulatory Affairs Specialist, the role will be based in Istanbul, Turkey.<h1 class="jobSectionHeader">
Job Description</h1>
We are the makers of possible
BD is one of the largest global medical technology companies in the world. Advancing the world of health&trade; is our Purpose, and it&rsquo;s no small feat. It takes the imagination and passion of all of us&mdash;from design and engineering to the manufacturing and marketing of our billions of MedTech products per year&mdash;to look at the impossible and find transformative solutions that turn dreams into possibilities.
Why Join Us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you&rsquo;ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a maker of possible with us!
About the role
The Regulatory Specialist is responsible for supporting and driving regulatory activities across multiple projects and product lines. You will be responsible for launching of Medical Device &amp; In-Vitro Diagnostic products in the Turkish market in addition to ensuring the absence of any regulatory issue in alignment with company standards and country regulations. This role ensures compliance with industry standards and regulatory requirements by reviewing and approving advertising and promotional materials, leading regulatory and product-related documentation, along with providing local regulatory support.<h2 class="jobSectionHeader">
Main responsibilities will include :-</h2><ul><li>
Responsible for all regulatory activities including but not limited to pre-registration, registration and re-registration steps in accordance with local regulations and business strategies.</li><li>
Develop and maintain communication system with local stakeholders and regional partners</li><li>
Updating regulatory knowledge due to procedures and changes in local directives.</li><li>
Ensuring all products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post market compliance.</li><li>
Scheduling and prioritizing projects and planning submissions with the corresponding partners.</li><li>
Perform and manage Ad Prom local activities</li><li>
Maintain the reimbursement prosses of Social Security Institute (SSI) on determined periods, collaboratively work with local teams, follow up on the approvals and inform business teams.</li><li>
Keep the local business communication alive regarding registrations and reimbursement updates</li><li>
Participating in relevant organizations representing the company.</li></ul>
About You :-<ul><li>
Bachelor&rsquo;s degree in science, engineering or equivalent.</li><li>
Proficiency in Microsoft Office programs (Word, Excel, PowerPoint)</li><li>
Good command of English both written and verbally</li><li>
Self-motivated and self-confident</li><li>
Effective communicator with strong organizational and problem-solving skills</li><li>
Detail oriented and ability to work independently</li><li>
Medical Device registration employee certification is a nice to have.</li></ul><h2 class="jobSectionHeader">
Click on apply if this sounds like you!</h2>
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.<h2 class="jobSectionHeader">
To learn more about BD visit: https://bd.com/careers</h2>
Required Skills
Optional Skills
.<h1 class="jobSectionHeader">
Primary Work Location</h1>
TUR Istanbul - R&uuml;zgarl&#305;bah&ccedil;e Mah<h1 class="jobSectionHeader">
Additional Locations</h1><h1 class="jobSectionHeader">
Work Shift</h1></div>

Regulatory Affairs Specialist

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