site identification specialist (feasibility) Jobs in Ankara

site identification specialist (feasibility)

clinical site associate

field specialist - sand control systems Jobs in Ankara

field specialist - sand control systems

field specialist - wellbore intervention Jobs in Ankara

field specialist - wellbore intervention

it specialist

site identification specialist feasibility

PSI CRO

<div>
 <p>
  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/>
  <br/>
  <br/>
 </p>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <p>
  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/>
 </p>
 <p>
  <u>
   Based in Ankara, T&uuml;rkiye
   <br/>
   <br/>
  </u>
 </p>
 <p>
  <strong>
   General Responsibilities:
   <br/>
   <br/>
  </strong>
 </p>
 <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/>
  </li>
 </ul>
 <p>
  <strong>
   Project Responsibilities:
   <br/>
   <br/>
  </strong>
 </p>
 <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>
 <p>
  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.
  <br/>
  <br/>
 </p>
</div>


Site Identification Specialist (Feasibility)

<div><b>Company Description</b><p><br>
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.</p><b><br>
Job Description</b><p><br>
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.</p><p>
Based in Ankara, T&uuml;rkiye</p><p><b>
General Responsibilities:</b></p><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</li></ul><p><b>
Project Responsibilities:</b></p><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</li></ul><br>
<b>
Qualifications</b><br>
<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</li></ul><br>
<b>
Additional Information</b><p><br>
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.</p></div>

Sitero LLC

<div><p>Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.</p>
<p>
This role will involve regulatory work to get the country and sites approved through the Regulatory Authority (RA) and Ethics Committees (ECs), as well as site activities from feasibility through close out visits. The ability to perform both Reg and CRA duties is required.</p><p></p><p><b><br>
Job Title: Senior Clinical Research Associate (Contract)
</b></p><p><b>Location: Turkey (Remote)
</b></p><p><b>Function: Clinical Operations and Regulatory<br>
</b></p><p></p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES:</b></p>
<ul>
<li>Primary point of contact for site personnel during life cycle of clinical trial. This includes study start up support, site activation, trial conduct and closeout of a clinical trial.</li>
<li>Provides support to the Global Project Lead and CTM during project start up to ensure timely site selection and feasibility. Assists with collection of essential documents from the site. applications/Approvals required.</li>
<li>Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety.</li>
<li>Familiarity with regulations surrounding conduct of clinical trials in all countries pertinent to your contract</li>
<li>Knowledge and ability to perform throughout the duration of the study any RA submissions, Central EC submission, Local EC submission, and any other country specific submissions required</li>
<li>Conduct Site qualification, site initiation, routine site monitoring close out visits (remote and onsite), Central monitoring in compliance with study protocol and ICH-GCP.</li>
<li>Expert documentation of monitoring priorities/activities via site visit confirmation and follow up letters, monitoring visit reports, and any trial associated logs.</li>
<li>Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breeches that can impact data integrity.</li>
<li>Ability to present essential function of CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings.</li>
<li>Assists the Global Project Lead in identification of out-of-scope activities.</li>
<li>Basic understanding of assigned projects scope, milestones and budget and manages site level activities to ensure project deliverables are met.</li>
<li>Provides support to the CTM and Global project lead in negotiation of site budgets and contracts.</li></ul><br>
<p></p>
<p><b>
EDUCATION AND EXPERIENCE REQUIRED:</b></p>
<ul>
<li>5 years of experience independently monitoring clinical drug trials</li>
<li>Completed at least 2 clinical trial application submissions in the past 5 years in each country pertinent to your contract</li>
<li>Rare Disease; Hepatology and Gastrology experience required</li>
<li>Bachelors degree in a life science field required</li></ul><br>
<p></p>
<p><b>
COMPENSATION &amp; BENEFITS:</b></p>
<p>
Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits.</p><p></p><p><b><br>
EMPLOYMENT TYPE:</b></p>
<p>
Contract; 0.5-0.75 FTE availability required.</p><p></p><p><b><br>
COMMITMENTS:</b></p>
<ul>
<li>5-0.75 FTE availability</li>
<li>Willing to work in shifts as and when needed.</li>
<li>Ability to travel up to 80% for site monitoring and regulatory purposes</li>
<li>Ability to lift 1-50 pounds at varying times</li>
<li>Ability to stand for long durations, kneel, bend, and sit for varying periods of time</li></ul><br>
<p></p>
<p><b>
DISCLAIMER:</b></p>
<p>
Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.</p></div>

Senior Clinical Research Associate (Contract)

PharmEng Technology

<div>
 <strong>
  About The Job Quality Assurance Consultant
  <br/>
  <br/>
 </strong>
 <strong>
  Job Summary:
 </strong>
 The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   QMS implementation, maintenance, and oversight in local affiliates.
  </li>
  <li>
   Maintenance of the local Quality Manual and Site Master File.
  </li>
  <li>
   Quality risk management in local affiliate, including risk identification, analysis, communication, control, and escalation as required.
  </li>
  <li>
   Complaint management, acting as the Local Complaint Coordinator for reporting, local assessment, and local investigation.
  </li>
  <li>
   Change control management, QA assessment, site change control, QA review for change implementation and closure.
  </li>
  <li>
   Deviation management for internal, external, and transport deviations.
  </li>
  <li>
   CAPA management from deviations, internal audits, external audits, and self-inspections.
  </li>
  <li>
   Management of authority inspections and self-inspections.
  </li>
  <li>
   Local GxP surveillance and assessment.
  </li>
  <li>
   Product quality review (PQR).
  </li>
  <li>
   Training management, including maintenance of training matrix, training of local staff, annual GxP refresher training, and handling of training assignments in the LMS.
  </li>
  <li>
   Local product release (local QP), shipment review of transport performance, goods receipt check, and deviation handling.
  </li>
  <li>
   Oversight of GDP requirements for local warehousing and distribution.
  </li>
  <li>
   Shipping lane qualification and local transport performance of secondary distribution.
  </li>
  <li>
   Secondary distribution transport performance review.
  </li>
  <li>
   Return management, including QA evaluation against return criteria and collaboration with distributors.
  </li>
  <li>
   Product recall management, including local recall execution, communication with customers, communication with HA, recall reconciliation, and local product destruction.
  </li>
  <li>
   GxP suppliers management, including supplier identification, qualification, approval, annual compliance status evaluation, quality audit planning, conduct quality audits, and CAPA approval and closure.
  </li>
  <li>
   Local repackaging and relabeling, including change management, protocol, execution, QA review, and release.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Quality Management, Life Sciences, or a related field.
  </li>
  <li>
   Minimum of 5 years of experience in Quality Assurance within the pharmaceutical or healthcare industry.
  </li>
  <li>
   Strong knowledge of GxP regulations and quality standards.
  </li>
  <li>
   Excellent analytical, problem-solving, and communication skills.
  </li>
  <li>
   Ability to work independently and collaboratively in a team environment.
  </li>
  <li>
   Proficiency in using Quality Management Systems and Learning Management Systems (LMS).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Attention to detail and accuracy.
  </li>
  <li>
   Strong organizational and time management skills.
  </li>
  <li>
   Effective leadership and team management abilities.
  </li>
  <li>
   Proactive and results-oriented mindset.
  </li>
 </ul>
</div>


Quality Assurance Consultant

MAD Parfumeur

<div>
 <p>
  <strong>
   About Us
  </strong>
 </p>
 <p>
  Mad Parfumeur is one of the leading players in the Turkish perfume and cosmetics industry. We are seeking an experienced
  <strong>
   Production Development Specialist
  </strong>
  to join our production operations in
  <strong>
   Ankara
  </strong>
  and contribute to continuous improvement, process optimization, and manufacturing efficiency initiatives.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <strong>
   Process Improvement &amp; Efficiency Enhancement
  </strong>
 </p>
 <ul>
  <li>
   Analyze production bottlenecks and develop improvement projects
  </li>
  <li>
   Lead and implement Lean manufacturing techniques (Kaizen, 5S, SMED, etc.)
  </li>
  <li>
   Evaluate OEE, scrap rates, downtime, and cycle times to identify improvement areas
  </li>
  <li>
   Develop methods, standardizations, and workflow enhancements to increase production efficiency
  </li>
 </ul>
 <p>
  <strong>
   Product &amp; Process Development
  </strong>
 </p>
 <ul>
  <li>
   Evaluate the manufacturability of new products and collaborate with R&amp;D on process development
  </li>
  <li>
   Assess raw materials, formulas, and process steps for manufacturability and cost efficiency
  </li>
  <li>
   Conduct tests for formula/process modifications and prepare technical test reports
  </li>
 </ul>
 <p>
  <strong>
   Production Data Analysis &amp; Reporting
  </strong>
 </p>
 <ul>
  <li>
   Analyze production data and prepare capacity, efficiency, scrap, and performance reports
  </li>
  <li>
   Monitor daily/weekly/monthly KPI sets and present results to management
  </li>
  <li>
   Identify improvement opportunities through data-driven insights
  </li>
 </ul>
 <p>
  <strong>
   Equipment &amp; Line Optimization
  </strong>
 </p>
 <ul>
  <li>
   Develop improvement actions to enhance the technical performance of production lines
  </li>
  <li>
   Ensure standardization of machine settings and create relevant technical documentation
  </li>
  <li>
   Support feasibility studies for new equipment and technology investments
  </li>
 </ul>
 <p>
  <strong>
   Quality &amp; Standards Compliance
  </strong>
 </p>
 <ul>
  <li>
   Verify alignment of production processes with quality standards
  </li>
  <li>
   Perform root-cause analyses for product or process deviations
  </li>
  <li>
   Collaborate with Quality Assurance to manage corrective/preventive actions (CAPA)
  </li>
 </ul>
 <p>
  <strong>
   Cross-Functional Collaboration
  </strong>
 </p>
 <ul>
  <li>
   Work closely with R&amp;D, quality, production, planning, maintenance, and technical teams
  </li>
  <li>
   Ensure accurate transfer of formula changes, process updates, and technical requirements to production
  </li>
  <li>
   Provide technical guidance and training to production teams when needed
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in industrial, chemical, mechanical engineering or related technical fields
  </li>
  <li>
   Minimum 5 years of experience in production development, process improvement, or manufacturing engineering
  </li>
  <li>
   Strong knowledge of Lean manufacturing principles (Kaizen, 5S, OEE, SMED, etc.)
  </li>
  <li>
   Proficient in data analysis, MS Excel, and reporting tools
  </li>
  <li>
   Preferably experienced in cosmetics/chemical manufacturing or filling&ndash;mixing processes
  </li>
  <li>
   Strong analytical thinking, problem-solving, and technical evaluation skills
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Why Join Us?
  </strong>
 </p>
 <p>
  Working at Mad Parfumeur means being part of an innovative and fast-growing organization where you can make a real impact. You&rsquo;ll have the opportunity to grow professionally while contributing to a creative and high-paced production environment.
 </p>
</div>


Production Development Specialist

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>
 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.
 <br/>
 <br/>
 We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As a CSA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
 <br/>
 <br/>
 <strong>
  What You Will Be Doing
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assisting in the planning, initiation, and execution of clinical trial activities
  </li>
  <li>
   Conducting site feasibility assessments and participating in site selection processes
  </li>
  <li>
   Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
  </li>
  <li>
   Monitoring study progress and data collection activities to ensure quality and accuracy
  </li>
  <li>
   Assisting in the preparation and review of study documentation and reports
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your profile
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in a relevant field, such as life sciences or healthcare
  </li>
  <li>
   Previous experience in clinical research or a related field preferred
  </li>
  <li>
   Strong organizational and communication skills
  </li>
  <li>
   Ability to work independently and collaboratively in a fast-paced environment
  </li>
  <li>
   Attention to detail and ability to prioritize tasks effectively
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What ICON Can Offer You
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Our Benefits Examples Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Various annual leave entitlements
  </li>
  <li>
   A range of health insurance offerings to suit you and your family&rsquo;s needs.
  </li>
  <li>
   Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  </li>
  <li>
   Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family&rsquo;s well-being.
  </li>
  <li>
   Life assurance
  </li>
  <li>
   Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
   <br/>
   <br/>
  </li>
 </ul>
 Visit our careers site to read more about the benefits ICON offers.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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 or submit a request here
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 Are you a current ICON Employee? Please click here to apply
 <br/>
 <br/>
</div>


Clinical Site Associate

Explore 60+ Site identification specialist feasibility in Ankara this December. Find roles across top companies and apply now to boost your career.

60 site identification specialist feasibility jobs IN Ankara

Site Identification Specialist (Feasibility)

Site Identification Specialist (Feasibility)

Senior Clinical Research Associate (Contract)

Quality Assurance Consultant

Production Development Specialist

Site Specialist II, Study Start Up

Clinical Site Associate