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assistant procurement manager - turkiye & middle east

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ey türkiye - business transformation / consultant - senior consultant

hr manager - turkiye

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 | 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>

Experienced Clinical Research Associate - Sponsor dedicated - Türkiye

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

Medtronic

<div><p>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
</p><p></p><h1 class="jobSectionHeader"><b>A Day in the Life
</b></h1>Atrial fibrillation affects over 33 million individuals worldwide and is the most common form of serious arrhythmia. Being in a fast-growing cardiac ablation business segment and with recent acquisition of the AFFERA&trade; Mapping and Ablation System, we are poised to provide innovative solutions to address unmet needs for many patients. We are seeking a talented and motivated Senior AFFERA&trade; Therapy Account Consultant to join our team to further drive the growth of the business.
<br>
Reporting the operating unit this role is critical in providing expert clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA&trade; Mapping and Ablation System.
<p><b>Responsibilities may include the following and other duties may be assigned:
</b></p><ul><li>Provide proficient clinical and technical assistance to physicians and EP Lab Staff on the use of the Affera&trade;️ Mapping and Ablation System and related equipment (Generators, SW functionalities, pump and accessories).
</li><li>Serve as technical adviser/expert, demonstrating products/service, providing T&amp;E, in-service or trade show support and troubleshooting product issues.
</li><li>Adapt and contribute to short and long-range plans, goals, and objectives for the Affera&trade; Mapping and Ablation System. Adapt and deploy product / service value proposition.
</li><li>Conduct competitive product analysis, opportunity assessment and market research.
</li><li>Be an active participant to the development of advanced clinical workflows.
</li><li>Work closely with the education team and support the development of training centers.
</li><li>Stay abreast of all products information across the Medtronic CAS portfolio, instructions for use (IFU) and relevant scientific clinical literature and new product information.
</li><li>Be responsible for product launch strategies for new site activation as well as ensuring effective product placement relative to customer needs.
</li></ul><p></p><p><b>Required Knowledge and Experience:
</b></p><ul><li>Bachelor's degree required in electrical or medical engineering or related scientific disciplines or equivalent experience.
</li><li>3+ years of clinical EP experience.
</li><li>Minimum of 2 years of successful independent support of EP mapping procedures.
</li><li>IBHRE or equivalent certification is a plus.
</li><li>Fluency in English, any other European languages are advantageous.
</li><li>Valid driving license
</li><li>Ability to manage high-stress situations with a clear problem-solving mindset.
</li><li>Ability to ensure knowledge transfer to other colleagues and peers when requested.
</li><li>Ability to maintain a high level of responsiveness to customer or other internal and external stakeholders.
</li></ul><p></p><p><b>Physical Job Requirements
</b><br>
<br>
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
</p><p></p><h1 class="jobSectionHeader"><b>Benefits &amp; Compensation
</b></h1><p><b>Medtronic offers a competitive Salary and flexible Benefits Package
</b><br>
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.<br>
<br>
</p><p></p><h1 class="jobSectionHeader"><b>About Medtronic
</b></h1><p>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
<br>
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
<br>
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</p></div><p></p>

Senior Affera Mapper

Parexel

<div><p><b>Key Accountabilities:</b></p><p></p><div><div><div><div><div><div><div><div><div><p><b>
Site Management Responsibilities</b></p><ul><li><p>
Contributes to the selection of potential investigators.
</p></li><li><p>In some countries, as required, Sr CRAs are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
</p></li><li><p>Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
</p></li><li><p>Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are always inspection ready.
</p></li><li><p>Actively participates in Local Study Team (LST) meetings.
</p></li><li><p>Contributes to National Investigators meetings, as applicable.</p></li><li><p>
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
</p></li><li><p>Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate.
</p></li><li><p>Updates CTMS and other systems with data from study sites as per required timelines.
</p></li><li><p>Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.</p></li><li><p>
Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits.
</p></li><li><p>Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
</p></li><li><p>Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
</p></li><li><p>Ensures data query resolution in a timely manner.
</p></li><li><p>Works with data management to ensure robust quality of the collected study data.
</p></li><li><p>Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.</p></li><li><p>
Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with Client SOP.
</p></li><li><p>Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
</p></li><li><p>Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
</p></li><li><p>Assists site in maintaining inspection ready ISF.
</p></li><li><p>Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
</p></li><li><p>Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICHGCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
 </p></li><li><p>Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
</p></li><li><p>Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
</p></li><li><p>Collaborates with local Medical Scientific Liaisons (MSLs) as directed by LSAD or line manager</p></li></ul><p></p><p><b>
Compliance with Sponsor Standards</b></p><ul><li><p>
Ensures compliance with the Client&rsquo;s Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).</p></li><li><p>
Ensures compliance with local, national, and regional legislation, as applicable.
</p></li><li><p>Completes timesheets accurately as required</p></li></ul><p></p><p><b>
Compliance with Parexel Standards</b></p><ul><li><p>
Complies with required training curriculum.
</p></li><li><p>Completes timesheets accurately as required.
</p></li><li><p>Submits expense reports as required.
</p></li><li><p>Updates CV as required.
</p></li><li><p>Maintains working knowledge of and complies with Parexel/Client processes, ICH-GCPs and other applicable requirements.</p></li></ul><p><b>
Skills (Essential):</b>
</p><ul><li><p>Excellent attention to detail.
</p></li><li><p>Good written and verbal communication skills.
</p></li><li><p>Good collaboration and interpersonal skills.
</p></li><li><p>Good negotiation skills.
</p></li><li><p>Proficient in written and spoken English language required.
</p></li><li><p>Fluency in local language(s) required.
</p></li></ul><p><b>Skills (Desirable):</b>
</p><ul><li><p>Ability to work in an environment of remote collaborators. Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
</p></li><li><p>Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
</p></li><li><p>Good analytical and problem-solving skills.
</p></li><li><p>Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
</p></li><li><p>Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
</p></li><li><p>Team oriented and flexible; ability to respond quickly to shifting demands and opportunities Knowledge and Experience (Essential):
</p></li><li><p>Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. &bull; Good knowledge of relevant local regulations.
</p></li><li><p>Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
</p></li><li><p>Basic understanding of the drug development process.
</p></li><li><p>Good understanding of Clinical Study Management including monitoring, study drug handling and data management.</p></li></ul><p></p><p><b>
Knowledge and Experience (Desirable):</b>
</p><ul><li><p>Familiar with risk-based monitoring approach including remote monitoring.
</p></li><li><p>Good cultural awareness.
</p></li></ul><p></p><p><b>Education:</b>
</p><ul><li><p>Bachelor&rsquo;s degree in related discipline, preferably in life science, (or equivalent adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.</p></li></ul><p><b>
Other:</b></p><ul><li><p>
Ability to travel nationally/internationally as required.
</p></li><li><p>Valid driving license per country requirements, as applicable</p></li></ul></div></div></div></div></div></div></div></div></div></div>

Senior Clinical Research Associate & CRAII - FSP (Open)

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Home-based | R1502095</div></div><p></p><div><h3 class="jobSectionHeader"><b><i><br>
Drive innovation in clinical trial delivery with IQVIA &ndash; where your leadership empowers sites and accelerates patient recruitment.</i></b></h3><div><b>
About the Role</b></div><div><br>
IQVIA&rsquo;s Site Enablement Solutions (SES) provide trained, dedicated clinical research personnel to trial sites globally, reducing site burden and improving patient recruitment and data quality. As a Hybrid Site Enablement Lead &amp; Site-Facing Line Manager, you will enable and manage study-specific deliverables at clinical trial sites, supporting site-based staff and collaborating with internal teams to optimize performance across the study lifecycle. This is a home-based, fully remote role and does not include a company car.</div><div><b>
Key Responsibilities</b></div><ul><li>
Lead implementation of SES services at assigned sites, ensuring timely activation and adoption.</li><li>
Train site staff on SES tools and services, including Referral Hub and Direct-to-Patient (DTP) campaign workflows.</li><li>
Monitor referral funnel performance and follow up to optimize patient recruitment outcomes.</li><li>
Collaborate with legal and contracting teams to execute service agreements with sites.</li><li>
Interview, hire, and manage temporary site staff, including onboarding and performance oversight.</li><li>
Forecast effort and manage invoicing for assigned sites.</li><li>
Maintain strong site relationships and ensure continuous feedback loops.</li><li>
Track and report on service delivery impact and quality metrics.</li><li>
Support process improvement initiatives and contribute to SES operational excellence.</li><li>
Ensure administrative compliance including timecoding, timesheet completion, and supply logistics.</li><li>
Conduct regular one-on-ones and performance reviews with site workers.</li><li>
Serve as escalation point for site worker challenges and operational issues.</li></ul><div><b>
Qualifications</b></div><ul><li>
Bachelor&rsquo;s degree or higher in health sciences or related field.</li><li>
3&ndash;5 years of clinical research experience, preferably in site-facing or patient recruitment roles.</li><li>
Strong understanding of ICH/GCP and regulatory guidelines.</li><li>
Experience with patient recruitment workflows and site operations.</li><li>
Proficiency in Microsoft Office and remote collaboration tools (e.g., Teams).</li><li>
Excellent communication, training, and interpersonal skills.</li><li>
Strong organizational and time management abilities.</li><li>
Preferred: Experience in candidate selection and people management; familiarity with site contracting processes.</li><li>
Certifications such as CCRC (ACRP) or CCRP (SoCRA) are a plus.</li></ul><div><b>
Why IQVIA?</b><br>
Join a global leader driving innovation in clinical trial delivery. At IQVIA, you&rsquo;ll help sites accelerate patient recruitment, improve data quality, and reduce study fatigue&mdash;ultimately improving outcomes for patients and sponsors alike. We offer flexibility, continuous learning, and the opportunity to make an impact that matters.</div><div><b>
Ready to lead the way?</b><br>
 and be part of IQVIA&rsquo;s mission to advance human health.</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>

Site Enablement Lead & Site-Facing Line Manager

<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>


Clinical Trials Assistant (Single Sponsor) Turkey

Explore 652+ Senior clinical research associate sponsor dedicated t rkiye in Istanbul this December. Find roles across top companies and apply now to boost your career.