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clinical affairs manager

ulrich medical

<div><div>Angestellt (Vollzeit) - m / w / d</div>
<div></div><div>15.12.2025
</div><div>Job-Nummer: req289</div>
<div><p>Bei <b>ulrich medical</b> begeistern wir uns f&uuml;r die Gesundheit und die Lebensqualit&auml;t von Menschen. Teilen Sie unsere Leidenschaft f&uuml;r <i>Medizintechnik</i> und widmen Ihre Energie gerne der Entwicklung und Vermarktung innovativer Produkte? Dann kommen Sie zu ulrich medical. Es erwartet Sie ein Unternehmen, in dem der Mensch im Mittelpunkt steht und Teamgeist gelebt wird, ein dynamisches Umfeld mit vielen M&ouml;glichkeiten sich beruflich und pers&ouml;nlich weiterzuentwickeln.</p>
</div><p></p><div><h2 class="jobSectionHeader"><b>Hier sind Sie gefragt</b></h2>
<ul><li>Sie erstellen eigenst&auml;ndig klinische Bewertungen (CEP/CER) inklusive der dazu notwendigen Recherchen (Literatur,
<br>
Beh&ouml;rdenmeldungen etc.) sowie SSCPs</li><li>
Sie fertigen selbst&auml;ndig PMS/PMCF-Pl&auml;ne und die dazu geh&ouml;rigen Berichte (PMCF-Bericht, PMS-Bericht, PSUR) an</li><li>
Sie arbeiten eng mit externen Dienstleistern zusammen (Statistikern, Klinischen Beratern, etc.)</li><li>
Sie betreuen die wissenschaftliche Begleitung unserer Produkte als Schnittstelle zwischen Kliniken, &Auml;rzten, Vertrieb,
<br>
Entwicklung, Produktmanagement, Risikomanagement und Marketing</li><li>
Sie vermitteln und verfolgen die Einhaltung der regulatorischen Anforderungen, inkl. deren &Auml;nderungen</li><li>
Sie aktualisieren dazugeh&ouml;rige Prozesse aufgrund regulatorischer &Auml;nderungen und optimieren diese im Sinne des Lean Managements</li><li>
Sie stellen klinische Daten und Bewertungen f&uuml;r internationale Zulassungen bereit</li><li>
Sie unterst&uuml;tzen bei der Planung und Betreuung klinischer Studien und werten diese mit aus</li></ul>
</div><p></p><div><h2 class="jobSectionHeader"><b>Das bringen Sie mit</b></h2>
<ul><li>Sie haben ein medizinisches, naturwissenschaftliches oder technisches Studium erfolgreich abgeschlossen oder verf&uuml;gen &uuml;ber eine vergleichbare Qualifikation mit entsprechenden Zusatzqualifikationen</li><li>
Sie bringen fundierte Kenntnisse bez&uuml;glich der gesetzlichen und regulatorischen Vorgaben im Bereich der Durchf&uuml;hrung, Interpretation und Publikation von wissenschaftlichen Studien im medizinischen Umfeld mit</li><li>
Zudem verf&uuml;gen Sie &uuml;ber 3-5 Jahre Berufserfahrung und kennen sich mit Medizinprodukten aus, aber auch ambitionierten Berufseinsteigern geben wir eine Chance</li><li>
Neben profunden Statistikkenntnissen &uuml;berzeugen Sie durch Ihre analytischen F&auml;higkeiten</li><li>
Sie bringen sehr gute Englischkenntnisse mit und sind im Umgang mit dem Office Paket sicher</li><li>
Sie runden Ihr Profil durch die F&auml;higkeit ab, Probleme wahrzunehmen, strukturiert L&ouml;sungen zu erarbeiten und komplexe Sachverhalte in interdisziplin&auml;ren Teams verst&auml;ndlich zu vermitteln</li></ul>
</div><p></p><div><h2 class="jobSectionHeader"><b>Das bieten wir Ihnen</b></h2>
<p>Freuen Sie sich &uuml;ber einen zukunftssicheren Arbeitsplatz an einem modernen Standort mit attraktiver Verg&uuml;tung. Als familienfreundliches <b>Unternehmen</b> legen wir Wert darauf, dass Sie Ihre beruflichen und privaten Ziele vereinbaren k&ouml;nnen und sich im Unternehmen wohlf&uuml;hlen. Dies unterst&uuml;tzen wir neben flexibler Arbeitszeitgestaltung durch vielf&auml;ltige Sozialleistungen, gesunde Verpflegung und Events abseits des Arbeitsalltags.</p>
</div><div><div><div><div><h2 class="jobSectionHeader"><b>Wir haben Ihr Interesse geweckt?</b></h2>
<div>Dann w&uuml;rden wir Sie gerne kennenlernen! Bewerben Sie sich einfach und komfortabel direkt &uuml;ber unser Online-Bewerbungsformular.</div></div></div></div></div></div>

Clinical Affairs Manager

IMPETUS EXECUTIVE

<div>
 <p>
  We are looking for a proactive and experienced
  <strong>
   Administrative Affairs Manager
  </strong>
  to oversee all general services and office operations within our holding structure. Reporting directly to the CFO, this role will ensure the smooth functioning of administrative processes, facility services, vendor management, and workplace efficiency across our group headquarters and relevant subsidiaries.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Manage and supervise all administrative operations including office management, facility services, reception, security, cleaning, catering, and logistics,
  </li>
  <li>
   Ensure proper functioning and maintenance of office infrastructure and building services,
  </li>
  <li>
   Oversee vendor management, service contracts, and procurement processes related to administrative needs,
  </li>
  <li>
   Support executive management with protocol services, meeting arrangements, and company-wide coordination efforts,
  </li>
  <li>
   Lead cost control and budget planning for general administrative expenses,
  </li>
  <li>
   Ensure compliance with local regulations, health &amp; safety standards, and internal company policies,
  </li>
  <li>
   Coordinate with HR, Finance, and IT departments to ensure crossfunctional operational efficiency,
  </li>
  <li>
   Manage office renovation, relocation, and workplace improvement projects as needed,
  </li>
  <li>
   Act as the main point of contact for outsourced service providers and corporate building management.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications &amp; Experience
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Business Administration, Facility Management, or a related field,
  </li>
  <li>
   Minimum 7&ndash;10 years of experience in administrative affairs or office management, preferably in a holding, multinational, or corporate environment,
  </li>
  <li>
   Strong understanding of general services, procurement, contract management, and workplace operations,
  </li>
  <li>
   Experience managing third-party vendors and service providers,
  </li>
  <li>
   Good knowledge of local legal requirements and occupational health &amp; safety standards,
  </li>
  <li>
   Excellent organizational, negotiation, and communication skills,
  </li>
  <li>
   Proficiency in MS Office applications and administrative systems,
  </li>
  <li>
   Fluency in English (written and spoken),
  </li>
  <li>
   Strong sense of ownership, service mindset, and attention to detail.
  </li>
 </ul>
 <p>
 </p>
</div>


Administrative Manager

<div><div><div><div><div><div><b>Entity:</b> CSL Behring</div>
<div><b>Job Category:</b> Medical Affairs</div>
<div><b>Job Family:</b> Medical Science Advisor</div>
<div><b>Job Type:</b> Full Time</div>
<div><b>Location</b><b>:</b> Istanbul, Turkey</div>
<div><b>Employer Reference:</b> R-266948</div>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><div><b>Responsibilities:</b></div><ul><div><div>
Serves as CSL medical contact for both internal and external partners in interactions and communications requiring medical knowledge and medical expertise on CSL products and relevant therapeutic areas.</div></div><div><div>
Supports medical affairs operations on planning and implementation of projects.</div></div><div><div>
Serves as medical expert and contributes to strategic product planning for the region/country.</div></div><div><div>
Implements strategy for scientific interactions with the medical community including key opinion leaders and patient advocacy groups.</div></div><div><div>
Engages with key thought-leaders, Health Care Professionals, regional / local institutions and organizations in the territory through appropriate high-level scientific interactions.</div></div><div><div>
Actively participates in the preparation of scientific, promotional and educational events in Turkey and provides medical expertise needed for preparing these events in adherence with CSL values and Code of Responsible Business Practice, local CSL processes, relevant local and international codes and regulations.</div></div><div><div>
Ensures internal training and continuous medical support for the cross functional teams.</div></div><div><div>
Coordinates the review of Investigator Initiated Research (IIR) study proposals.</div></div></ul><div></div><div><b>
Qualifications:</b></div><ul><div><div>
University degree in Medicine or Pharmacy</div></div><div><div>
Minimum 2 years of experience in the Medical Affairs is preferred</div></div><div><div>
Fluent in English (both verbal and written)</div></div><div><div>
Good planning and organizational skills</div></div><div><div>
Advanced interpersonal, project management and presentation skills</div></div><div><div>
Ability to form strong communication networks with key internal and external stakeholders</div></div><div><div>
Ability to 'translate' scientific data into meaningful, clear and compliant content for stakeholder communications and engagement</div></div><div><div>
General clinical trial experience is preferred</div></div><div><div>
Ethical and principle based approach to decision-making</div></div><div><div>
Valid driver's license</div></div><div><div>
No restrictions for travel domestically and internationally</div></div></ul></div><div></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div>
<div>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</div>
<div>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</div>
<div>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</div>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div>
<div>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</div>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div>
<div>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</div>
<div>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</div>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div>
<div>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</div>
</div>
<h2 class="jobSectionHeader"><b>Location</b></h2>
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Medical Advisor

Roche

<div><p>Bei Roche kannst du ganz du selbst sein und wirst f&uuml;r deine einzigartigen Qualit&auml;ten gesch&auml;tzt. Unsere Kultur f&ouml;rdert pers&ouml;nlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du f&uuml;r das, was du bist, wertgesch&auml;tzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl pers&ouml;nlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und in Zukunft. Werde Teil von Roche, wo jede Stimme z&auml;hlt.</p><div></div><div>
Die Position</div><p>
Medical Lead is the key Medical Affairs role that develops broad medical &amp; scientific expertise within given Disease/Therapeutic Areas. As a Medical Lead, you support development and execution of patient-focused medical strategies, primarily drive scientific exchange and evidence generation activities.</p><p></p><p><b>
Key Responsibilities</b></p><ul><li><p>
You are a strategic partner who provides medical insights and expertise to the organisation and executes all planned medical activities.</p></li><li><p>
You will be the medical responsible of the team and will be more in the field.</p></li><li><p>
You manage the integrity and accuracy of scientific and medical data communicated internally and externally for promotional and non-promotional purposes.</p></li><li><p>
You collaborate with stakeholders in identifying and prioritising relevant research ideas and developing them into research projects.</p></li><li><p>
You collaborate closely with Clinical Operations across different phases of interventional clinical trials: Gaining clarity and communicating/spreading the knowledge to communities of interest, helping to define and maintain country participation strategy, supporting development of sites selection strategy through a disease area lens by different means including participation in site feasibility activities, pre-activation site visits and other F2F and remote interactions with the sites as needed, patient recruitment &amp; retention, protocol &amp; patient-related issues, scientific communication of study results, clinical study report and scientific publications.</p></li><li><p>
You detect the medical gap/need for RWD/E generation activities by reviewing Integrated Evidence Plans, communicate, agree and document, plan &amp; execute and/or participate in respective work in non-interventional studies and RWD/E generation activities: Definition of the research questions and study objectives, study design and protocol, study budget, feasibility, site selection, pre-activation and ad-hoc visits, patient recruitment, protocol &amp; patient issues, scientific communication of study results, clinical study report and scientific publications.</p></li></ul><p></p><p><b>
Who You Are</b></p><ul><li><p>
You have Medicine, pharmacy or dentistry degree</p></li><li><p>
Your experience in Oncology is preferred</p></li><li><p>
You have previous experience in Pharma Industry</p></li><li><p>
You are fluent in Turkish and English</p></li><li><p>
You have strategic thinking and growth mindset</p></li><li><p>
You are collaborative and experienced in stakeholder management</p></li></ul><p></p><div><br>
Wer wir sind</div><p>
Eine ges&uuml;ndere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und f&uuml;r zuk&uuml;nftige Generationen. Durch unser Engagement werden &uuml;ber 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgef&uuml;hrt. Wir ermutigen uns gegenseitig, neue M&ouml;glichkeiten zu erkunden, Kreativit&auml;t zu f&ouml;rdern und hohe Ziele zu setzen, um lebensver&auml;ndernde Gesundheitsl&ouml;sungen zu liefern.</p><p></p><p>
Gemeinsam k&ouml;nnen wir eine ges&uuml;ndere Zukunft gestalten.</p><p></p><p><b>
Roche ist ein Arbeitgeber, der die Chancengleichheit f&ouml;rdert.</b></p></div>

Oncology Medical Lead

HUMAN KAPİTAL İNSAN KAYNAKLARI

<div><div>S&uuml;rekli / Tam Zamanlı</div>
<div></div><div><b>Referans Numarası :</b> 1981-2041-2025
</div><div>İşe Alınacak Kişi Sayısı : 1</div>
<div></div><div><p>T&uuml;rkiye - İstanbul (Asya)
</p></div>
<div></div><div><p><b>Pozisyon Seviyesi : </b>:Orta D&uuml;zey Y&ouml;netici</p>
</div><div></div><div><p><b>İş Alanı : </b>: Ruhsatlandırma</p>
</div><div><div><h4 class="jobSectionHeader"><b>Genel Nitelikler ve İş Tanımı :</b></h4>
</div><div><p>As <b>Human Kapital</b>, on behalf of our corporate client operating in the pharmaceutical industry, we are seeking an <b>International Regulatory Affairs Manager</b> with strong experience in overseas regulatory processes, solid knowledge of global regulations, and proven team management capabilities.</p><p></p><p><b>
Required Qualifications</b></p><ul><li>
Bachelor&rsquo;s degree in Pharmacy, Chemical Engineering, Chemistry, or a related field,</li><li>
Minimum 10 years of experience in the pharmaceutical industry,</li><li>
Prior experience in team management with demonstrated leadership skills,</li><li>
Preferably experienced in preparing overseas regulatory submission dossiers in <b>CTD format</b>,</li><li>
Strong knowledge of global regulations and international health authorities,</li><li>
Familiar with technology transfer processes and <b>R&amp;D (Product Development)</b> activities,</li><li>
Advanced level of English,</li><li>
Proficient in MS Office applications,</li><li>
Strong communication skills and a collaborative team player,</li><li>
For male candidates, completion of military service,</li></ul><p>
Able to reside in <b>Istanbul Ataşehir&ndash;Kadık&ouml;y</b> area or nearby districts.</p><p>
For Apply; https://humancapital.com.tr/ilan/143/international-regulatory-affairs-manager</p><p></p><p><b>
Duties and Responsibilities</b></p><ul><li>
Monitoring and implementing international regulatory requirements of relevant countries&rsquo; health authorities,</li><li>
Preparing overseas regulatory submission dossiers in compliance with country-specific requirements and managing the submission process,</li><li>
Following up all post-submission processes until product approval and ensuring internal coordination,</li><li>
Establishing effective communication with relevant health authorities,</li><li>
Preparing packaging mock-ups for products to be marketed abroad in accordance with the local language, and managing and tracking design approval processes,</li><li>
Notifying relevant country authorities of variations and changes made to licensed products,</li><li>
Tracking license renewal processes,</li><li>
Working in close cooperation with the Factory Quality Control unit,</li><li>
Contributing to R&amp;D processes,</li><li>
Following up variation approval processes,</li><li>
Managing and supervising the assigned team.</li></ul><p></p><p><b>
HUMAN KAPİTAL Human Resources and Consulting Services Industry and Trade Limited Company</b> is a private employment agency operating with the authorization of the Turkish Employment Agency dated <b>20.06.2025</b> and numbered <b>228</b>.<br>
In accordance with Law No. <b>4904</b> of the Turkish Employment Agency, no benefit of any kind may be obtained from job seekers.<br>
Charging job seekers any fee is strictly prohibited.</p>
</div></div><div><div><h4 class="jobSectionHeader"><b>Aday Kriterleri</b></h4>
</div><div><ul><li><b>İlan Tarihi : </b>15.12.2025</li>
<li><b>Eğitim Seviyesi: </b>Lisans Mezun, Y&uuml;ksek Lisans Mezun</li>
<li><b>Yaşadığı Şehir:</b> İstanbul (Asya),
</li><li><b>Tecr&uuml;be Yılı:</b> 10-0 Yıl</li>
<li><b>Yabancı dil ve seviyesi:</b> İngilizce - ( Seviye : İleri)<br>
</li><li><b>Askerlik Durumu:</b> Yapıldı, Muaf
</li><li><b>Firmanın Tercih Ettiği Sekt&ouml;rler :</b> İla&ccedil; &Uuml;retim ve Satışı</li></ul></div></div></div>

INTERNATIONAL REGULATORY AFFAIRS MANAGER

SEGULA Technologies

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 SEGULA Technologies is a globally leading engineering group with a presence in 30 countries, 140 locations, and a workforce of 12,000 employees. With 50 years of accumulated experience, the company is engaged in projects across various sectors, including Automotive, Defense, Aerospace, Rail Systems, and the Energy industry.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 The
 <strong>
  Business Development Manager
 </strong>
 position primarily covers engineering, software, systems, infrastructure, and digital transformation projects carried out within the field of
 <strong>
  Information Technology (IT)
 </strong>
 . Within this scope, customer needs analysis, resource planning, proposal preparation, and recruitment processes will be conducted.
 <br/>
 <br/>
 <ul>
  <li>
   Analyze the engineering and technical needs of existing customers,
  </li>
  <li>
   Identify the required personnel and other resources to meet these needs,
  </li>
  <li>
   Support assessment, evaluation, and recruitment processes in line with the required human resources,
  </li>
  <li>
   Work in close coordination with technical teams, Human Resources, and Administrative Affairs departments throughout these processes,
  </li>
  <li>
   Manage proposal processes as well as customer and personnel relationships,
  </li>
  <li>
   Ensure the continuation and development of existing and new business activities in line with company objectives, including the management of personnel and customer relationships,
  </li>
  <li>
   Take an active role in the corporate branding process,
  </li>
  <li>
   Report customer needs, resource requirements, proposals, and recruitment processes related to both existing and new customers to senior management.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree from an Engineering faculty,
  </li>
  <li>
   Preferably experienced in business development, sales, project management or similar roles within Information Technology (IT)&ndash;driven engineering, software, systems, infrastructure or digital transformation projects,
  </li>
  <li>
   Knowledgeable and experienced in customer needs analysis, resource planning, proposal preparation and contract management processes,
  </li>
  <li>
   Able to contribute to workforce planning, assessment and recruitment processes in line with IT competencies,
  </li>
  <li>
   Strong communication and organizational skills, with the ability to work in coordination with technical teams, Human Resources and Administrative Affairs departments,
  </li>
  <li>
   Experienced in customer relationship management, stakeholder communication and negotiation processes,
  </li>
  <li>
   Possessing strong analytical thinking skills, with proficiency in reporting and presenting to senior management,
  </li>
  <li>
   Capable of identifying new business opportunities and developing existing customer portfolios in line with company objectives,
  </li>
  <li>
   Willing to take an active role in corporate branding and company representation,
  </li>
  <li>
   Preferably with advanced level of English proficiency,
  </li>
  <li>
   No travel restrictions and able to adapt to a dynamic working environment.
  </li>
 </ul>
</div>


Business Development Manager

<div><b>Company Description</b><p><br>
SEGULA Technologies is a globally leading engineering group with a presence in 30 countries, 140 locations, and a workforce of 12,000 employees. With 50 years of accumulated experience, the company is engaged in projects across various sectors, including Automotive, Defense, Aerospace, Rail Systems, and the Energy industry.</p><b><br>
Job Description</b><p><br>
The <b>Business Development Manager</b> position primarily covers engineering, software, systems, infrastructure, and digital transformation projects carried out within the field of <b>Information Technology (IT)</b>. Within this scope, customer needs analysis, resource planning, proposal preparation, and recruitment processes will be conducted.</p><ul><li><p>
Analyze the engineering and technical needs of existing customers,</p></li><li><p>
Identify the required personnel and other resources to meet these needs,</p></li><li><p>
Support assessment, evaluation, and recruitment processes in line with the required human resources,</p></li><li><p>
Work in close coordination with technical teams, Human Resources, and Administrative Affairs departments throughout these processes,</p></li><li><p>
Manage proposal processes as well as customer and personnel relationships,</p></li><li><p>
Ensure the continuation and development of existing and new business activities in line with company objectives, including the management of personnel and customer relationships,</p></li><li><p>
Take an active role in the corporate branding process,</p></li><li><p>
Report customer needs, resource requirements, proposals, and recruitment processes related to both existing and new customers to senior management.</p></li></ul><b><br>
Qualifications</b><ul><li><p><br>
Bachelor&rsquo;s degree from an Engineering faculty,</p></li><li><p>
Preferably experienced in business development, sales, project management or similar roles within Information Technology (IT)&ndash;driven engineering, software, systems, infrastructure or digital transformation projects,</p></li><li><p>
Knowledgeable and experienced in customer needs analysis, resource planning, proposal preparation and contract management processes,</p></li><li><p>
Able to contribute to workforce planning, assessment and recruitment processes in line with IT competencies,</p></li><li><p>
Strong communication and organizational skills, with the ability to work in coordination with technical teams, Human Resources and Administrative Affairs departments,</p></li><li><p>
Experienced in customer relationship management, stakeholder communication and negotiation processes,</p></li><li><p>
Possessing strong analytical thinking skills, with proficiency in reporting and presenting to senior management,</p></li><li><p>
Capable of identifying new business opportunities and developing existing customer portfolios in line with company objectives,</p></li><li><p>
Willing to take an active role in corporate branding and company representation,</p></li><li><p>
Preferably with advanced level of English proficiency,</p></li><li><p>
No travel restrictions and able to adapt to a dynamic working environment.</p></li></ul></div>

Explore 346+ Clinical affairs manager in Istanbul Turkey this January. Find roles across top companies and apply now to boost your career.

346 clinical affairs manager jobs IN Istanbul Turkey

Clinical Affairs Manager

Administrative Manager

Medical Advisor

Oncology Medical Lead

INTERNATIONAL REGULATORY AFFAIRS MANAGER

Business Development Manager

Business Development Manager