license compliance investigator

Dassault Systèmes

<div><div><p>At Dassault Syst&egrave;mes, we help businesses and people imagine sustainable innovations that harmonize product, nature, and life. Protecting the integrity of our solutions and our ecosystem is essential to that mission.</p><p>
As a License Compliance Investigator, you will contribute to the execution of Dassault Syst&egrave;mes&rsquo; Anti-Piracy &amp; License Compliance Program across the EUROMED region. You will identify, investigate, and manage license compliance leads generated through internal and external sources, working in close collaboration with Sales, Partners, and Legal teams to convert compliance cases into business opportunities.</p><p>
In this role, you will also support actions aimed at detecting and deterring illegal use, distribution, or counterfeiting of Dassault Syst&egrave;mes solutions, in coordination with relevant external stakeholders where appropriate.</p><p>
If you are comfortable navigating complex situations, influencing stakeholders, and driving outcomes with a business-oriented and collaborative mindset, this role offers a unique opportunity to combine investigation, negotiation, and value creation.</p><h3 class="jobSectionHeader"><b>
Role &amp; Responsibilities</b></h3><ul><li>
Contribute to the development and continuous improvement of the Anti-Piracy &amp; License Compliance Program infrastructure</li><li>
Collaborate with global and regional Legal teams to manage compliance and legal engagement frameworks</li><li>
Coordinate and manage external investigation, audit, and legal service providers within the assigned region</li><li>
Act as a trusted partner for different channels, internal sales teams, and the partner ecosystem to support compliance objectives</li><li>
Identify, qualify, and investigate high-quality license compliance leads across multiple sales channels</li><li>
Manage compliance communications, including soft and standard notifications, follow-ups, and tailored correspondence</li><li>
Ensure accurate, consistent, and timely data management across multiple internal systems and tools</li><li>
Support the creation, qualification, and ownership of sales opportunities resulting from compliance activities</li><li>
Investigate cases involving unauthorized use, illegal distribution, or counterfeiting of Dassault Syst&egrave;mes solutions</li><li><p>
Engage, when required, with external authorities and industry bodies to support enforcement and compliance actions</p></li></ul></div><p></p><div><h3 class="jobSectionHeader"><b><br>
Qualifications</b></h3><ul><li>
Bachelor&rsquo;s or Master&rsquo;s degree in Business or related field</li><li>
Experience in a role requiring a strong focus on analytical activities, investigation, or data-driven decision making</li><li>
Strong written and verbal communication skills in a professional business environment</li><li>
Proven ability to influence stakeholders and demonstrate leadership by bringing together contributors from diverse disciplines</li><li>
Strong negotiation skills, with the ability to manage discussions and drive consensus among multiple parties</li><li>
Demonstrated ability to manage conflict and bring sensitive situations to a constructive and successful conclusion</li><li><p>
Highly enthusiastic, committed, and motivated, with a strong sense of ownership and accountability</p></li><br>
<p></p><li>
Strong prioritization skills, with the ability to remain focused despite competing inputs and stakeholder influence</li><li>
Comfortable working with multiple tools, systems, and technologies</li><li>
Knowledge of software licensing models and contractual principles is a strong plus</li><li>
Excellent business communication skills in Turkish and English</li></ul><h3 class="jobSectionHeader"><b>
What&rsquo;s in it for you</b></h3><ul><li>
An international and diverse working environment within a collaborative, inclusive team</li><li>
Flexible working hours with a hybrid working model, supporting a healthy work&ndash;life balance</li><li>
Extensive learning, skills development, and career growth programs to support your long-term journey with us</li><li>
A comprehensive benefits package, including private health insurance and meal vouchers</li></ul></div><h2 class="jobSectionHeader"><b>
Inclusion statement</b></h2><div>
As a game-changer in sustainable technology and innovation, Dassault Syst&egrave;mes is striving to build more inclusive and diverse teams across the globe. We believe that our people are our number one asset and we want all employees to feel empowered to bring their whole selves to work every day. It is our goal that our people feel a sense of pride and a passion for belonging. As a company leading change, it&rsquo;s our responsibility to foster opportunities for all people to participate in a harmonized Workforce of the Future.</div></div>

License Compliance Investigator

Parexel

<div>
 <strong>
  Key Accountabilities
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 <strong>
  Site Management Responsibilities
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 </strong>
 <ul>
  <li>
   Contributes to the selection of potential investigators.
  </li>
  <li>
   In some countries, as required, Sr CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
  </li>
  <li>
   Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
  </li>
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   Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are always inspection ready.
  </li>
  <li>
   Actively participates in Local Study Team (LST) meetings.
  </li>
  <li>
   Contributes to National Investigators meetings, as applicable.
  </li>
  <li>
   Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
  </li>
  <li>
   Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
  </li>
  <li>
   Updates CTMS and other systems with data from study sites as per required timelines.
  </li>
  <li>
   Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
  </li>
  <li>
   Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits.
  </li>
  <li>
   Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
  </li>
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   Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
  </li>
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   Ensures data query resolution in a timely manner.
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   Works with data management to ensure robust quality of the collected study data.
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   Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
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   Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
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   Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
  </li>
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   Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
  </li>
  <li>
   Assists site in maintaining inspection ready ISF.
  </li>
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   Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
  </li>
  <li>
   Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICHGCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
  </li>
  <li>
   Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
  </li>
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   Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
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   Collaborates with local Medical Scientific Liaisons (MSLs) as directed by LSAD or line manager
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  </li>
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  Compliance with Sponsor Standards
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   Ensures compliance with the Client&rsquo;s Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).
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   Ensures compliance with local, national, and regional legislation, as applicable.
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   Completes timesheets accurately as required
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  </li>
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  Compliance with Parexel Standards
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 <ul>
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   Complies with required training curriculum.
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   Completes timesheets accurately as required.
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   Submits expense reports as required.
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   Updates CV as required.
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   Maintains working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements.
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  Skills (Essential)
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   Excellent attention to detail.
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   Good written and verbal communication skills.
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   Good collaboration and interpersonal skills.
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   Good negotiation skills.
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   Proficient in written and spoken English language required.
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  <li>
   Fluency in local language(s) required.
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  </li>
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  Skills (Desirable)
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   Ability to work in an environment of remote collaborators. Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
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   Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
  </li>
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   Good analytical and problem-solving skills.
  </li>
  <li>
   Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  </li>
  <li>
   Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
  </li>
  <li>
   Team oriented and flexible; ability to respond quickly to shifting demands and opportunities Knowledge and Experience (Essential):
  </li>
  <li>
   Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
  </li>
  <li>
   Good knowledge of relevant local regulations.
  </li>
  <li>
   Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
  </li>
  <li>
   Basic understanding of the drug development process.
  </li>
  <li>
   Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
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  </li>
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  Knowledge And Experience (Desirable)
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  <li>
   Familiar with risk-based monitoring approach including remote monitoring.
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   Good cultural awareness.
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  Education
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 <ul>
  <li>
   Bachelor&rsquo;s degree in related discipline, preferably in life science, (or equivalent adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
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  </li>
 </ul>
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  Other
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  <li>
   Ability to travel nationally/internationally as required.
  </li>
  <li>
   Valid driving license per country requirements, as applicable
  </li>
 </ul>
</div>


Senior Clinical Research Associate & CRAII  - FSP (Open)

<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

袁记云饺 YUEN KEE DUMPLING

<p>Job Responsibilities</p><ul><li>Implement strategies and policies established by the Board of Directors.</li><li>Manage day-to-day operations, including HR, marketing, finance, and production.</li><li>Organize the company&rsquo;s internal structure and business functions.</li><li>Recruit and manage employees.</li><li>Report regularly to the Board of Directors.</li><li>Sign contracts and commitments within the scope of authorization.</li><li>Ensure compliance and support audits and inspections.</li></ul><p>Job Requirements</p><ul><li>Must hold a four-year bachelor&rsquo;s degree and have at least 7 years of work experience in the financial or technology sector.</li><li>Must work full-time in T&uuml;rkiye.</li><li>Appointment must be approved by the Board of Directors.</li><li>Must not be bankrupt or undergoing financial restructuring.</li><li>Must not hold more than 10% equity in any financial institution.</li><li>Must have no serious criminal convictions (such as fraud, bribery, terrorism, etc.).</li><li>Must not be legally prohibited from engaging in trading activities.</li><li>Must not be responsible for incidents that resulted in license revocation.</li><li>Must have no administrative penalties in the past five years.</li></ul><p>Job Type: Full-time</p><p>Pay: 400,000.00TRY per month</p><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li> financial or technology sector.: 7 years (Required)</li></ul><p>Location:</p><ul><li>ıstanbul (Preferred)</li></ul>

General Manager

Gizli

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  <strong>
   Responsibilities
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 </p>
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 </p>
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  <li>
   Represent the company before judicial, administrative, and other official authorities,
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   Conduct the litigation and mediation processes in which the company is a party,
  </li>
  <li>
   Initiate and finalize enforcement proceedings regarding receivables,
  </li>
  <li>
   Prepare, review, and negotiate dealership, procurement, and service agreements,
  </li>
  <li>
   Provide legal consultancy to internal departments,
  </li>
  <li>
   Ensure coordination with external attorneys regarding outsourced legal services and manage report procurement processes,
  </li>
  <li>
   Follow compliance processes related to Competition Law and Personal Data Protection Law (KVKK), and ensure communication and coordination with the consulting firm,
  </li>
  <li>
   Prepare Board of Directors and General Assembly resolutions, conduct and coordinate trade registry procedures.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Graduated from the Faculty of Law and registered with the Bar Association,
  </li>
  <li>
   1&ndash;3 years of practical experience at a Law Firm or as an in-house lawyer (preferably with experience in the automotive sector),
  </li>
  <li>
   Experience in Consumer Law, Enforcement Law, Corporate Law, and Labor Law,
  </li>
  <li>
   Experience in court hearings,
  </li>
  <li>
   Proficient in using UYAP applications,
  </li>
  <li>
   Sufficient English proficiency to effectively participate in meetings conducted in English,
  </li>
  <li>
   Class B driver&rsquo;s license, and with no travel restrictions,
  </li>
  <li>
   Proficient in using MS Office programs,
  </li>
  <li>
   Strong planning and organizational skills,
  </li>
  <li>
   Team-oriented with strong representation skills.
  </li>
 </ul>
 <p>
 </p>
</div>


Lawyer

Mercedes-Benz Otomotiv

<div>
 <p>
  Are you passionate about the automotive industry and skilled in building strong business relationships? Join us as a Fleet and Special Sales Coordinator and play a key role in driving Mercedes-Benz passenger car sales to public sector customers, diplomatic clients, and major corporate accounts.
 </p>
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  <strong>
   What You&rsquo;ll Do:
  </strong>
 </p>
 <ul>
  <li>
   Coordinate fleet and special sales for public institutions, diplomatic clients, and corporate key account companies.
  </li>
  <li>
   Manage discount approvals and ensure accurate documentation and compliance.
  </li>
  <li>
   Build and maintain strong relationships with key accounts through regular visits and proactive engagement.
  </li>
  <li>
   Collaborate with internal teams and dealer networks for seamless operations.
  </li>
  <li>
   Prepare reports and insights for management and liaise with Mercedes-Benz headquarters in Germany.
  </li>
  <li>
   Ensure data accuracy and integrity across all fleet-related systems.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What We&rsquo;re Looking For:
  </strong>
 </p>
 <ul>
  <li>
   Strong interpersonal and negotiation skills.
  </li>
  <li>
   Passion for passenger cars and solid knowledge of the automotive industry.
  </li>
  <li>
   Experience in sales or marketing (preferably automotive).
  </li>
  <li>
   Excellent communication in Turkish and English.
  </li>
  <li>
   Proactive, adaptable, and results-driven mindset.
  </li>
  <li>
   Bachelor&rsquo;s degree and valid driver&rsquo;s license.
  </li>
  <li>
   Advanced MS Office skills and willingness to travel frequently.
  </li>
 </ul>
 <p>
  <br/>
 </p>
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 </p>
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 </p>
 <p>
  <strong>
   Why Mercedes-Benz?
  </strong>
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  Be part of a global brand that sets the standard for innovation, quality, and customer experience.
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  <strong>
   Apply now and accelerate your career with Mercedes-Benz!
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 </p>
</div>


Fleet and Special Sales Coordinator

BSH Ev Aletleri Türkiye

<div>
 <p>
  Tomorrow is our home.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Find out how easily you can achieve this at BSH Home Appliances Group: As a leading manufacturer of home appliances and solutions, we encourage commitment and open-mindedness among our employees. With our global brands Bosch, Siemens, Gaggenau, and Neff as well as our local brands, our focus truly is on innovation. And that doesn&rsquo;t just apply to our products and services but also drives the way in which we cooperate, exchange ideas, and organize our teams. Everyone is invited to make their individual contribution to our overall success. Join us now and give your career a home.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Your Responsibilities
  </strong>
 </p>
 <p>
  / Lead and coordinate nationwide field merchandising operations, ensuring brand visibility and compliance with global retail guidelines.
 </p>
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  / Supervise and develop the merchandiser team, monitoring store execution quality, POSM usage, and campaign implementation.
 </p>
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  / Plan, track, and report in-store marketing activities, providing insights for continuous improvement.
 </p>
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  / Collaborate with Sales, Marketing, Product, and Retail Design teams to translate strategies into effective in-store actions.
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  / Manage third-party agencies and suppliers to ensure operational excellence, cost control, and timely execution.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Your Profile
  </strong>
 </p>
 <p>
  / Bachelor&rsquo;s degree in Marketing, Business Administration, Engineering, or related field.
 </p>
 <p>
  / Minimum 5 years&rsquo; experience in retail marketing, merchandising, or trade marketing.
 </p>
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  / Strong understanding of in-store marketing dynamics and field team management.
 </p>
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  / Excellent communication, organization, and problem-solving skills; fluent in English.
 </p>
 <p>
  / Willingness to travel frequently across Turkey; driving license preferred.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Your Benefits
  </strong>
 </p>
 <p>
  / Flexible working hours schemes and diverse career opportunities
 </p>
 <p>
  / Individual development programs and international perspectives
 </p>
 <p>
  / Modern healthcare services
 </p>
 <p>
 </p>
</div>


Retail Marketing Executive

Explore 290+ License compliance investigator in Istanbul Turkey this January. Find roles across top companies and apply now to boost your career.