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clinical trials assistant (single sponsor) turkey Jobs in Test Jobs In House Counsel Jobs In Istanbul

clinical trials assistant (single sponsor) turkey

experienced clinical research associate - sponsor dedicated - türkiye Jobs in Test Jobs In House Counsel Jobs In Istanbul

experienced clinical research associate - sponsor dedicated - türkiye

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hr manager - turkiye

klinik geliştirme asistanı - clinical development assistant (istanbul) Jobs in Test Jobs In House Counsel Jobs In Istanbul

klinik geliştirme asistanı - clinical development assistant (istanbul)

clinical trials assistant single sponsor turkey

IQVIA

<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>


<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>

<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, Turkey | Full time | Home-based | R1491925</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><br>
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA&rsquo;s suite of solutions to drive operational excellence and strategic leadership with our customers<br>
<br>
<b>Essential Functions</b></div><div><ul><li><br>
Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.</li><li>May be responsible for delivery and management of smaller, less complex, regional studies.</li><li>Develop integrated study management plans with the core project team.</li><li>Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.</li><li>Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.</li><li>Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.</li><li>Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.</li><li>Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.</li><li>Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.</li><li>May serve as primary or backup project contact with customer and would then own the relationship with the project&rsquo;s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;</li><li>Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;</li><li>Ensure the financial success of the project.</li><li>Forecast and identify opportunities to accelerate activities to bring revenue forward.</li><li>Identify changes in scope and manage change control process as necessary.</li><li>Identify lessons learned and implement best practices.</li><li>May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;</li><li>Adopt corporate initiatives and changes and serve as a change advocate when necessary.</li><li>Provide input to line managers of their project team members&rsquo; performance relative to project tasks.</li><li>Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;</li></ul><br>
<b>
Qualifications</b></div><div><ul><li><br>
Bachelor's Degree Life sciences or related field</li><li>5 years of prior relevant experience including &gt; 1 years project management experience or equivalent combination of education, training and experience.
</li><li>Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
</li></ul></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 Project Manager - IQVIA Biotech - Oncology

Henkel

<div>
 <strong>
  About this Position
 </strong>
 This role is responsible for leading key automotive OEM accounts in Turkey, aligning local execution with global strategies, and acting as the primary customer interface for commercial and technical topics. You will identify customer needs, drive new business opportunities, and support solution development in collaboration with Regional and Global KAMs. Additionally, you will execute account plans, manage CRM processes, and ensure sustainable growth in the Turkish automotive OEM market.
 <br/>
 <br/>
 <strong>
  What You&acute;ll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Leading automotive accounts in Turkey in line with Global OEM Strategies by Regional and Global KAMs
  </li>
  <li>
   Directly reporting to Automotive OEM Turkey Sales Manager
  </li>
  <li>
   Steering the OEM business with Global KAMs, Regional KAMs and to execute global and regional strategies in related OEMs locally
  </li>
  <li>
   Identifying needs of customers and finding accurate solution as a first point of contact with Global Technical teams,
  </li>
  <li>
   Regional and Global KAMs according to the necessity.
  </li>
  <li>
   Identifying business potentials in Turkey in related accounts and inform Technical Team and KAMs to develop a product according to needs of customer.
  </li>
  <li>
   Developing sales activities for the assigned customer portfolio across Turkey
  </li>
  <li>
   Preparing and implementing action plan to develop sales, increase the profit, and gain market share
  </li>
  <li>
   Executing customer roadmap and managing the closure respective CRM tool (ACE)
  </li>
  <li>
   Traveling around Turkey to participate in the trials of the customers in case of business necessities and analyzing market trends
  </li>
  <li>
   Performing forecasting and planning analysis for sustainability of stocks
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What makes you a good fit
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University degree in Engineering or related departments
  </li>
  <li>
   4 to 6 years of experience in technical sales
  </li>
  <li>
   SAP knowledge is a plus
  </li>
  <li>
   Strong communication and interpersonal skills with attitude in building relationships with professionals of all organizational levels
  </li>
  <li>
   Result oriented, self-motivating and team player
  </li>
  <li>
   Fluent in English both spoken and written
  </li>
  <li>
   Valid driving license and flexible for traveling
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Some perks of joining Henkel
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year
  </li>
  <li>
   Diverse national and international growth opportunities
  </li>
  <li>
   Global wellbeing standards with health and preventive care programs
  </li>
  <li>
   Gender-neutral parental leave for a minimum of 8 weeks
  </li>
  <li>
   Employee Share Plan with voluntary investment and Henkel matching shares
   <br/>
   <br/>
  </li>
 </ul>
 At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We look for a diverse team of individuals who possess different backgrounds, experiences, personalities and mindsets.
</div>


Associate Key Account Manager - Bus & Truck

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