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chief information security officer

Kalentas

<div>
 
 
 Job Overview:
 
 
 
 Responsible for developing and executing enterprise information security strategies that comply with Turkish laws and regulations (such as KVKK and Law No. 5651 on Internet), ensuring data privacy, network security, and business continuity. Lead responses to localized cyber threats and regulatory compliance requirements in Turkey.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Ensure that company operations comply with the Turkish Personal Data Protection Law (KVKK), data protection regulations in electronic communications, and cybersecurity directives for the financial industry.
 </li>
 <li>
 Regularly submit compliance reports to the Turkish Personal Data Protection Authority (KVKK Kurumu).
 </li>
 <li>
 Identify Turkey-specific cyber threats (e.g., APT attacks targeting financial infrastructure).
 </li>
 <li>
 Implement an Information Security Management System (ISMS) that meets Turkish Standard (TS 13613).
 </li>
 <li>
 nterface with regulatory bodies such as the Banking Regulation and Supervision Agency (BDDK) and the Capital Markets Board (SPK).
 </li>
 <li>
 Train local teams to understand the Turkish cybersecurity culture and legal environment.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 
 
 Required
 
 
 <ul>
 <li>
 Bachelor's degree or higher in Computer Science/Information Security.
 </li>
 <li>
 Over 3 years of experience in information security management.
 </li>
 </ul>
 
 
 Preferred
 
 
 <ul>
 <li>
 Experience with security projects in Turkish government or financial institutions.
 </li>
 <li>
 Familiarity with the Turkish Digital Signature (E-&Idot;mza) system integration.
 </li>
 <li>
 Understanding of Turkish cybersecurity incident response standards (BTK Y&ouml;nergesi).
 </li>
 </ul>
</div>

Chief Information Security Officer

KoçSistem

<div>
 
 T&uuml;rkiye&rsquo;nin k&ouml;kl&uuml; ve lider bilgi teknolojileri &scedil;irketi Ko&ccedil;Sistem&rsquo;de Gelece&gbreve;i Ke&scedil;fetmeye haz&inodot;r m&inodot;s&inodot;n? 80 y&inodot;l&inodot; a&scedil;k&inodot;n s&uuml;redir teknolojiyi i&scedil; d&uuml;nyas&inodot;n&inodot;n hizmetine sunan Ko&ccedil;Sistem, yenilik&ccedil;i &uuml;r&uuml;n ve servisleriyle &scedil;irketlere rekabet avantaj&inodot; ve verimlilik kazand&inodot;r&inodot;p, vizyonu, i&scedil; yap&inodot;&scedil; &scedil;ekli, payda&scedil;lar&inodot;na verdi&gbreve;i de&gbreve;er ile sekt&ouml;r&uuml;nde liderli&gbreve;ini s&uuml;rd&uuml;rmektedir.
 
 
 
 
 
 Bilgi G&uuml;venli&gbreve;i ekibimiz de birlikte &ccedil;al&inodot;&scedil;mak &uuml;zere
 
 &ldquo;Bilgi G&uuml;venli&gbreve;i Lideri"
 
 ar&inodot;yoruz.
 
 
 
 
 
 
 Genel Nitelikler
 
 
 <ul>
 <li>
 &Uuml;niversitelerin ilgili m&uuml;hendislik, matematik vb. b&ouml;l&uuml;mlerinde lisans ya da y&uuml;ksek lisans e&gbreve;itimini tamamlam&inodot;&scedil;,
 </li>
 <li>
 Min 7+ y&inodot;l profesyonel i&scedil; tecr&uuml;besi olan,
 </li>
 <li>
 Yeni teknolojiler &ouml;&gbreve;renmeye a&ccedil;&inodot;k, bilgisini s&uuml;rekli olarak g&uuml;ncel tutabilen,
 </li>
 <li>
 Karar alabilen, inisiyatif kullanabilen, i&scedil;birli&gbreve;i kurabilen ve kurumsal s&uuml;re&ccedil;lere uyumlu olan,
 </li>
 <li>
 ITIL 4, Cobit, ISO 20000, ISO 27001 gibi &ccedil;er&ccedil;eve ve standartlar hakk&inodot;nda bilgi sahibi ve tercihen sertifikal&inodot;,
 </li>
 <li>
 Teknik konularda liderlik yapabilecek,
 </li>
 <li>
 &Idot;yi derecede &Idot;ngilizce bilen,
 </li>
 <li>
 Analitik d&uuml;&scedil;&uuml;nebilme, problem &ccedil;&ouml;zme, planlama ve takip becerisi olan yeni bir tak&inodot;m arkada&scedil;&inodot; ar&inodot;yoruz.
 </li>
 </ul>
 
 
 
 
 
 &Idot;&scedil; Tan&inodot;m&inodot;
 
 
 <ul>
 <li>
 Bilgi G&uuml;venli&gbreve;i Stratejilerini olu&scedil;turmak, y&ouml;netmek ve raporlamak,
 </li>
 <li>
 BT G&uuml;venlik vaka y&ouml;netiminde tespit, idare ve m&uuml;dahale alanlar&inodot;ndan sorumlu olacak,
 </li>
 <li>
 Bilgi G&uuml;venli&gbreve;i ve Risk Y&ouml;netimi ile ilgili Politika ve Prosed&uuml;rlerin takibini ve g&uuml;ncelli&gbreve;ini sa&gbreve;layacak,
 </li>
 <li>
 &Idot;&ccedil; ve D&inodot;&scedil; denetim (Holding BT, ISO standartlar&inodot;, PCI DSS vb.) isterleri sa&gbreve;lamak ve takip ad&inodot;na ilgili ekipler ile koordinasyonundan sorumlu olacak,
 </li>
 <li>
 Bilgi G&uuml;venli&gbreve;i ve Risk Y&ouml;netimi kurum stratejileri ile ilgili payda&scedil;larla gerekli hizalanmay&inodot; sa&gbreve;layacak,
 </li>
 <li>
 &Scedil;irketin Bilgi G&uuml;venli&gbreve;i, Risk Y&ouml;netimi, &Idot;&ccedil; Denetim, M&uuml;&scedil;teri Denetimi Koordinasyonu, &Idot;&scedil; S&uuml;reklili&gbreve;i &ccedil;al&inodot;&scedil;malar&inodot;n&inodot;n takibi ve y&ouml;nlendirilmesini ger&ccedil;ekle&scedil;tirecek,
 </li>
 <li>
 Sistem ve G&uuml;venlik birimlerinin ortak KPI'lar&inodot;n&inodot; takip edilerek raporlayacak,
 </li>
 <li>
 Kurum i&ccedil;i &ccedil;al&inodot;&scedil;anlar ad&inodot;na Bilgi G&uuml;venli&gbreve;i Fark&inodot;ndal&inodot;k Program&inodot;n&inodot; i&scedil;letecek,
 </li>
 <li>
 Geli&scedil;tirilen yaz&inodot;l&inodot;m ve uygulamalar&inodot;n&inodot;, BT envanterindeki sistemlerin zafiyet ve s&inodot;zma testlerinin yap&inodot;lmas&inodot;n&inodot; sa&gbreve;layacak,
 </li>
 <li>
 S&inodot;zma ve Zafiyet testleri sonras&inodot; belirlenen bulgular/uyumsuzluklar i&ccedil;in d&uuml;zeltici ve &ouml;nleyici faaliyetlerin al&inodot;nmas&inodot;ndan ve ilgili birimler ile takip edilmesinden sorumlu olacak,
 </li>
 <li>
 &Idot;&scedil; s&uuml;reklili&gbreve;i ve felaket kurtarma plan ve testlerinde s&uuml;re&ccedil; ve kalite ekibi ile koordine olacak.
 </li>
 </ul>
 
 
 
 
 
 Neden Ko&ccedil;Sistem ?
 
 
 <ul>
 <li>
 Akademi Plus-Teknik ve Ki&scedil;isel Geli&scedil;im E&gbreve;itimleri
 </li>
 <li>
 Ko&ccedil; Grubu ve &scedil;irket i&ccedil;i kariyer f&inodot;rsatlar&inodot;/rotasyon
 </li>
 <li>
 Tam kapsaml&inodot; &ouml;zel sa&gbreve;l&inodot;k sigortas&inodot;
 </li>
 <li>
 Online psikolog deste&gbreve;i
 </li>
 <li>
 Do&gbreve;um g&uuml;n&uuml; izni
 </li>
 <li>
 Kamp&uuml;ste spor merkezi ve Ko&ccedil; Toplulu&gbreve;u Spor Kul&uuml;b&uuml; f&inodot;rsatlar&inodot;
 </li>
 <li>
 Flextra - Esnek yan haklar paketi
 </li>
 <li>
 Sosyal Destek &Ouml;demeleri
 </li>
 <li>
 Mobil telefon ve internet
 </li>
 <li>
 TokenFlex dijital yemek kart&inodot;,
 </li>
 <li>
 Ko&ccedil; Ailem, Ko&ccedil; Akademi, Ko&ccedil; Healthcare e&scedil;li&gbreve;inde Ko&ccedil;lu olman&inodot;n ayr&inodot;cal&inodot;kl&inodot; d&uuml;nyas&inodot;.
 </li>
 </ul>
</div>

Bilgi Güvenliği Lideri

Gizli

<div>
 
 
 
 Objectives:
 
 
 
 
 
 
 
 The Information Security Officer is responsible for the oversight and ongoing improvement of the Cyber Security processes in the organization. Additionally, this role will be involved in the maintenance of standard operating procedures as they relate to the day-to-day operations of Security and Information Technology service delivery.
 
 
 The position is expected to implement global security rules in local country.
 
 
 
 
 
 
 
 Responsibilities:
 
 
 
 
 
 
 <ul>
 <li>
 Evaluate the country&rsquo;s security posture regularly
 </li>
 <li>
 Adjust the strategy to address emerging risks
 </li>
 <li>
 Ensure alignment with overall corporate objectives
 </li>
 <li>
 Identify and assess cybersecurity risks at country level
 </li>
 <li>
 Ensure that risks are addressed and integrated into the Group&rsquo;s Cyber Risk Mgmt. framework
 </li>
 <li>
 Take immediate action in the event of security incidents or breaches
 </li>
 <li>
 Coordinate with local business responsible &amp; CISO to mitigate risks and ensure timely communication
 </li>
 <li>
 Provide regular updates to the local Mgmt. Board, Global Cyber Security Management Lead &amp; CISO
 </li>
 <li>
 Inform on the progress of security initiatives, incidents, and deviations from security objectives
 </li>
 <li>
 Plan and implement awareness initiatives, incl. mandatory employee training &amp; specialized sessions for senior leadership
 </li>
 <li>
 Support local business to react much faster on security incidents and advise and suggest secure solution, assess &amp; improve security level in country
 </li>
 <li>
 Globally aligned cyber security strategy with highest standards to fulfill compliance needs
 </li>
 <li>
 Roll-out internal policies, standards, procedures and instructions
 </li>
 <li>
 Participate in internal and external audits
 </li>
 </ul>
 
 
 
 
 
 
 Necesarry Skills:
 
 
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in related fields
 </li>
 <li>
 Minimum of 4-5 years of experience in management of IT Security
 </li>
 <li>
 Advanced level of verbal and written English is a must
 </li>
 <li>
 Existing Security Certification (CISSP, CISM, CISA, etc.) or comparable will be plus
 </li>
 <li>
 Knowledge of ISO27001/2 will be plus
 </li>
 <li>
 Deep understanding of computer systems and networks
 </li>
 <li>
 Very good communication with stakeholders and persuasion skills
 </li>
 </ul>
 
 
</div>

Information Security Officer

Wyser

<div>
 
 Wyser is the international company within Gi Group Holding in charge of searching for and selecting specialized middle and senior management.
 
 
 We are looking for a "
 
 Chief Executive Officer"
 
 for our global business partner, which operates in financial services.
 
 
 
 
 
 
 About the Company
 
 
 
 
 
 
 The Chief Executive Officer will be responsible of all aspects in the organization, providing leadership in strategy, business growth, financial oversight, compliance, and regulatory affairs. This role requires guiding the company to remain competitive within the fast-moving, highly regulated financial services industry, while emphasizing innovation, customer experience, and operational excellence.
 
 
 
 
 
 
 
 
 
 About the Role
 
 
 
 
 
 
 This role blends the complexity of running a regulated financial institution with the fast pace of fintech innovation. The CEO will be expected to balance compliance, customer-focused innovation, and operational efficiency, ensuring the company remains profitable, future-ready, and a leader in digital financial services.
 
 This role will have no restriction for travelling in Southeast Europe.
 
 
 
 
 
 
 
 
 
 
 Responsibilities
 
 
 
 
 Strategic Leadership &amp; Vision
 
 
 <ul>
 <li>
 Define and implement the company&rsquo;s long-term strategy in line with industry trends, regulations, and customer expectations.
 </li>
 <li>
 Drive innovation and growth in the digital payments sector, identifying new business opportunities.
 </li>
 <li>
 Provide clear direction to the executive team and collaborate closely with the Board of Directors to achieve company objectives.
 </li>
 </ul>
 
 
 
 
 
 Financial Oversight &amp; Performance
 
 
 <ul>
 <li>
 Manage financial performance to achieve profitability targets, control expenses, and ensure stability.
 </li>
 <li>
 Responsible of budgeting, forecasting, and business planning.
 </li>
 <li>
 Cultivate relationships with investors, partners, and stakeholders to secure capital and support sustainable expansion.
 </li>
 </ul>
 
 
 
 
 
 Compliance &amp; Risk Management
 
 
 <ul>
 <li>
 Ensure full compliance with financial regulations, licensing obligations, AML/CTF standards, and data protection laws.
 </li>
 <li>
 Stay ahead of regulatory developments and adjust strategies accordingly.
 </li>
 <li>
 Establish strong risk management frameworks to protect against financial, operational, and reputational risks.
 </li>
 </ul>
 
 
 
 
 
 Innovation &amp; Product Development
 
 
 <ul>
 <li>
 Lead the creation of new digital financial products and services, driving customer adoption and market growth.
 </li>
 <li>
 Promote a culture of innovation by exploring advanced technologies such as AI, machine learning, and blockchain.
 </li>
 <li>
 Continuously enhance existing solutions to remain secure, user-friendly, and competitive.
 </li>
 </ul>
 
 
 
 
 
 Operational Excellence
 
 
 <ul>
 <li>
 Responsible daily operations to ensure efficiency, reliability, and superior customer service.
 </li>
 <li>
 Strengthen technological infrastructure to support secure and seamless digital transactions.
 </li>
 <li>
 Scale operations effectively to accommodate growing transaction volumes and user demands.
 </li>
 </ul>
 
 
 
 
 
 Customer Experience &amp; Relationship Management
 
 
 <ul>
 <li>
 Deliver best-in-class digital experiences across all platforms (web and mobile).
 </li>
 <li>
 Build and maintain strong relationships with key clients and partners to foster loyalty and revenue growth.
 </li>
 <li>
 Use customer insights to refine services and strengthen brand reputation.
 </li>
 </ul>
 
 
 
 
 
 Team Leadership &amp; Talent Development
 
 
 <ul>
 <li>
 Build and inspire a high-performing leadership team while nurturing a culture of accountability, innovation, and integrity.
 </li>
 <li>
 Mentor senior executives and develop emerging leaders across the organization.
 </li>
 <li>
 Encourage collaboration across departments to achieve business goals effectively.
 </li>
 </ul>
 
 
 
 
 
 External Representation
 
 
 <ul>
 <li>
 Act as the public face of the company at industry events, conferences, and media engagements.
 </li>
 <li>
 Maintain strong ties with regulators, financial institutions, fintech networks, and industry stakeholders.
 </li>
 <li>
 Communicate the company&rsquo;s mission, vision, and values to diverse audiences.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in business, Finance, Economics, or related field (MBA or master&rsquo;s preferred).
 </li>
 <li>
 At least 15 years in financial services or payments, including 10+ years in senior leadership (CEO, COO, CFO, CSO etc.).
 </li>
 <li>
 Proven experience leading an Electronic Money Institution or fintech company.
 </li>
 <li>
 Strong expertise in digital payments, PSD2 regulations, AML/CTF compliance, and fintech governance.
 </li>
 </ul>
 
 
 
 
 
 Required Skills
 
 
 <ul>
 <li>
 Exceptional leadership and communication abilities with a record of delivering results.
 </li>
 <li>
 In-depth knowledge of regulatory frameworks, EU directives, and fintech innovations.
 </li>
 <li>
 Strong financial management skills with large-scale P&amp;L responsibility.
 </li>
 <li>
 Experience scaling digital platforms and managing large customer bases.
 </li>
 </ul>
 
 
 
 
 
 Preferred Skills
 
 
 <ul>
 <li>
 Track record of successfully launching innovative financial products or services.
 </li>
 <li>
 Entrepreneurial mindset with excellent problem-solving capabilities.
 </li>
 <li>
 Familiarity with blockchain, digital assets, or emerging financial technologies.
 </li>
 <li>
 Passion for customer-focused design and technology-driven financial inclusion.
 </li>
 </ul>
 
 
 
 
 
 Pay range and compensation package
 
 
 <ul>
 <li>
 Competitive salary, performance-based bonuses, and stock options.
 </li>
 <li>
 Comprehensive benefits (healthcare, retirement, etc.).
 </li>
 <li>
 Opportunities for professional growth, including conferences and executive training.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Equal Opportunity Statement
 
 
 
 We are committed to diversity and inclusivity in our hiring practices.
 
 
 
 
 
 GI GROUP AND WYSER TURKEY SE&Ccedil;ME VE YERLE&Scedil;T&Idot;RME A.&Scedil;. T&uuml;rkiye &Idot;&scedil; Kurumu'nun 26.12.2023 tarihli 15198570 No'lu lisans sahibi &ouml;zel istihdam b&uuml;rosudur.
 
</div>

Chief Executive Officer

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 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>Assist the team and sites in responding to protocol-related or study-related or medical questions.
</li><li>Assist site staff with urgent and non-urgent safety events, and provide recommendations in accordance with the protocol.
</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: Hematology (Required)
</li><li><h2 class="jobSectionHeader">Applicants must have experience in at least one of the following areas: Hematology (Non-Malignant) , Hematological Malignancies , Pediatric Hematology / Adult Hematology
</h2></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 - Hematology , Home- Based

<div>
 
 
 Job Overview:
 
 
 
 As the Chief Compliance Officer, you will be fully responsible for establishing, implementing, monitoring, and maintaining the company's global compliance program. You will ensure all company activities strictly adhere to local financial regulations, Anti-Money Laundering (AML), and Counter-Financing of Terrorism (CFT) regulations in Turkey (our primary market) and other operating regions, with a specific focus on requirements for crypto assets. You will be the primary representative for all communications with regulatory bodies (such as BDDK, MASAK, CMB).
 
 
 
 
 
 
 Key Responsibilities:
 
 
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 Develop, review, and update the company's compliance policies, procedures, and control systems to address the rapidly changing regulatory landscape for cryptocurrencies in Turkey and internationally.
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 Act as the primary liaison for all communications, reporting, and responses to inquiries from regulatory agencies like the Financial Crimes Investigation Board (MASAK), Banking Regulation and Supervision Agency (BDDK), and Capital Markets Board (CMB).
 </li>
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 Ensure strict implementation of AML/CFT processes including Customer Due Diligence (KYC), Enhanced Due Diligence (EDD), transaction monitoring, and sanctions screening.
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 Oversee and ensure compliance with the Financial Action Task Force (FATF) "Travel Rule" and other international standards.
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 Lead the compliance team, providing compliance advisory, training, and guidance to all departments, fostering a strong culture of compliance.
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 Regularly report to the CEO and Board of Directors on the effectiveness of the compliance program, significant risk events, and regulatory developments.
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 Manage compliance-related audits and examinations and oversee the implementation of corrective actions.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
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 Bachelor's degree or higher in Law, Finance, Business, or a related field.
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 Minimum 3 years of compliance experience within Turkish financial institutions (banks, securities firms, payment institutions) or a renowned cryptocurrency exchange/custody platform,
 
 with a senior compliance management role.
 
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 <li>
 
 Deep understanding and practical experience with Turkish financial regulations, particularly Law No. 5549 on AML, MASAK regulations, and the latest regulations on crypto assets.
 
 International perspective is a plus.
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 Proven extensive experience interacting directly with Turkish financial regulatory agencies.
 </li>
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 Exceptional leadership, communication, and cross-functional collaboration skills.
 </li>
 <li>
 Fluency in English.
 </li>
 <li>
 Professional certifications such as CAMS, ICA are highly preferred.
 </li>
 </ul>
</div>

Chief Compliance Officer

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