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site specialist ii, study start up Jobs in Ankara

site specialist ii, study start up

software technical product management senior specialist Jobs in Ankara

software technical product management senior specialist

senior study startup specialist

PSI CRO

<div><b>Company Description</b><p><br>
PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.</p><b><br>
Job Description</b><p><br>
Take your career to the next level and be involved in study startup processes in T&uuml;rkiye. You will provide direct operational support to project teams, ensure that clinical projects start smoothly and on time and support PSI in developing the local study startup team.</p><p>
Office-based in Ankara or remote</p><ul><li>
Perform study startup activities and support all processes critical for site activation.</li><li>
Collect site documents for IRB/IEC submission and/or IP-RED process.</li><li>
File study-specific documentation in TMF, in accordance with Document management plan.</li><li>
Compile IP-REDs packages assuring high quality.</li><li>
Review study-specific translations, including patient-facing documents.</li><li>
Support site agreement and/or budget negotiations, upon request.</li><li>
Ensure initial distribution of locally obtained clinical study supplies to sites and supervise initial distribution of Investigational Product(s) and centrally obtained clinical study supplies to sites.</li><li>
Identify project-specific issues and escalates to Regional (Startup) Lead/PM and operational Manager in the country.</li><li>
Develop site-specific startup timelines and is responsible for meeting the site activation targets under supervision.</li></ul><br>
<b>
Qualifications</b><br>
<ul><li>
College/University degree or an equivalent combination of education, training and experience</li><li>
At least 4 years' experience in clinical research</li><li>
At least 3 years of full-scope Study Startup experience in T&uuml;rkiye</li><li>
Excellent knowledge of ICH GCP, local laws and applicable regulations in the region</li><li>
Full working proficiency in English and Turkish</li><li>
Communication and organizational skills</li><li>
Ability to negotiate and build relationships at all levels</li></ul><br>
<b>
Additional Information</b><p><br>
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.</p></div>

Senior Study Startup Specialist

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 We are the company that cares &ndash; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.
 <br/>
 <br/>
 <strong>
  General Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
  </li>
  <li>
   Participate in the development and implementation of improvement strategies for the site identification process and related training activities
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Project Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Define the main study objectives and the optimal site profile
  </li>
  <li>
   Create initial list of potential sites
  </li>
  <li>
   Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
  </li>
  <li>
   In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
  </li>
  <li>
   Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
  </li>
  <li>
   In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
  </li>
  <li>
   Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University/college degree (Life Sciences/Pharmacy/Healthcare field is a plus), or an equivalent combination of education, training and experience
  </li>
  <li>
   Minimum 2 years of prior experience in site identification/study startup activities or equivalent
  </li>
  <li>
   Full professional working proficiency in Turkish and English
  </li>
  <li>
   Understanding of Good Clinical Practice, local laws and applicable regulations in Turkey
  </li>
  <li>
   Communication and collaboration skills
  </li>
  <li>
   Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.
</div>


Site Identification Specialist (Feasibility)

ICON plc

<div>Site Specialist II, Study Start Up<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 II (Study Start Up Associate II) to join our diverse and dynamic team. As a Site Specialist II at ICON, you will play a pivotal role in leading 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>
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.</div></li></ul><ul><li><div>
Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence</div></li></ul><ul><li><div>
Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.</div></li></ul><ul><li><div>
Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li></ul><ul><li><div>
Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.</div></li></ul><ul><li><div>
Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.</div></li></ul><ul><li><div>
Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><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 II, Study Start Up

<div>CRA II<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 Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies</div>
What you will be doing<ul><li>
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li></ul><ul><li>
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li></ul><ul><li>
Collaborating with investigators and site staff to facilitate smooth study conduct.</li></ul><ul><li>
Performing data review and resolution of queries to maintain high-quality clinical data.</li></ul><ul><li>
Contributing to the preparation and review of study documentation, including protocols and clinical study reports</li></ul>
Your profile<ul><li>
Bachelor's degree in a scientific or healthcare-related field.</li></ul><ul><li>
Minimum of 2 years of experience as a Clinical Research Associate.</li></ul><ul><li>
In-depth kNwledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li></ul><ul><li>
Strong organizational and communication skills, with attention to detail.</li></ul><ul><li>
Ability to work independently and collaboratively in a fast-paced environment.</li></ul><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>

CRA II

Trustlab

<div><p><b>About TrustLab</b></p><p>
TrustLab deploys custom LLMs as part of its AI solution for Enterprise customers. We&rsquo;re a fast-moving, venture-backed startup founded by senior leaders from Google, YouTube, TikTok, and Reddit, creating solutions for online safety, reputation and risk management. Our approach for human-in-the-loop AI solutions for content understanding is industry leading as a technology and business solution. We are looking for experienced and creative engineers to help us push the boundaries with emerging LLM technology applications, and leadership to deploy and scale our technology for customer use cases at scale.</p><p><b>
Job Title: Senior Full Stack Engineer (Python/React) &ndash; Ankara</b></p><h3 class="jobSectionHeader"><b>
About this role:</b></h3><p>
We&rsquo;re looking for a Senior Full Stack Engineer with a deep sense of ownership. This role is ideal for someone who thrives in fast-paced environments and wants to help define both the product and the technical direction of our platform. You'll work across the stack, focused both on building rich, performant, and intuitive interfaces that help users take action on complex, large-scale safety data, while designing the robust backend systems and APIs that power these experiences end-to-end.</p><p>
You&rsquo;ll join a small, mission-driven team where your contributions have a direct impact on real-world issues.</p><p><b>
Location:</b> Ankara, Turkiye<br>
<b>Experience:</b> 3+ years<br>
<b>Employment Type:</b> Full-time<br>
<br>
<b>What You&rsquo;ll Do:</b></p><ul><li><p>
Drive the development of end-to-end product features, working across both frontend and backend systems.</p></li><li><p>
Build clean, scalable backend services using Python (e.g., Django, FastAPI, or Flask).</p></li><li><p>
Develop rich, performant frontend applications using React, TypeScript, and modern tooling.</p></li><li><p>
Design and implement intuitive interfaces and workflows that empower analysts and reviewers working on online safety.</p></li><li><p>
Collaborate closely with product, design, data, and ML teams to ship impactful features quickly and iteratively.</p></li><li><p>
Own projects from start to finish, ensuring reliability, usability, and performance at every layer of the stack.</p></li><li><p>
Drive best practices in architecture, code quality, and testing across both frontend and backend systems.</p></li></ul><h3 class="jobSectionHeader"><b>
What We&rsquo;re Looking For:</b></h3><ul><li><p>
3+ years of professional software development experience.</p></li><li><p>
Strong experience in backend development in Python with frameworks like Django, FastAPI, or Flask.</p></li><li><p>
Strong experience building frontend applications with React and TypeScript.</p></li><li><p>
Strong UX sensibility and attention to detail in implementing clean, user-friendly interfaces.</p></li><li><p>
Comfort working independently in fast-changing or ambiguous environments.</p></li><li><p>
A collaborative mindset and passion for mission-driven work.</p></li><li><p>
Based in Ankara, Turkiye, some in-office time is required.</p></li></ul><h3 class="jobSectionHeader"><b>
Bonus Points:</b></h3><ul><li><p>
Experience in AWS</p></li></ul><h3 class="jobSectionHeader"><b>
Opportunities &amp; Perks:</b></h3><ul><li><p>
Work on cutting-edge AI technologies shaping the future of online safety.</p></li><li><p>
Collaborate with a multidisciplinary team tackling some of the most challenging problems in content moderation.</p></li><li><p>
Competitive compensation, comprehensive benefits, and opportunities for professional growth.</p></li><li><p>
Flexible hybrid work culture with opportunities for in-person collaboration in our Ankara office located in Maidan.</p></li></ul></div><p></p>

Senior Full Stack Engineer (Python/React) – Ankara

<div>Sr CRA<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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.</div><div></div><div>
What You Will Be Doing:</div><ul><li>
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li><li>
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li><li>
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li><li>
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li><li>
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li></ul><div>
Your Profile:</div><ul><li>
Advanced degree in a relevant field such as life sciences, nursing, or medicine.</li><li>
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li><li>
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.</li><li>
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li><li>
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li><li><div>
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver&rsquo;s license</div></li></ul><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>

Senior CRA

Gülermak Heavy Industries Construction Contracting Co inc

<div>
 <p>
  <strong>
   Role Purpose
  </strong>
 </p>
 <p>
  The Cybersecurity Specialist is responsible for leading and coordinating G&uuml;lermak&rsquo;s global IT security operations in close collaboration with cybersecurity vendors. This role ensures the development, implementation, and enforcement of corporate security policies and procedures across all environments.
 </p>
 <p>
  The position includes continuous monitoring and response to security incidents, execution of internal audits and penetration tests, and maintaining compliance with international standards and regulatory frameworks. The specialist will also be accountable for designing and maintaining secure configurations across IT networks, infrastructure, applications, and devices.
 </p>
 <p>
  In addition to technical responsibilities, the role involves driving company-wide security awareness initiatives and working cross-functionally with internal teams and external partners to strengthen G&uuml;lermak&rsquo;s overall security posture.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  &bull; Coordinate with cybersecurity vendors to ensure continuous protection
 </p>
 <p>
  &bull; Develop, update, and enforce corporate cybersecurity policies and procedures
 </p>
 <p>
  &bull; Monitor, analyze, and report on security incidents to senior management
 </p>
 <p>
  &bull; Plan and execute penetration tests and internal security audits
 </p>
 <p>
  &bull; Proactively monitor cyber threats and implement preventive measures
 </p>
 <p>
  &bull; Lead incident response and forensic investigations in case of breaches
 </p>
 <p>
  &bull; Conduct risk assessments and vulnerability management
 </p>
 <p>
  &bull; Develop mitigation plans and track remediation efforts
 </p>
 <p>
  &bull; Ensure compliance with KVKK, GDPR, HIPAA, NIST, ISO 27001 and similar frameworks
 </p>
 <p>
  &bull; Manage and optimize security solutions including Azure Security, M365 Security, firewalls, and endpoint protection
 </p>
 <p>
  &bull; Experience in configuration of IT network, infrastructure, applications, and devices in secure environments
 </p>
 <p>
  &bull; Maintain documentation for disaster recovery and business continuity
 </p>
 <p>
  &bull; Organize -plan &amp; execute- security awareness programs for employees and promote a culture of security across departments
 </p>
 <p>
  &bull; Stay up to date with emerging threats, vulnerabilities, and best practices
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Qualifications
  </strong>
 </p>
 <p>
  &bull; Bachelor&rsquo;s degree in Cybersecurity, Information Technology, Computer Science, or related field
 </p>
 <p>
  &bull; Minimum 4 years of experience in cybersecurity roles
 </p>
 <p>
  &bull; Strong knowledge of Microsoft, Linux, ERP systems, M365, Azure, and network security
 </p>
 <p>
  &bull; Hands-on experience with SIEM, IDS/IPS, firewall management, and endpoint protection
 </p>
 <p>
  &bull; Familiarity with regulatory frameworks (KVKK, GDPR, HIPAA, NIST, ISO 27001)
 </p>
 <p>
  &bull; Experience in threat detection, incident response, and vulnerability remediation
 </p>
 <p>
  &bull; Proficiency in Azure Security Center (Microsoft Defender for Cloud), Microsoft Defender, and related tools
 </p>
 <p>
  &bull; Preferred certifications: CIS, CISSP, CISM, CEH, CompTIA Security+, Microsoft Security certifications: SC900, SC-200,
 </p>
 <p>
  &bull; Strong communication and coordination skills
 </p>
 <p>
  &bull; Ability to translate technical risks into business language for non-technical stakeholders
 </p>
 <p>
  &bull; Proactive, analytical, and detail-oriented mindset
 </p>
 <p>
 </p>
</div>


Cyber Security Specialist

Explore 49+ Senior study startup specialist in Ankara this November. Find roles across top companies and apply now to boost your career.