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field medical manager - hematology Jobs in Istanbul

field medical manager - hematology

medical manager

medical science liaison

area manager, fulfilment center operations Jobs in Istanbul

area manager, fulfilment center operations

field medical manager hematology

Sanofi

<div>Job Title: Field Medical Manager - Hematology<ul><li>
Location: Istanbul</li></ul>
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>
University degree from Medicine (MD) or Pharmacy is required.</li><li>
Prior experience in the pharmaceutical industry and in Hematology is desired.</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 - Hematology

<div>
 
 
 Job Title:
 
 
 Field Medical Manager - Hematology
 
 
 <ul>
 <li>
 Location: Istanbul
 
 
 </li>
 </ul>
 
 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>
 University degree from Medicine (MD) or Pharmacy is required.
 </li>
 <li>
 Prior experience in the pharmaceutical industry and in Hematology is desired.
 </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
 
 Pursue
 
 
 Progress
 
 .
 
 Discover
 
 
 Extraordinary
 
 .
 
 
 Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what&rsquo;s never-been-done-before. You&rsquo;ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people&rsquo;s lives? Let&rsquo;s Pursue Progress and Discover Extraordinary &ndash; together.
 
 
 At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
</div>

IQVIA

<div>Job Overview
The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.
The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:
Essential Functions
Functions as project team member:
<ul><li>Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting.
</li><li>Ensures medical activities run according to GCP and operate with highest efficiency.
</li><li>Establishes and maintains a network of medical/scientific consultants, etc.
</li><li>Supervises and manages Medical Director activities.
</li></ul>Clinical Activities:
<ul><li>Interacts with clients regarding drug development programs, study design and protocol.
</li><li>Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
</li><li>Interacts in team approach to develop statistical and data management sections of the protocol.
</li><li>Reviews the final protocol for clinical, safety and efficacy variables.
</li><li>Provides project team training on protocol and/or therapeutic areas.
</li><li>Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
</li><li>Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators, and site staff and/or participation in teleconference and WebEx presentations.
</li><li>Presents protocol and/or safety reporting information at investigator meetings.
</li><li>Develops project medical monitoring plans as requested.
</li><li>Provides on call coverage for protocol queries and site support.
</li><li>Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
</li></ul>Safety Monitoring and SAE Reporting Activities:
<ul><li>Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
</li><li>Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs and follow-up on outstanding safety queries, interacts with sponsor and discusses safety issues with site as needed.
</li><li>Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
</li><li>In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
</li><li>Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
</li></ul>Data Activities:
<ul><li>Provides medical review of eCRFs for clinical accuracy.
</li><li>Provides medical review of data analysis plan.
</li><li>Reviews safety fields at case freeze for reconciliation (if needed).
</li><li>Works with data group to reconcile SAE events as needed.
</li><li>Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
</li><li>Reviews data tables, listings, and figures.
</li><li>Reviews and/or writes portions of final clinical study report.
</li></ul>DSMB/Adjudication Committee Activities:
<ul><li>May assist sponsor in choosing committee members.
</li><li>May serve as a non-voting member to convene and organize proceedings.
</li><li>May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
</li><li>May determine data flow with sponsor to ensure reporting accuracy.
</li><li>Can ensure DSMB feedback is given to sites for IRBs.
</li><li>All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
</li></ul>Business Development Activities:
<ul><li>Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
</li><li>Supports business development activities with proposal development and sales presentations.
</li><li>Participates in feasibility discussions relating to specific project proposals.
</li></ul>Special Projects:
<ul><li>Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
</li><li>Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
</li><li>Participate in a variety of team quality improvement efforts as necessary.
</li><li>Perform other related duties as assigned or requested by the Chief Medical Officer.
</li></ul>Qualifications
<ul><li>Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
</li><li>10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
</li><li>3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
</li><li>Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
</li><li>Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
</li><li>Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
</li><li>Excellent oral and written communications skills as well as interpersonal skills are essential.
</li></ul>Oncology / Hematology
<ul><li>Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
</li><li>Board Certified / Board Eligible: Oncology (Required)
</li></ul>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</div>

Medical Director - Oncology , Home- Based

<div>Job Title: Field Medical Manager - Immunology/Respiratory
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>
University degree from medicine or pharmacy is required.</li><li>
Prior experience in the pharmaceutical industry and in Immunology is desired.</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><li>
Driver's license is a must.</li></ul>
null</div>

Field Medical Manager - Immunology/Respiratory

<div>
 
 
 Job Title:
 
 
 Field Medical Manager - Immunology/Respiratory
 
 
 
 
 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>
 University degree from medicine or pharmacy is required.
 </li>
 <li>
 Prior experience in the pharmaceutical industry and in Immunology is desired.
 </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>
 <li>
 Driver's license is a must.
 
 
 </li>
 </ul>
 null
 
 Pursue
 
 
 Progress
 
 .
 
 Discover
 
 
 Extraordinary
 
 .
 
 
 Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what&rsquo;s never-been-done-before. You&rsquo;ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people&rsquo;s lives? Let&rsquo;s Pursue Progress and Discover Extraordinary &ndash; together.
 
 
 At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
</div>

Medical Science Liaison

Kedrion Biopharma

<div>
 
 Kedrion Biopharma is a biopharmaceutical company specializing in the development, production and distribution of plasma-derived products. Kedrion has been producing plasma products for over 40 years and has a market presence in about 100 countries. Our employees are committed to the highest standards and therapies for the patients and clinicians in haematology, immunology, neurology, and transfusion medicine.
 
 
 
 
 
 We're looking for a
 
 Scientific Services Manager,
 
 to join our team in Istanbul or Ankara.
 
 
 
 
 
 
 Role Purpose:
 
 
 
 Scientific Service is the Responsible Person in charge of information on medicines which the Company puts on the market. Serves as technical and scientific reference, providing accurate, timely, fair-balanced medical information internally within Company and to external customers.
 
 
 He/She is responsible for fulfilling requirements for the Scientific Service role, according to the EU Directive 2001/83/EC in general and the local laws.
 
 
 
 
 
 
 Main Responsibilities:
 
 
 
 
 
 <ul>
 <li>
 Compiling and collating all information received from any source concerning the medicines that the Company puts on the market.
 </li>
 <li>
 Ensuring that product advertisements correspond to the content of the current effective marketing authorization/registration and comply with Turkey legal requirements for advertising and promotion, as well as Company procedures and policies.
 </li>
 <li>
 Ensuring that regulations on advertising &amp; promotion, external communication and interaction with healthcare professionals by the Company sales representatives are promptly implemented.
 </li>
 <li>
 Manages unsolicited requests for medical information from external customers (including product requests for unlicensed products in Turkey), in alignment with international best practices and Company policies and procedures.
 </li>
 <li>
 Reviews and approves evidence-based, balanced Medical Response Documents (MRDs) such as Standard Response Letters (SLRs) and Frequently Asked Questions (FAQs) dedicated to Turkey, ensuring compliance with local regulations.
 </li>
 <li>
 Reviews and approves Summary of Products Characteristics (SmPC) for products commercialized in the Country.
 </li>
 <li>
 Ensures records of medical inquiries, advertising &amp; promotion review/approval process, sales representatives training, in compliance with applicable regulations, Company policies and procedures.
 </li>
 <li>
 Maintains global interactions, mainly with Italy, relating to compliance with regulations for advertising &amp; promotion, therapeutic and medical information, and reporting activities.
 </li>
 <li>
 Responsible for setting up local procedures for the management of medical and scientific activities (Medical Inquiries Management, Promotional Material review, Scientific Training Management, etc.).
 </li>
 <li>
 Responsible for providing information and assistance to Regulatory Authorities, and for ensuring the decisions taken by the authorities or bodies responsible for monitoring advertising of medicinal products are immediately and fully complied with.
 </li>
 </ul>
 
 
 
 
 
 Requirements:
 
 
 
 
 
 <ul>
 <li>
 Professional experience in related fields of at least two years.
 </li>
 <li>
 Professional experience in quality management in pharmaceutical industry.
 </li>
 <li>
 Written and spoken fluency in Turkish and English.
 </li>
 <li>
 Education: university studies degree in the field of pharmacy
 </li>
 <li>
 Place of residence: Turkey
 </li>
 </ul>
</div>

Scientific Services Manager

Global Mission Support Services LLC

We're Hiring: Hospital General Manager &ndash; Nauru Deployment Location: Republic of Nauru (Full-time, On-site Deployment) Sector: Healthcare Management / Hospital Administration Contract: 6&ndash;12 monthsAbout the RoleWe are seeking a results-driven and experienced Hospital General Manager to oversee the operations of our hospital facility in Nauru. This is a leadership role that combines strategic direction, team management, and operational excellence to ensure the delivery of safe, high-quality patient care in a unique and challenging healthcare environment.Key Responsibilities<ul><li>Provide overall leadership and strategic direction for hospital operations</li><li>Oversee daily management of clinical and non-clinical departments</li><li>Manage personnel, resources, budgets, and supply chains effectively</li><li>Ensure compliance with healthcare regulations, policies, and standards</li><li>Collaborate with medical leadership and government stakeholders</li><li>Drive continuous quality improvement, patient safety, and performance outcomes</li><li>Lead risk management and emergency preparedness planning</li><li>Support staff development and foster a positive, productive work environment</li></ul>Qualifications and Experience<ul><li>Proven senior management experience in hospital or healthcare administration (e.g., COO, Hospital Director)</li><li>Minimum 6 years of healthcare leadership experience, including staff supervision and budget management</li><li>Strong knowledge of hospital operations, quality control, and accreditation standards</li><li>Bachelor&rsquo;s degree in Healthcare Administration, Business, or related field (Master&rsquo;s preferred)</li><li>Excellent leadership, organizational, and communication skills</li><li>Experience working in remote, island, or resource-limited healthcare settings is highly desirable</li></ul>What We Offer<ul><li>Competitive salary (commensurate with experience)</li><li>Free on-site housing and meals</li><li>30 days paid annual leave</li><li>Round-trip international airfare</li><li>Unique opportunity to lead and improve healthcare delivery in Nauru</li></ul>Interested Applicants may apply and send CV to talent@gmss.ltdJob Type: Full-timeApplication Question(s):<ul><li>Are you willing to be relocated to Nauru once we hire you?</li></ul>

Hospital General Manager- Nauru Deployment

Explore 603+ Field medical manager hematology in Istanbul this October. Find roles across top companies and apply now to boost your career.

603 field medical manager hematology jobs IN Istanbul

Field Medical Manager - Hematology

Field Medical Manager - Hematology

Medical Director - Oncology , Home- Based

Field Medical Manager - Immunology/Respiratory

Medical Science Liaison

Scientific Services Manager

Hospital General Manager- Nauru Deployment