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(senior) clinical research associate - sponsor dedicated - türkiye Jobs in House Jobs In House Jobs In House Jobs In Istanbul

(senior) clinical research associate - sponsor dedicated - türkiye

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clinical trials assistant (single sponsor) turkey

senior clinical research associate sponsor dedicated t rkiye

IQVIA

<div>
 <strong>
  Senior Clinical Research Associate
  <br/>
  <br/>
 </strong>
 IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
 <br/>
 <br/>
 When you join
 <strong>
  IQVIA Turkey
 </strong>
 as a sponsor-dedicated CRA, you&rsquo;ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
 <br/>
 <br/>
 With access to world-class training and mentoring, you&rsquo;ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
 <br/>
 <br/>
 <strong>
  Your Responsibilities Will Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performing site selection, initiation, monitoring and close-out visits
  </li>
  <li>
   Supporting the development of a subject recruitment plan
  </li>
  <li>
   Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  </li>
  <li>
   Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  </li>
  <li>
   Collaborating with experts at study sites and with client representatives
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University degree in scientific discipline or health care
  </li>
  <li>
   At least 2 years of on-site monitoring experience
  </li>
  <li>
   Good knowledge of clinical research regulatory requirements
  </li>
  <li>
   Very good computer skills including MS Office
  </li>
  <li>
   Excellent command of Turkish and English language
  </li>
  <li>
   Organizational, time management and problem-solving skills
  </li>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers, and clients
  </li>
  <li>
   Flexibility to travel
  </li>
  <li>
   Driver&rsquo;s license class B
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Can Expect
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Resources that promote your career growth
  </li>
  <li>
   Leaders that support flexible work schedules
  </li>
  <li>
   Programs to help you build your therapeutic knowledge
  </li>
  <li>
   Better Work-Life balance, optimal DOS
  </li>
  <li>
   Excellent working environment in a stabile, international, reputable company
  </li>
  <li>
   Company car, mobile phone and attractive benefits package
   <br/>
   <br/>
  </li>
 </ul>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
</div>


(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Field-based | R1476111</div></div><p></p><div><div><div><div><b><br>
Senior Clinical Research Associate
</b></div><div>IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.</div><div>
When you join <b>IQVIA Turkey</b> as a sponsor-dedicated CRA, you&rsquo;ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
</div><div>With access to world-class training and mentoring, you&rsquo;ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.</div><div><b>
Your responsibilities will include:</b></div><ul><li>
Performing site selection, initiation, monitoring and close-out visits</li><li>
Supporting the development of a subject recruitment plan</li><li>
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution</li><li>
Collaborating with experts at study sites and with client representatives</li></ul><div><b><br>
Qualifications:</b></div><ul><li>
University degree in scientific discipline or health care</li><li>
At least 2 years of on-site monitoring experience</li><li>
Good knowledge of clinical research regulatory requirements</li><li>
Very good computer skills including MS Office</li><li>
Excellent command of Turkish and English language</li><li>
Organizational, time management and problem-solving skills</li><li>
Ability to establish and maintain effective working relationships with co-workers, managers, and clients</li><li>
Flexibility to travel</li><li>
Driver&rsquo;s license class B</li></ul><div><b>
What you can expect:
</b></div><ul><li>Resources that promote your career growth</li><li>
Leaders that support flexible work schedules</li><li>
Programs to help you build your therapeutic knowledge</li><li>
Better Work-Life balance, optimal DOS</li><li>
Excellent working environment in a stabile, international, reputable company</li><li>
Company car, mobile phone and attractive benefits package</li></ul></div></div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div></div></div><div></div>

<div>
 <strong>
  Clinical Research Associate
  <br/>
  <br/>
 </strong>
 <strong>
  IQVIA Turkey
 </strong>
 is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
 <br/>
 <br/>
 <strong>
  Your Responsibilities Will Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performing site selection, initiation, monitoring and close-out visits
  </li>
  <li>
   Supporting the development of a subject recruitment plan
  </li>
  <li>
   Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
  </li>
  <li>
   Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  </li>
  <li>
   Collaborating with experts at study sites and with client representatives
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University degree in scientific discipline or health care
  </li>
  <li>
   Requires at least 1 year of on-site monitoring experience.
  </li>
  <li>
   Experience in Pharma Industry, and/or Clinical Trials environment
  </li>
  <li>
   Very good computer skills including MS Office
  </li>
  <li>
   Excellent command of Turkish and English language, Turkey based
  </li>
  <li>
   Organizational, time management and problem-solving skills
  </li>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers, and clients
  </li>
  <li>
   Flexibility to travel
  </li>
  <li>
   Driver&rsquo;s license class B
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Can Expect
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Resources that promote your career growth
  </li>
  <li>
   Leaders that support flexible work schedules
  </li>
  <li>
   Programs to help you build your therapeutic knowledge
  </li>
  <li>
   Excellent working environment in a stabile, international, reputable company
  </li>
  <li>
   Company car, mobile phone and attractive benefits package
   <br/>
   <br/>
  </li>
 </ul>
 This role is suitable for disabled individuals. Priority will be given to candidates registered with &Idot;&Scedil;KUR.
 <br/>
 <br/>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
</div>


Experienced Clinical Research Associate - Sponsor dedicated - Türkiye

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Field-based | R1476113</div></div><p></p><div><div><b><br>
Clinical Research Associate</b></div><div><b>
IQVIA Turkey </b>is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.</div><div><b>
Your responsibilities will include:</b></div><ul><li>
Performing site selection, initiation, monitoring and close-out visits</li><li>
Supporting the development of a subject recruitment plan</li><li>
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines</li><li>
Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions</li><li>
Collaborating with experts at study sites and with client representatives</li></ul><div><b><br>
Qualifications:</b></div><ul><li>
University degree in scientific discipline or health care</li><li>
Requires at least 1 year of on-site monitoring experience.</li><li>
Experience in Pharma Industry, and/or Clinical Trials environment</li><li>
Very good computer skills including MS Office</li><li>
Excellent command of Turkish and English language, Turkey based</li><li>
Organizational, time management and problem-solving skills</li><li>
Ability to establish and maintain effective working relationships with co-workers, managers, and clients</li><li>
Flexibility to travel</li><li>
Driver&rsquo;s license class B</li></ul><div><b>
What you can expect:
</b></div><ul><li>Resources that promote your career growth</li><li>
Leaders that support flexible work schedules</li><li>
Programs to help you build your therapeutic knowledge</li><li>
Excellent working environment in a stabile, international, reputable company</li><li>
Company car, mobile phone and attractive benefits package</li></ul><div>
This role is suitable for disabled individuals. Priority will be given to candidates registered with İŞKUR.</div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div></div></div><div></div>

Eli Lilly

<div><p>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.</p><p></p><h3 class="jobSectionHeader"><b>
Overview</b></h3><p></p><p>
The Clinical Research Lead (CRL) is responsible for managing clinical investigators and sites participating in Lilly clinical trials and/or Post-Marketing Safety Studies. This includes investigator/site identification and qualification, ensuring timely trial enrollment aligned with scientific objectives, database lock delivery, issue resolution at trial sites, and maintaining inspection readiness at all times.</p><p>
The CRL ensures global program delivery through comprehensive investigator and site management, leveraging data and tools for informed decisions, and fostering high-quality interactions with clinical trial sites to provide an unparalleled customer experience. Additionally, the CRL oversees vendor monitoring activities, identifying and mitigating significant findings and trends.</p><p>
In countries without an Associate Director/Director of Investigator Engagement, the CRL may represent Investigator Engagement internally and externally, including interactions with regulatory bodies and influencing the local regulatory environment and strategy.</p><p></p><h3 class="jobSectionHeader"><b>
Primary Responsibilities</b></h3><p></p><p><b>
Clinical Investigator Management</b></p><ul><li>
Manage all activities at clinical trial sites, including site identification, qualification, enrollment planning, execution, and close-out.</li><li>
Ensure timely delivery of enrollment readiness, trial recruitment, and database locks through performance management and issue resolution.</li><li>
Identify opportunities to accelerate trial enrollment while maintaining an exceptional customer experience.</li><li>
Apply scientific, therapeutic area, and regional expertise to support trial execution and quality data delivery.</li><li>
Develop strategic institutional/site relationships to optimize clinical trial programs across therapeutic areas.</li></ul><p></p><p><b>
Clinical Trial Management</b></p><ul><li>
Implement investigator/site risk plans to meet enrollment and database lock commitments.</li><li>
Maintain site and country-level inspection readiness at all times.</li><li>
Use metrics to inform site/country/regional decision-making.</li><li>
Collaborate with internal and external teams to remove barriers to trial execution.</li><li>
Understand local treatment paradigms and standard of care to support feasibility and trial allocation.</li><li>
Provide vendor oversight for site monitoring activities.</li><li>
For countries with PMS requirements: manage Post-Marketing Safety Studies, including CRO selection, regulatory documentation, and project management.</li></ul><p></p><p><b>
Business Management and Engagement</b></p><ul><li>
Build strong professional relationships with clinical investigators to expand research partnerships and deliver an exceptional trial experience.</li><li>
Collaborate cross-functionally to align priorities and deliver the portfolio.</li><li>
Prospect targeted sites in line with portfolio strategy.</li><li>
Maintain therapeutic and technical expertise for scientific discussions with investigators and site staff.</li><li>
Act as a communication bridge between sites, vendors, and Lilly.</li><li>
Influence internal and external factors to improve clinical research delivery.</li></ul><p></p><p><b>
Country/Regulatory Responsibilities</b> <i>(where applicable)</i></p><ul><li>
Engage with regulatory bodies, ethical review boards, and national authorities to represent Lilly in the clinical trial environment.</li><li>
Participate in country pharmaceutical associations and affiliated bodies.</li><li>
Ensure compliance with local regulatory requirements and maintain internal processes accordingly.</li><li>
Contribute to external clinical development community initiatives and incorporate learnings into internal strategies.</li><li>
Support affiliate leadership in implementing regional initiatives.</li></ul><p></p><h3 class="jobSectionHeader"><b>
Minimum Qualifications</b></h3><ul><li>
Bachelor&rsquo;s degree or equivalent (preferably in a scientific or health-related field).</li><li>
Minimum 3 years of experience in pharmaceutical industry and/or clinical research.</li><li>
Strong knowledge of Good Clinical Practice (GCP).</li><li>
Ability to acquire and maintain therapeutic expertise to support portfolio needs.</li><li>
Excellent organizational and self-management skills.</li><li>
Strong communication skills (verbal and written) and ability to influence others.</li><li>
Strategic agility and broad business acumen.</li><li>
Demonstrated leadership behaviors and ability to lead in uncertain environments.</li></ul><p></p><h3 class="jobSectionHeader"><b>
Additional Preferences</b></h3><ul><li>
Strong organizational and planning skills.</li><li>
Ability to enhance customer experience.</li><li>
Fluent in English.</li><li>
Knowledge of country regulatory guidelines.</li><li>
Strong teamwork and interpersonal skills.</li><li>
Ability to develop innovative solutions.</li><li>
Travel required (50&ndash;75%).</li></ul><p></p><p>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.</p><p></p><p>
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.</p><p></p><p>
#WeAreLilly</p></div>

Clinical Research Lead

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Hybrid | R1497176</div></div><p></p><div><div><b><br>
Job Overview</b><br>
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.<br>
<br>
<b>Essential Functions</b></div><ul><li><div>
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.</div></li><li><div>
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.</div></li><li><div>
Assist with periodic review of study files for completeness.</div></li><li><div>
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.</div></li><li><div>
Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.</div></li><li><div>
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.</div></li><li><div>
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.</div></li></ul><div><b><br>
Qualifications</b></div><ul><li><div>
Bachelors Degree or equivalent</div></li><li><div>
Equivalent combination of education, training and experience.</div></li><li><div>
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.</div></li><li><div>
Written and verbal communication skills including good command of English language.</div></li><li><div>
Effective time management and organizational skills.</div></li><li><div>
Ability to establish and maintain effective working relationships with co-workers, managers, and clients.</div></li><li><div>
Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.</div></li><li><div>
Knowledge of applicable protocol requirements as provided in company training.</div></li></ul><div>
This role is suitable for disabled individuals. Priority will be given to candidates registered with İŞKUR.</div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div></div></div><div></div>

Clinical Trials Assistant (Single Sponsor) Turkey

<div>
 <strong>
  Job Overview
  <br/>
  <br/>
 </strong>
 Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
 <br/>
 <br/>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  </li>
  <li>
   Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  </li>
  <li>
   Assist with periodic review of study files for completeness.
  </li>
  <li>
   Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  </li>
  <li>
   Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  </li>
  <li>
   Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
  </li>
  <li>
   May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelors Degree or equivalent
  </li>
  <li>
   Equivalent combination of education, training and experience.
  </li>
  <li>
   Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
  </li>
  <li>
   Written and verbal communication skills including good command of English language.
  </li>
  <li>
   Effective time management and organizational skills.
  </li>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
  </li>
  <li>
   Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
  </li>
  <li>
   Knowledge of applicable protocol requirements as provided in company training.
   <br/>
   <br/>
  </li>
 </ul>
 This role is suitable for disabled individuals. Priority will be given to candidates registered with &Idot;&Scedil;KUR.
 <br/>
 <br/>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
</div>


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Clinical Research Lead

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Clinical Trials Assistant (Single Sponsor) Turkey