purchasing specialist Jobs in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey

purchasing specialist

marketing specialist Jobs in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey

marketing specialist

customer service specialist Jobs in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey

customer service specialist

human resources specialist Jobs in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey

human resources specialist

planning specialist Jobs in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey

planning specialist

regulatory affairs specialist

Perrigo

<p></p><div><p>At Perrigo, we are driven by our mission to <b><i>Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All</i></b>. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing <b><i>The Best Self-Care for Everyone</i></b>, we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more. <b>We Are Perrigo</b>. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.</p><p></p><p><br>
Join us on our One Perrigo journey as we evolve to win in self-care.</p><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Description Overview</b></h2></div><div><p>
In this role you will be responsible for the hands on regulatory activities required to maintain existing commercial products, and support in making correct and timely new product applications of Perrigo products on the Turkish market. You will support to ensure compliance with the existing legislation for Medicines, Medical Devices, Biocides and Cosmetics. Another key aspect of the role will be supporting in the achievement of the overall Regulatory, Quality &amp; Safety objectives and timely realization of operational activities. In this position you collaborate closely with the Corporate Regulatory and Turkish Commercial colleagues to strive to help the customer the best.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Scope of the Role</b></h2></div><div><ul><li>
Support in the management of change by preparing applications and technical files in support of existing commercial product regulatory maintenance;</li><li>
Support in the regulatory activities on new product development (NPD), including artwork approvals, label claims and associated supporting documentation;</li><li>
Develop and approve label specifications (master text and local artwork text) in compliance with SOPs, as well as promotional materials from a regulatory perspective;</li><li>
Maintain regulatory files and data systems in compliance with SOPs;</li><li>
Represent regulatory affairs in project meetings with both Perrigo staff and external contacts;</li><li>
Follow up on changes in (inter)national regulations and legislations, and support in the interpretation, communication and implementation;</li><li>
Liaise with Corporate Regulatory, responding to regulatory queries and providing and review of registration documents as necessary for the Turkish and/or European territory;</li><li>
Support in the communication with local regulatory authorities regarding license applications and notice of change.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Experience Required</b></h2></div><div><ul><li>
University Degree in a Scientific Subject;</li><li>
Minimum of 2 years work experience within Regulatory Affairs required, within at least one of the following categories Medical Devices, Biocides, Cosmetics and Medicines;</li><li>
Excellent communicator in Turkish and English;</li><li>
Proficient computer skills esp. Microsoft (word, excel, powerpoint); experience with Veeva, TVT, Trackwise is an asset;</li><li>
Eye for detail, punctual, well organized;</li><li>
Being flexible and adaptable to change;</li><li>
Ability to support several concurrent projects/products simultaneously;</li></ul></div></div></div><p><b>
Benefits</b><br>
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.</p><p>
Find out more about <b>Total Rewards</b> at Perrigo.</p><p></p><p><b><br>
Hybrid Working Approach</b><br>
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.</p><p></p><p><br>
We are proud to be included in the Forbes list of &quot;America's Best Employers by State 2024&quot;. Find out more <b>here</b></p><p></p><p><b><br>
Applicants please note:</b> To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.</p><p></p><p><i><br>
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo</i></p></div>

Regulatory Affairs, Associate Specialist

ICON plc

<div>Site Specialist I, Study Start Up (Turkey, Ankara)<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Site Specialist I (Study Start Up Associate I) to join our diverse and dynamic team. As a Site Specialist I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.</div><div></div><div>
What you will be doing</div><ul><li><div>
Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.</div></li></ul><ul><li><div>
Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Maintaining accurate and up-to-date records of regulatory submissions and approvals.</div></li></ul><ul><li><div>
Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.</div></li></ul><ul><li><div>
Participating in study start-up meetings and providing input on regulatory requirements and timelines.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li><li><div>
Working knowledge of English and local language.</div></li></ul><ul><li><div>
Previous experience in clinical research or regulatory affairs preferred, but not required.</div></li></ul><ul><li><div>
Strong attention to detail and organizational skills.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><ul><li><div>
Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.</div></li></ul><div></div><div>
#LI-JJ1</div><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Site Specialist I, Study Start Up (Turkey, Ankara)

Calik Holding

<div>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor's degree in Law,
  </li>
  <li>
   3+ years of experience in compliance, legal, or regulatory roles,
  </li>
  <li>
   Strong understanding of national and international compliance standards,
  </li>
  <li>
   Excellent communication and analytical skills,
  </li>
  <li>
   Fluency in English; additional languages are plus.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Having interest and experience in regulatory and compliance matters,
  </li>
  <li>
   Possessing knowledge in analyzing and assessing compliance risks or sanctions,
  </li>
  <li>
   Conducting comprehensive work on the Compliance Program and preparing related procedures and policy documents,
  </li>
  <li>
   Providing training and awareness sessions to employees on ethics and compliance topics,
  </li>
  <li>
   Managing and monitoring the process of the Personal Data Protection Law, including handling VERBIS registrations and reporting,
  </li>
  <li>
   Working on ethical principles, ethics hotline, and compliance policy documents,
  </li>
  <li>
   Tracking legislative changes and informing companies accordingly,
  </li>
  <li>
   Supporting departments in preparing internal documents such as contracts, procedures, and policy texts,
  </li>
  <li>
   Responding to Due Diligence (DD) questionnaires and preparing company documentation.
  </li>
 </ul>
 <p>
 </p>
</div>


Compliance Lawyer

Yandex Go

<div>
 <p>
  Yandex is seeking an experienced
  <strong>
   Public Policy Lead
  </strong>
  to lead engagement with government authorities and key stakeholders across T&uuml;rkiye.
 </p>
 <p>
  <br/>
 </p>
 <p>
  As part of Yandex&rsquo;s International Public Policy team, you will help shape the regulatory environment for emerging mobility and digital platforms, represent Yandex&rsquo;s interests in key dialogues with public institutions, and support the company&rsquo;s growth strategy in T&uuml;rkiye.
 </p>
 <p>
  You&rsquo;ll work closely with business units such as Ride, Delivery, and Tech to align public policy priorities with business goals, anticipate regulatory challenges, and craft practical solutions that foster sustainable innovation in T&uuml;rkiye&rsquo;s mobility ecosystem.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What you&rsquo;ll do
  </strong>
 </p>
 <p>
  &bull; Develop and execute Yandex&rsquo;s public policy and government engagement strategy for T&uuml;rkiye
 </p>
 <p>
  &bull; Build and maintain strong relationships with ministries, regulators, municipalities, chambers, and other key stakeholders
 </p>
 <p>
  &bull; Monitor, analyze, and advise internal teams on legislative and regulatory developments that may affect Yandex&rsquo;s operations
 </p>
 <p>
  &bull; Prepare policy briefs, position papers, and consultation responses that reflect Yandex&rsquo;s views on mobility, digital platforms, and innovation
 </p>
 <p>
  &bull; Represent Yandex in meetings, forums, and industry associations, and contribute to public discussions on digital economy and platform regulation
 </p>
 <p>
  &bull; Support senior management and HQ executives during high-level government meetings, including the preparation of briefing materials and follow-up
 </p>
 <p>
  &bull; Manage external consultants, advisors, and associations supporting Yandex&rsquo;s advocacy efforts
 </p>
 <p>
  &bull; Coordinate cross-functional responses on public affairs matters with legal, compliance, operations, and communications teams
 </p>
 <p>
  &bull; Develop proactive initiatives that enhance Yandex&rsquo;s reputation as a responsible and innovative company
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What we&rsquo;re looking for
  </strong>
 </p>
 <p>
  &bull; Turkish citizenship with a deep understanding of T&uuml;rkiye&rsquo;s political and regulatory landscape
 </p>
 <p>
  &bull; 5+ years of experience in government relations, public policy, or regulatory affairs (ideally in technology, mobility, or telecom sectors)
 </p>
 <p>
  &bull; A strong network within central and local government institutions, particularly in ministries and agencies relevant to the digital economy and transportation
 </p>
 <p>
  &bull; Experience working with or within government agencies, parliament, or public sector consulting is an advantage
 </p>
 <p>
  &bull; An advanced degree in political science, law, public policy, economics, or a related field (preferred)
 </p>
 <p>
  &bull; Excellent communication and negotiation skills in Turkish and English
 </p>
 <p>
  &bull; Proven ability to analyze complex regulatory issues and turn them into actionable strategies
 </p>
 <p>
  &bull; Comfortable operating in a fast-paced, multicultural environment with multiple stakeholders
 </p>
 <p>
  &bull; Willingness to travel within T&uuml;rkiye and occasionally abroad
 </p>
</div>


Director of Government Affairs

KPMG Türkiye

<div>
 <p>
  KPMG is a global network of professional firms providing Audit, Tax and Advisory services. We operate in 146 countries and have more than 200.000 professionals working in member firms around the world. KPMG is one of the global leaders in Audit, Tax and Advisory services and the chosen business partner for many of the world&rsquo;s leading organizations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Quality and Risk Management (QRM) is a central team and is responsible for setting overall professional risk management and quality control policies and monitoring compliance, ethics and independence. This responsibility includes the need to understand and adhere to policies and associated procedures as well as local law requirements in carrying out their day-to-day activities. This team has an important role in identification, evaluation, management and monitoring of the most significant risks that the Firm faces and could threaten the achievement of its strategic objectives.
 </p>
 <p>
  Legal Affairs Junior Specialist will be an integral part of the QRM team reporting to the Legal Affairs Senior Manager.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor's degree in law and admission to the Turkish Bar Association,
  </li>
  <li>
   At least 1 year corporate experience is preferred,
  </li>
  <li>
   Knowledge and experience on standards and regulations issued by authorities (such as Public Oversight Accounting and Auditing Standards Authority, Capital Markets Board and Banking Regulation and Supervision Agency ) and in Data Protection Law,
  </li>
  <li>
   Strong understanding of Turkish Law and practice,
  </li>
  <li>
   Excellent command of English both in verbal and written,
  </li>
  <li>
   Good command of Microsoft Office programs,
  </li>
  <li>
   Proactive and self-motivated profile,
  </li>
  <li>
   Strong follow-up, timeliness,
  </li>
  <li>
   Good communication and teamwork skills.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Supports Legal Affairs Senior Manager and QRM Legal Team in QRM department in preparing, reviewing, negotiating and finalizing contracts with clients, suppliers or other third parties by taking both legislation and company procedures into consideration,
  </li>
  <li>
   Responds to the legal advice requests on daily business matters under the supervision of the Legal Affairs Senior Manager and QRM Legal Team,
  </li>
  <li>
   Continuously and closely follows up any changes in legislation and assist QRM team to ensure full compliance in business practices of KPMG,
  </li>
  <li>
   With respect to the escalated business and legal disputes, conflicts, litigations and queries; conducts the relevant practical and academic legal searches from relevant sources (such as precedent court decisions, legal books, legal opinions on specific competence areas) Supports in solving quality and risk related conflicts between KPMG and its clients or suppliers, drafts termination notifications,
  </li>
  <li>
   Contributing to the preparation and coordination of compliance reports at both global and local levels, ensuring alignment with internal policies and relevant legal regulations,
  </li>
  <li>
   Providing legal advice on various privacy and data protection issues, including compliance with KVKK, GDPR and data protection laws of other jurisdictions and following national and international legislation regarding the protection of personal data.
  </li>
 </ul>
</div>


Legal Affairs & Compliance Junior Specialist

Viatris

<div>Viatris &#304;la&ccedil;lar&#305; Ltd. &#350;ti<div></div><div>
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.<br>
<br>
Viatris empowers people worldwide to live healthier at every stage of life.<br>
<br>
We do so via:<br>
<br>
Access &ndash; Providing high quality trusted medicines regardless of geography or circumstance;<br>
Leadership &ndash; Advancing sustainable operations and innovative solutions to improve patient health; and<br>
Partnership &ndash; Leveraging our collective expertise to connect people to products and services.</div><div><br>
Every day, we rise to the challenge to make a difference, and here&rsquo;s how the Regulatory Relations Manager (Ankara) role will make an impact:</div><div></div><div>
The objective of this job is to be the single point of contact for Viatris Regulatory Affairs and Health Authority (HA) relations.</div><div></div><div>
Key responsibilities for this role include:</div><ul><li><div>
Interactions with Health Authority for regulatory submissions, approvals, follow-up submissions, quality compliance and all Istanbul manufacturing site related regulatory activities, out of stock communications, importation, sample analysis, GMP, face to face related discussions.</div></li><li><div>
Follows-up of all regulatory submissions/correspondences with Health Authority and notifies regulatory team in a timely manner.</div></li><li><div>
Follows-up sample analysis related to regulatory submissions.</div></li><li><div>
Reports pending regulatory approvals on a regular basis to ensure that all related Health Authority requests are attended.</div></li><li><div>
Ensures that all regulatory files are correctly maintained and secured as determined in procedures.</div></li><li><div>
Follows-up on local system updates, makes regulatory submission, queries and approval announcements and run regulatory systems reports.</div></li><li><div>
Residency in Ankara is required.</div></li></ul><div></div><div>
The minimum qualifications for this role are:</div><ul><li>
 University degree.</li><li>
 More than 5 years of experience in the same position.</li><li>
 Advanced Turkish and English in writing and speaking.</li><li>
 Male candidates must have completed their military service.</li><li>
 Ability to use Microsoft Office programs effectively.</li></ul><div></div><div>
At Viatris, we offer competitive salaries, benefits, and an inclusive environment where you can use your experiences, perspectives, and skills to help make an impact on the lives of others.</div><div></div><div>
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.</div><div></div><div>
Viatris is an Equal Opportunity Employer.</div></div><div></div>

Regulatory Relations Manager (Ankara)

Token Finansal Teknolojiler

<div>
 <p>
  <strong>
   Step into the future of fintech with us!
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  We&rsquo;re not just a company; we&rsquo;re a dynamic team of innovators pushing the boundaries of what&rsquo;s possible. We're on the lookout for passionate, forward-thinking Operations Specialist/Senior Specialist to join us on this exciting journey!
  <strong>
   Project Assistant &amp; Long Term Intern &ndash; Finance and Financial Affairs
  </strong>
  works cross-functionally to help businesses start using Token products as and quickly as possible.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   🔍Who We Are
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  At Token Financial Technologies, we lead Turkey&rsquo;s fintech revolution, empowering over 800,000 users and handling nearly 4 million transactions daily. Our flagship solutions, &Ouml;dero and TokenFlex, redefine payment systems and corporate benefits with cutting-edge technology. As part of Ko&ccedil; Holding and partnering with Beko, we&rsquo;re a team of innovators dedicated to driving progress and making a real impact in the financial world.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   ✨ What You&rsquo;ll Be Rocking
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Provide support in tracking and reporting daily financial transactions
  </li>
  <li>
   Contribute to data collection, verification, and comparison efforts during budget preparation processes
  </li>
  <li>
   Assist in updating and organizing financial statements
  </li>
  <li>
   Support expense, cost, and forecast analysis
  </li>
  <li>
   Create data sets using Excel and other reporting tools, and prepare content for presentations
  </li>
  <li>
   Ensure information flow with relevant internal and external stakeholders, compile and organize necessary documents
  </li>
  <li>
   Assist in process improvement and project efforts within the team
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   🎯 The Perfect Fit
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Preferably a graduate or senior student from the Faculty of Economics and Administrative Sciences (EAS)
  </li>
  <li>
   Proficient in English at a good level
  </li>
  <li>
   Recent graduate or 1-2 years of work experience
  </li>
  <li>
   Strong analytical skills, detail-oriented, and solution-focused
  </li>
  <li>
   Knowledge of financial analysis, accounting, or cost reporting processes is preferred (e.g., internships)
  </li>
  <li>
   Proficient in MS Excel, capable of supporting reporting and presentation preparation
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   🌐 Connect with us
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Web site: https://www.tokeninc.com/
 </p>
 <p>
  Linkedin:https://www.linkedin.com/company/tokeninc/
 </p>
 <p>
  Instagram: https://www.instagram.com/tokenfintech/
 </p>
 <p>
  YouTube:https://www.youtube.com/channel/UCaOpoQtYzio-s3KgGHuSPLA
 </p>
 <p>
 </p>
</div>


Project Assistant & Long Term Intern – Finance and Financial Affairs

Explore 340+ Regulatory affairs specialist in House Clinical Research Associate Site Management Jobs In House Clinical Research Associate Site Management Jobs In Turkey this November. Find roles across top companies and apply now to boost your career.