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medical concultant

Clinixexpert

<p>We&rsquo;re looking for English- French-German-Spanish speaking candidates to join our Call Center Team! If you have good communication skills and enjoy making sales, we&rsquo;d love to meet you.</p><p>What we offer:</p><p>Competitive basic salary</p><p>Commission on performance</p><p>Food card</p><p>Transportation</p><p>Apply now and be part of a dynamic, international team!</p><p>Job Type: Full-time</p><p>Pay: From 30,000.00TRY per month</p>

Medical concultant

Novo Nordisk, Inc.

<div><div><div><div><div><p>Regional Medical Manager
</p></div></div></div></div><div><div><div><div><b>Category: </b>Medical Affairs
</div></div></div></div><div><div><div><div><b>Location:
</b>Ankara, Central Anatolia Region, TR
</div></div></div></div><div><div><div><div><div>Do you have a strong desire to improve care for people with obesity and their quality of life? Would you enjoy facilitating the communication of scientific data and the sharing of knowledge among medical experts in T&uuml;rkiye? Does interacting with leading Medical Doctors and Scientists on an innovative portfolio in obesity interest you? If yes, join us as a Regional Medical Manager on an exciting journey to make a difference in the management of diabetes and obesity. This role is based in Ankara and reports to the Head of Medical and Scientific Affairs.</div><div></div><div><b><br>
Your New Role</b></div>
<div>
The Regional Medical Manager (RMM) is responsible to contribute actively to build, maintain and update scientific knowledge in the therapy area. As a Regional Medical Manager, you will be planning, executing and disseminating up-to-date medical knowledge and clinical trial data, leveraging scientific and clinical expertise with local and regional physicians. You are expected to have the understanding of scientific data for training purposes and are expected to design, help and/or coordinate educational programmes and workshops. You will be working closely with key Opinion Leaders in the area of obesity, helping improve the quality of obesity management in your region of responsibility.<br>
Your key responsibilities will to</div>
<ul>
<li>Develop regional medical advisory services for stakeholders, to increase scientific awareness and clinical usefulness profile of our products, to develop short-, medium-, and long-term local and national plans, and to collaborate cross-functionally with a customer-centred focus.</li>
<li>Build strong scientific and peer relationships with key stakeholders and identified major institutions within the health care sector, as well as to liaise with office-based medical managers to ensure optimal delivery of scientific information to the medical and scientific community.</li>
<li>Act as a scientific ambassador for Novo Nordisk, ensuring that the profile of the company remains high amongst key stakeholders through establishing a peer-to-peer relationship based on scientific rigor and integrity.</li>
<li>Provide medical training for various internal and external stakeholders.</li></ul><br>
<div></div>
<div>
The role demands spending more than 80% of the time in the field, with travelling flexibility.</div><br>
<div></div>
<div><b>
Your New Department</b></div>
<div>
The Clinical, Medical, Regulatory (CMR) department provides timely, accurate, and updated services to support Novo Nordisk in all therapeutic areas. The Clinical, Medical, Regulatory Department is a team of skilled and committed specialists within medical, clinical, regulatory, areas.</div><br>
<div></div>
<div><b>
Your Skills &amp; Qualifications</b></div>
<div>
You should have a strong medical background with qualifications as having degree in Medicine, and preferably with a post-graduate medical qualification. It is expected to have excellent command of written and spoken English and Turkish. Minimum of 2 years&rsquo; experience in medical affairs in the pharmaceutical industry is considered an advantage. The further sought skills are</div><br>
<div></div>
<ul>
<li>You have a critical thinking mindset to aim for the best qualitative solutions in a changing business environment with scientific and business integration mindset</li>
<li>You poss a strong scientific and have medical knowledge with a good business understanding with learning agility</li>
<li>You have an excellent communication and stakeholder management abilities and effective time management skills</li>
<li>You should be aligned with our Novo Nordisk Way and demonstrate knowledge of the health care system in Turkey and be able to link scientific data with business strategy</li></ul><br>
<div></div>
<div><b>
Working at Novo Nordisk</b></div>
<div>
At Novo Nordisk, we don&rsquo;t wait for change. We drive it. We&rsquo;re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales &ndash; we&rsquo;re all working to move the needle on patient care.</div><br>
<div></div>
<div><b>
What We Offer</b></div>
<div>
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.</div><br>
<div><b>
Deadline</b></div>
<div>
Apply before 4 November 2025. Applications are reviewed on an ongoing basis</div><div></div><div><br>
Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.</div></div></div></div></div></div>

Regional Medical Manager

Michael Page

<div>
 <p>
  Join a leading global pharmaceutical company as a Medical Strategy &amp; Field Excellence Lead for Neurology &amp; Rare Diseases.
 </p>
 <p>
  This senior role offers the opportunity to shape scientific direction, mentor regional teams, and drive impactful patient centered initiatives.
 </p>
 <p>
  <strong>
   Client Details
  </strong>
 </p>
 <p>
  Our client is a prestigious multinational pharmaceutical company with a strong heritage in specialty care and a growing focus on Neurology and Rare Diseases.
 </p>
 <p>
  <strong>
   Description
  </strong>
 </p>
 <p>
  * Develop and implement medical strategies and scientific content across the Neurology &amp; Rare Diseases portfolio
  <br/>
  * Design and deliver educational programs for internal medical teams and scientific partners
  <br/>
  * Provide mentorship, guidance, and capability development for regional medical staff
  <br/>
  * Represent the local organization in cross-country projects and global initiatives
  <br/>
  * Build and sustain relationships with key opinion leaders at national and regional levels
  <br/>
  * Drive strategic alignment between medical affairs and broader business objectives
  <br/>
  * Support access and value-based initiatives through data-driven medical insights
 </p>
 <p>
  <strong>
   Profile
  </strong>
 </p>
 <p>
  * Medical Doctor (MD) degree is a must.
  <br/>
  * Minimum 10 years of experience in medical affairs within the pharmaceutical industry.
  <br/>
  * Solid background in Neurology and/or Rare Diseases is a strong advantage.
  <br/>
  * Proven leadership and mentoring experience within medical teams.
  <br/>
  * Demonstrated ability to build effective cross-functional collaboration with marketing, market access, and commercial functions.
  <br/>
  * Strategic mindset with strong analytical and scientific interpretation skills.
  <br/>
  * Excellent communication and presentation skills in both written and spoken English.
  <br/>
  * Ability to engage and maintain long-term relationships with national and regional key opinion leaders.
  <br/>
  * High level of accountability, adaptability, and initiative in a fast-changing environment.
  <br/>
  * Willingness to work in a dynamic, innovation-driven organization focused on patient value.
 </p>
 <p>
  <strong>
   Job Offer
  </strong>
 </p>
 <p>
  This is a unique opportunity to take on a regional leadership role in one of the most innovative and reputable pharmaceutical organizations.
 </p>
</div>


Scientific Lead - Neurology and Rare Diseases

Boehringer Ingelheim

<div><p>We are looking for a <b>Medical Advisor </b>to join our medical affairs team, for Specialty and Rare Diseases therapeutic area, based in <b>&#304;stanbul, T&uuml;rkiye </b>. 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.<br>
</p><p><br>
This position reports to the Medical Affairs Manager.<br>
<br>
<br>
<br>
<b>Responsibilities
</b></p><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.<br>
<li>
</li></ul><p></p><p><b>Requirements
</b></p><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<br>
<li>
</li></ul><p></p><p><b>What happens Next?
</b></p><p>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.
<br>
<br>
<b>SPL Screening:
</b></p><p>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.</p></div><p></p>

Medical Advisor

ARVEN CONSULTANCY

<div>
 <p>
  <strong>
   Overview
  </strong>
 </p>
 <p>
  TheLifeCo Wellbeing is a global wellness brand offering holistic health and longevity programs at its international centers. The role involves ensuring the safe implementation of clinical therapies, conducting medical consultations, and performing well-aging applications in alignment with TheLifeCo philosophy.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   This role will be based in Bodrum but will act in rotation between different locations such as Egypt, Caribbean, Thailand, Antalya. If you like to travel, meet with different cultures and create an amazing experience for people - we should meet!
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Supervise clinical procedures such as IV therapies, colon hydrotherapy, stem cell, PRP, lipolysis, and exosome applications.
  </li>
  <li>
   Conduct medical consultations, review guest suitability for detox and fasting programs, and provide continuous health monitoring.
  </li>
  <li>
   Provide emergency medical support and coordinate with external medical partners when necessary.
  </li>
  <li>
   Collaborate with the wellness team (coaches, nurses, therapists, dietitians) for integrated guest care.
  </li>
  <li>
   Educate guests on preventive and holistic health principles.
  </li>
  <li>
   Contribute to standardization and development of medical wellness protocols across TheLifeCo centers.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements
  </strong>
 </p>
 <ul>
  <li>
   Medical degree (MD or equivalent) with valid license to practice
  </li>
  <li>
   Minimum 3&ndash;5 years of clinical experience (internal, family, or integrative medicine preferred)
  </li>
  <li>
   Strong interest or experience in detox, fasting, or plant-based nutrition
  </li>
  <li>
   Fluency in English; additional languages are a plus
  </li>
  <li>
   Excellent communication and teamwork skills
  </li>
  <li>
   Passion for holistic wellness and preventive medicine
  </li>
 </ul>
 <p>
 </p>
</div>


Medical Doctor (Wellness Focused)

Medtronic

<div><p>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
</p><p></p><h1 class="jobSectionHeader"><b>A Day in the Life
</b></h1><p><b>Careers That Change Lives
</b></p><p>Join a mission-driven industry leader in medical technology and solutions to help drive innovation and transform the healthcare landscape. As <b>Clinical Research &amp; Medical Sciences Director </b>you will oversee both clinical and medical sciences aspects of running the medical organization in the TuRMECA region. Reporting to Chief Medical Officer Global Regions and VP Clinical Research &amp; Medical Sciences, you will lead the development and execution of clinical research and medical sciences agenda in TuRMECA region to enable patient access to innovative medical technologies.
</p><p></p><p><b>A Day in Life
</b></p><ul><li>Provides Clinical/Medical Leadership at Business Reviews and discussions with the respective Country Leaders in the TuRMECA region.
</li><li>As a Leader within the TuRMECA regional organization, contributes to the development of a Clinical &amp; Medical affairs strategy and execute them in their sub-region.
</li><li>Is seen as the Voice of the Patient and the HCP.
</li><li>Provides Strategic Leadership for the development of Clinical strategy across OUs relevant to the region in Medtronic sponsored studies, Collaborative Research and ERPs including execution of Clinical Research and Medical Affairs.
</li><li>Ensures that the studies are scientifically valid and meet all relevant regulatory requirements and be conducted within ethical guidelines.
</li><li>Leads execution for both local and global studies, manages clinical research projects across Medtronic therapies across multiple businesses.
</li><li>Ensures that all clinical studies are published based on a fair assessment of the safety and efficacy of the tested product (s) and attainment of product approvals in a timely matter.
</li><li>Partners with the OUs/Marketing regionally to seek insights and disseminate the published data both globally and regionally. This may be done through Advisory Boards (ABs) to seek advice, Focus Group Discussions (FGDs), Continuing Medical Education (CMEs), Round Table Discussions (RTDs), and webinars for safe and effective use of our products.
</li><li>Partners with Regulatory to contribute and partnering to implement regulatory strategies to obtain timely product approvals form worldwide regulatory bodies.
</li><li>Develop the Healthcare Professional (HCPs) and Key Opinion Leaders network and lead a strategic partnership and engagement.
</li><li>Develops and maintains a deep knowledge and understanding of the science behind our products and is seen as an internal expert. To also act as a Speaker in scientific meetings as the voice of the company.
</li><li>Responsible for the governance and compliance within the region. Ensures that all activities are executed as per the Medtronic Business Code of Conduct and local laws and regulations.
</li><li>Utilizes advanced subject matter expertise to provide medical input to various functions (General Management, Global Strategy &amp; Portfolio Management, Business Development &amp; Licensing, Research &amp; Development, &amp; Marketing) and Organizational Units to facilitate insightful decision-making and enable achievement of business objectives.
</li><li>Ensures effective objective value propositions are developed and articulated for Medtronic technologies to stakeholders (patients, health care providers, payers, government agencies, health technology assessment organizations, public) through appropriate channels.
</li><li>Responsible to interpret clinical trials/research, establishes and approves scientific methods for design and implementation of clinical protocols, and final reports.
</li><li>Proactively develops current competitive intelligence in our product space.
</li><li>Represents Medtronic from Clinical Research and Medical Sciences perspective within the region and collects feedback from local customers and authorities.
</li><li>Builds and maintains a strong network and close relationship with the various internal and external parties
</li></ul><p></p><p><b>Qualifications/ must have
</b></p><ul><li>10 years of relevant experience within clinical research &amp; medical sciences with 7+ years of managerial experience, or advanced degree with a minimum of 8 years of relevant experience with 7+ years of managerial experience.
</li><li>University degree &ndash; medical or scientific discipline.
</li><li>Proven strategic thinking, stakeholder management, and team leadership.
</li><li>Fluent in English and local language.
</li><li>Strong communication and networking skills.
</li></ul><p></p><p><b>Nice to have
</b></p><ul><li>Experience in international and cross-functional environments preferred
</li></ul><p></p><p>To be successful in this role you must be an excellent communicator, able to drive change by influence (internally as well as externally) and have strong managerial skills/experience.
</p><p></p><p><b>Physical Job Requirements
</b><br>
<br>
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
</p><p></p><h1 class="jobSectionHeader"><b>Benefits &amp; Compensation
</b></h1><p><b>Medtronic offers a competitive Salary and flexible Benefits Package
</b><br>
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.<br>
<br>
</p>This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
<p></p>This position is eligible for an annual long-term incentive plan.
<p></p><h1 class="jobSectionHeader"><b>About Medtronic
</b></h1><p>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
<br>
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
<br>
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</p></div><p></p>

TuRMECA Clinical Research and Medical Science Director

DEVA Holding A.Ş.

<div>
 <p>
  <strong>
   QUALIFICATIONS
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  DEVA has been operating since 1958 and is one of the pioneering pharmaceutical companies in Turkey. DEVA, having R&amp;D in focus, manufactures with international quality standards and currently exports products to other countries worldwide.
 </p>
 <p>
  <br/>
 </p>
 <p>
  DEVA is seeking for a
  <strong>
   Medical Manager
  </strong>
  ;
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; University degree in Medicine, Dentistry, Pharmacy, Veterinary,
 </p>
 <p>
  &bull; Must have been completed obligatory service as Doctor for new Medicine graduaters,
 </p>
 <p>
  &bull; Preferably 1 year experience in Medical Department,
 </p>
 <p>
  &bull; Excellent command of both written and spoken
  <strong>
   English &amp; German
  </strong>
  ,
 </p>
 <p>
  &bull; Computer literacy, good knowledge of MS Office tools,
 </p>
 <p>
  &bull; Excellent interpersonal, communication and presentation skills,
 </p>
 <p>
  &bull; Result oriented in a competitive business environment,
 </p>
 <p>
  &bull; Valid driver&rsquo;s licence,
 </p>
 <p>
  &bull; No restrictions for travel domestically and internationally,
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   JOB DESCRIPTION
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; Providing medical support to the development and marketing of products,
 </p>
 <p>
  &bull; Providing internal medical training activities for sales force; preparing and reviewing all training manuals and visual materials,
 </p>
 <p>
  &bull; Actively search for new data, literature, guidelines to provide updated medical background for medico-marketing activities,
 </p>
 <p>
  <br/>
 </p>
 <p>
  <em>
   Bir &ccedil;al&inodot;&scedil;an aday&inodot; olarak, sizinle aram&inodot;zdaki t&uuml;m ileti&scedil;imde bilgilerinizi 6698 say&inodot;l&inodot; Ki&scedil;isel Verilerin Korunmas&inodot; Kanunu&rsquo;na, yasal mevzuata ve Ki&scedil;isel Verileri Koruma Kurumu kararlar&inodot;na uygun olarak i&scedil;liyoruz. Detayl&inodot; bilgiye ve ayd&inodot;nlatma metnimize link &uuml;zerinden ula&scedil;abilirsiniz. https://www.deva.com.tr/tr/kvkk
  </em>
 </p>
</div>


Medical Manager

Explore 245+ Medical concultant in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey this November. Find roles across top companies and apply now to boost your career.