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clinical research associate ii

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customer service specialist

regulatory affairs 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>Site Specialist II<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
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

<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/>
 <strong>
  What You Will Be Doing
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
  </li>
  <li>
   Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
  </li>
  <li>
   Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence
  </li>
  <li>
   Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.
  </li>
  <li>
   Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your profile
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in life sciences or a related field.
  </li>
  <li>
   Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.
  </li>
  <li>
   Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.
  </li>
  <li>
   Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
  </li>
  <li>
   Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
   <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
</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)

<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/>
 <strong>
  What you will be doing?
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Collaborate with key stakeholders to manage and complete data entry and document upload to and monitoring of Clinical Trial Regulatory systems/portals according to study specifics, ICON policies, procedures, applicable regulations and the principles of ICH-GCP with in line with contractual agreement
  </li>
  <li>
   Support Regulatory submissions and deliverables to meet department and project goals
  </li>
  <li>
   Depending upon experience, become involved, when required, staff training/mentoring and contribute to the review of ICON systems and procedures as appropriate
  </li>
  <li>
   As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs
  </li>
  <li>
   Ensure Regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget
  </li>
  <li>
   Thorough knowledge of ICON&rsquo;s SOPs/WIs, ICH, GCP, appropriate regulations and guidance
  </li>
  <li>
   Thorough knowledge of ICON systems applicable to role
  </li>
  <li>
   Proactively identify and mitigate risks through Regulatory Agency helpdesks or internal sources, regarding data/document management and upload to Clinical Trial Regulatory systems/portals and liaise with internal/external stakeholders to resolve
  </li>
  <li>
   Actively maintain applicable study-level account access for assigned projects for Clinical Trial Regulatory systems/portals to maintain compliance and confidentiality
  </li>
  <li>
   Collaborate with key stakeholders to manage and perform data entry and document upload to required country/regional Regulatory systems/portals using the data and documents provided by project team
  </li>
  <li>
   Monitor Clinical Trial Regulatory systems/portals for notices and alerts and notifying applicable stakeholders of activities for their action and subsequent follow up
  </li>
  <li>
   Create files documenting submissions completed through country/regional Clinical Trial Regulatory systems/portals, conclusions, decisions and any other communication provided via Clinical Trial Regulatory systems/portals
  </li>
  <li>
   Perform Quality Control review in accordance with applicable process
  </li>
  <li>
   Maintain agreed timelines
  </li>
  <li>
   Support other Regulatory deliverables under the direction of leadership, as required
  </li>
  <li>
   Travel (approximately 5%) domestic and /or international
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your profile
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum of 3 years&rsquo; relevant experience
  </li>
  <li>
   Read, write and speak fluent English
  </li>
  <li>
   Proficient in using applicable business applications
   <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>


Senior Regulatory Technician

GE HealthCare

<div>
 <strong>
  Job Description Summary
  <br/>
  <br/>
 </strong>
 Service Delivery Specialist is responsible for managing logistics process, service parts ordering, and delivery process, service tools management and logistics operation excellence across Iran business and Turkiye indirect channel partners. Responsibility to manage service delivery process and transportation related logistics of goods and services to and from internal and/or external customers/suppliers for Iran and channel partners. Driving service delivery to ensure customer satisfaction, problem resolution and operation excellence across Iran business and channel partners.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Roles and Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Oversee customs clearance and regulatory processes specific to Iran business, ensuring compliance with all applicable international sanctions and trade laws.
  </li>
  <li>
   Develop and lead end-to-end logistics solutions to achieve required on-time pick up &amp; delivery of goods.
  </li>
  <li>
   Manage Logistics Costs to meet budgets and Op Plans.
  </li>
  <li>
   Follow up custom clearness and regulatory process of Iran business.
  </li>
  <li>
   Developing in-depth knowledge of a technical discipline. Uses prior experience and acquired technical expertise to execute policy/strategy.
  </li>
  <li>
   In-depth understanding of key business drivers; uses this understanding to accomplish own work.
  </li>
  <li>
   In-depth understanding of how work of own team integrates with other teams and contributes to the area.
  </li>
  <li>
   Uses some level of judgment and has ability to propose different solutions outside of set parameters but with guidance.
  </li>
  <li>
   Uses prior experience and on-the-job training to solve straightforward tasks.
  </li>
  <li>
   Has access to technical skills and analytic thinking required to solve problems.
  </li>
  <li>
   May use multiple internal sources outside of own team to arrive at decisions.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Logistics, Supply Chain Management, or related field (or equivalent experience).
  </li>
  <li>
   3&ndash;5 years of professional experience in logistics operations and compliance.
  </li>
  <li>
   Strong understanding of international logistics processes and regulatory requirements.
  </li>
  <li>
   Proven ability to work within complex regulatory environments, specifically related to Iran sanctions.
  </li>
  <li>
   Familiarity with OFAC, EU, and local regulations impacting Iran trade.
  </li>
  <li>
   Strong command of English, both written and verbal. (Knowledge of Arabic or Persian is desirable.)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   <strong>
    Additional Information
    <br/>
    <br/>
   </strong>
  </strong>
 </strong>
 <strong>
  Relocation Assistance Provided:
 </strong>
 No
</div>


Service Delivery Specialist

MINDPICKED

<div>
 <p>
  MINDPICKED is a new generation recruitment firm providing companies solutions in their search for talent, and talents opportunities to reach their potential.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We specialize in middle and senior management recruitment in various sectors and countless job functions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are looking for a
  <strong>
   Procurement Specialist
  </strong>
  for our client. Our client is a leading company in the energy sector.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Business Administration, International Trade, or a related field,
  </li>
  <li>
   Minimum 3 years of experience in procurement or supply chain operations,
  </li>
  <li>
   Proven experience with SAP ERP systems,
  </li>
  <li>
   Solid understanding of procurement processes, vendor management, and stock/material flow,
  </li>
  <li>
   Good command of English,
  </li>
  <li>
   Strong negotiation, organization, and communication skills,
  </li>
  <li>
   Analytical thinking and result-oriented mindset,
  </li>
  <li>
   Ability to work in a dynamic, fast-paced production environment.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Manage and execute procurement operations, including supplier sourcing, quotation analysis, and purchase order processing,
  </li>
  <li>
   Monitor critical stock levels and ensure timely procurement according to company policies,
  </li>
  <li>
   Maintain and update approved supplier lists, and evaluate new suppliers for potential inclusion,
  </li>
  <li>
   Execute purchases of approved materials and services, ensuring delivery according to required timelines,
  </li>
  <li>
   Prepare procurement-related documentation, draft service contracts, and obtain necessary approvals from legal and relevant departments,
  </li>
  <li>
   Coordinate with planning, production, quality, warehouse, and finance departments to align procurement with operational needs,
  </li>
  <li>
   Participate in acceptance processes for materials and services when necessary,
  </li>
  <li>
   Track KPIs, maintain reporting, and ensure compliance with procurement policies and regulatory requirements,
  </li>
  <li>
   Suggest improvements to increase efficiency, reduce costs, and enhance quality,
  </li>
  <li>
   Ensure compliance with occupational health &amp; safety, environmental, and sustainability standards.
  </li>
 </ul>
</div>


Procurement Specialist

Explore 50+ Regulatory affairs specialist in Ankara this December. Find roles across top companies and apply now to boost your career.

50 regulatory affairs specialist jobs IN Ankara

Site Specialist II, Study Start Up

Site Specialist II

Site Specialist II

Senior Clinical Research Associate (Contract)

Senior Regulatory Technician

Service Delivery Specialist

Procurement Specialist