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site contracts negotiator ii

ICON plc

<div>Site Contracts Negotiator 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>
The Role</div><div>
In this position, you will be responsible for negotiating and finalising Clinical Trial Agreements and amendments with sites across Turkey. You will work closely with local site teams and ICON&rsquo;s internal stakeholders to remove contracting barriers, protect ICON and client interests, and ensure studies progress according to planned timelines. Your ability to communicate clearly in both Turkish and English, manage risks, and maintain accurate contract documentation will be key to delivering successful site activation.</div><div></div><div>
Key Responsibilities:</div><ul><li><div>
Negotiate and finalise CTAs and amendments with Turkish sites to enable timely site activation while ensuring full compliance with Turkish legislation, ICON SOPs, and client requirements.</div></li><li><div>
Act as the primary contracting contact for Turkish sites, building strong relationships and ensuring clear, culturally appropriate communication throughout the contracting process.</div></li><li><div>
Maintain proactive communication with internal teams to keep study stakeholders aligned on contracting progress, risks, and expected timelines.</div></li><li><div>
Track the status of all contracts in ICON and client systems so that study teams have accurate visibility and can plan start-up activities effectively.</div></li><li><div>
Identify potential risks or delays early and propose realistic mitigation strategies to protect study timelines.</div></li><li><div>
Review all contract documents for accuracy and compliance, ensuring that agreements meet legal, financial, and operational standards specific to Turkey.</div></li><li><div>
Collaborate cross-functionally with SSU, Legal, Regulatory, and Clinical Operations to ensure contract terms reflect site requirements and support smooth initiation.</div></li><li><div>
Participate in study calls and internal meetings to align contracting work with overall study goals.</div></li><li><div>
Maintain organised, audit-ready contract files in accordance with ICON and client requirements.</div></li><li><div>
Support continuous improvement initiatives within the department and provide mentorship when needed.</div></li><li><div>
Complete mandatory training and adhere to SOPs to ensure consistent, high-quality delivery.</div></li></ul><div></div><div>
What You Need</div><ul><li><div>
Bachelor&rsquo;s degree.</div></li><li><div>
3&ndash;6 years of experience in clinical research, site contracts, or a related field.</div></li><li><div>
Fluency in both Turkish and English (written and spoken) is essential.</div></li><li><div>
Strong understanding of Turkish site contracting practices and local regulatory expectations.</div></li><li><div>
Excellent communication and relationship-building skills with both internal teams and investigative sites.</div></li><li><div>
Strong organisational skills and the ability to independently manage multiple priorities.</div></li><li><div>
High attention to detail and confidence in managing site-facing negotiations.</div></li></ul><div></div><div>
#LI-MK1</div><div>
#LI-Remote</div><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 Contracts Negotiator 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>
  The Role
  <br/>
  <br/>
 </strong>
 In this position, you will be responsible for negotiating and finalising Clinical Trial Agreements and amendments with sites across Turkey. You will work closely with local site teams and ICON&rsquo;s internal stakeholders to remove contracting barriers, protect ICON and client interests, and ensure studies progress according to planned timelines. Your ability to communicate clearly in both Turkish and English, manage risks, and maintain accurate contract documentation will be key to delivering successful site activation.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Negotiate and finalise CTAs and amendments with Turkish sites to enable timely site activation while ensuring full compliance with Turkish legislation, ICON SOPs, and client requirements.
  </li>
  <li>
   Act as the primary contracting contact for Turkish sites, building strong relationships and ensuring clear, culturally appropriate communication throughout the contracting process.
  </li>
  <li>
   Maintain proactive communication with internal teams to keep study stakeholders aligned on contracting progress, risks, and expected timelines.
  </li>
  <li>
   Track the status of all contracts in ICON and client systems so that study teams have accurate visibility and can plan start-up activities effectively.
  </li>
  <li>
   Identify potential risks or delays early and propose realistic mitigation strategies to protect study timelines.
  </li>
  <li>
   Review all contract documents for accuracy and compliance, ensuring that agreements meet legal, financial, and operational standards specific to Turkey.
  </li>
  <li>
   Collaborate cross-functionally with SSU, Legal, Regulatory, and Clinical Operations to ensure contract terms reflect site requirements and support smooth initiation.
  </li>
  <li>
   Participate in study calls and internal meetings to align contracting work with overall study goals.
  </li>
  <li>
   Maintain organised, audit-ready contract files in accordance with ICON and client requirements.
  </li>
  <li>
   Support continuous improvement initiatives within the department and provide mentorship when needed.
  </li>
  <li>
   Complete mandatory training and adhere to SOPs to ensure consistent, high-quality delivery.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Need
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree.
  </li>
  <li>
   3&ndash;6 years of experience in clinical research, site contracts, or a related field.
  </li>
  <li>
   Fluency in both Turkish and English (written and spoken) is essential.
  </li>
  <li>
   Strong understanding of Turkish site contracting practices and local regulatory expectations.
  </li>
  <li>
   Excellent communication and relationship-building skills with both internal teams and investigative sites.
  </li>
  <li>
   Strong organisational skills and the ability to independently manage multiple priorities.
  </li>
  <li>
   High attention to detail and confidence in managing site-facing negotiations.
   <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>


<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>

Senior Clinical Research Associate

Halliburton

<div><p>We are looking for the right people &mdash; people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and their careers. Experience the challenges, rewards and opportunity of working for one of the world&rsquo;s largest providers of products and services to the global energy industry.</p><div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><p></p><div><p><b><br>
JOB DESCRIPTION:</b></p><br>
<p></p><ul><li>
Under general supervision, performs all phases of the rigging up/down of Subsea Safety Systems (SSS) service line equipment on work locations for the purpose of maintaining control of wellbore fluids and providing means for well intervention and interfacing during well testing operations, by the use of (but not limited to): Subsea Well Control equipment.</li><li>
Regularly works within other Testing and Subsea (TSS) product service lines on location and in the workshop.</li><li>
Routinely works in more than one type of well site (onshore/offshore) and base camp as assigned by Service Coordinator.</li><li>
Coordinates and oversees SSS service line functions at the well site and field camp.</li><li>
Provides the planning necessary for the job including equipment set up, well site direction, and customer-related support activities.</li><li>
Responsible for the activities relative to maintaining, setting up, testing, and operating equipment at the customer location and field camp.</li><li>
Provides basic customer reports.</li><li>
Mentors/trains lower level Service Operators in areas of expertise.</li><li>
May be designated to become an Assessor for junior SSS personnel.</li><li>
Monitors instruments/performs necessary calculations to assure quality of data/job.</li><li>
Consults with customers concerning services and products, promotes good customer relations at the well site, and assures customer satisfaction with results.</li><li>
Properly maintains assigned equipment and monitors compliance with safety regulations and procedures.</li><li>
Conducts pre-job toolbox safety meetings, reviews and verifies job plan with customer representative and manages any changes required.</li><li>
Checks and verifies equipment as per job plan, completes all job documentation to include: Job Ticket, Job History Report, CV Metrics/KPI, Job Log, Job Summary etc.</li><li>
Demonstrates understanding of down hole hydraulics, including basic job calculations, working knowledge of Blow Out Prevention (BOP) function and of basic reservoir &ndash; i.e., BHP, BHT, hydrocarbon characteristics.</li><li>
Job tasks, correctly performed, impact indirectly on cost containment, efficiency, profitability of operations.</li><li>
Skills typically acquired through completion of high school or similar education and 4 years of SSS experience.</li><li>
Must have successfully passed company tests or met task guideline requirements.</li><li>
Must meet the minimum competency requirements for the Service Operator II&ndash;SSS.</li><li>
Must be knowledgable in most aspects of SSS service line in the local area.</li><li>
Must be able to interpret Tool Engineering Drawings and interpret basic pressure/temperature vs. time plots.</li><li>
Must be able to pressure test equipment safely.</li><li>
Must have demonstrated knowledge of basic rig function including, but not limited to the following: a) Weight Indicator - What is it used for, and how it relates to our work;. b) Mud System - Weights of common well fluids - what effect they can have on our equipment; c) Limitations of mud pumps, pressure reading, strokes per/min - bbls/min.; and d) Basic rig manifold.</li><li>
Excellent leadership and communication skills are required.</li><li>
Must be able to use Correction, Prevention, and Improvement (CPI) System to document problems encountered or ideas for improvement.</li><li>
Good math and computer skills required.</li><li>
Good reading comprehension and writing skills required.</li><li>
Must be capable of understanding/navigating HMS, iLearn and Competency sites on HalWorld.</li><li>
local knowledge and language preferred.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Qualifications</b></h2></div></div></div><div></div><p><b>
Halliburton is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation</b>.</p><p></p><p><b><br>
Location</b></p><p>
Bestepe, Yasam Cad. 13A-77, Ankara, Ankara, 06560, T&uuml;rkiye</p><p></p><p><b><br>
Job Details</b></p><p><b>
Requisition Number:</b> 202815
<br>
<b>Experience Level: </b>Entry-Level<br>
<b>Job Family:</b> Operations<br>
<b>Product Service Line: </b>Testing and Subsea
<br>
<b>Full Time / Part Time: </b>Full Time</p><p><b>
Additional Locations for this position:</b></p><p></p><p><b><br>
Compensation Information</b><br>
Compensation is competitive and commensurate with experience.</p></div>

Service Specialist I-Subsea Safety Systems - Ankara

<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><p>We are looking for the right people &mdash; people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and their careers. Experience the challenges, rewards and opportunity of working for one of the world&rsquo;s largest providers of products and services to the global energy industry.</p><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Job Duties</b></h2></div><p></p><div><p><b><br>
JOB DESCRIPTION:</b></p><br>
<p></p><ul><li>
Under general supervision, coordinates and oversees Testing &amp; Subsea (TSS) Subsea Safety Systems (SSS) product service line (PSL) work at the well site, providing excellent customer relations at the worksite during well testing or other type operaton.</li><li>
Plans and performs necessary calculations for the total job at the well site as needed.</li><li>
Coordinates and directs the activities of service operators during the equipment rig up/rig down on a location and the preparation of equipment for performing a job.</li><li>
Provides planning necessary for the job including instructions to the crew and equipment used, including dispute resolutions to approved levels.</li><li>
Recognizes possible sales opportunities for the Company's other products and service and communicates information to Service Coordinator or appropriate Company staff.</li><li>
Ensures customer satisfaction with jobs performed.</li><li>
As needed, may perform data collection and data distribution on jobs.</li><li>
Coordinates the clean up, repair, and preparation of equipment for the next job.</li><li>
Provides coaching and input on individual performance levels of his/her subordinates providing on-the-job skills development to enhance job performance.</li><li>
Leads by example.</li><li>
Must be capable of navigating/utilizing HMS, iLearn and Competency sites on HalWorld.</li><li>
Will be required to become a dedicated Assessor for junior SSS personnel.</li><li>
Must possess exceptional skills within the service line and have a general understanding of other service functions.</li><li>
 Promotes HES Process Improvement Initiatives (PII) within the assiged Country or Natural Work Area (NWA).</li><li>
Ensures compliance with Health, Safety, and Environmental (HSE) standards, practices and guidelines.</li><li>
Must posses execellent knowledge of Halliburton Management System (HMS) standards, work methods and processes.</li><li>
Demonstrates understanding of downhole hydraulics, including basic job calculations, working knowledge of wireline Blow Out Prevention (BOP) function and of basic reservoir&ndash;i.e., BHP, BHT, hydrocarbon characteristics.</li><li>
Promotes and takes an active part in quality improvement processes.</li><li>
Coaches individuals for better performance and promotes high morale.</li><li>
Job tasks, correctly performed, impact indirectly on cost containment, efficiency, profitability of operations.</li><li>
Skills are typically acquired through a high school diploma or similar education and 1 year of experience as Service Specialist I&ndash;SSS or 5 years of SSS experience including the role as a supervisor.</li><li>
Must have successfully passed company tests or met task guideline requirements.</li><li>
Must meet the minimum competency requirements for the Service Operator II&ndash;SSS. Should be fully knowledgeable in most aspects of SSS service line in the local area.</li><li>
Actively pursues self development. Leads by example.</li><li>
Ability to communicate with team and customer to affect knowledge transfer relate to job plans, calculations, well parameters, specific hazards, environmental issues, quality service, equipment, etc related to the job. Math and computer skills required.</li><li>
The ability to communicate effectively with others is necessary.</li><li>
Commitment to company and customer safety performance. Ability to discuss future work opportunities with customer.</li><li>
Must be able to explain the local HMS process for Prepare Resources.</li><li>
Must be able to use Correction, Prevention and Improvement (CPI) System to document problems encountered or ideas for improvement.</li><li>
Must have completed supervisory training. Licensure to drive commercial vehicles may be required.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Qualifications</b></h2></div></div></div><p></p><p><b><br>
Halliburton is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation</b>.</p><p></p><p><b><br>
Location</b></p><p>
Bestepe, Yasam Cad. 13A-77, Ankara, Ankara, 06560, T&uuml;rkiye</p><p></p><p><b><br>
Job Details</b></p><p><b>
Requisition Number:</b> 204051
<br>
<b>Experience Level: </b>Experienced Hire<br>
<b>Job Family:</b> Operations<br>
<b>Product Service Line: </b>[[division]]
<br>
<b>Full Time / Part Time: </b>Full Time</p><p><b>
Additional Locations for this position:</b></p><p></p><p><b><br>
Compensation Information</b><br>
Compensation is competitive and commensurate with experience.</p></div>

Service Supervisor I -Subsea Safety Sys

Explore 69+ Site contracts negotiator ii in Ankara this January. Find roles across top companies and apply now to boost your career.

69 site contracts negotiator ii jobs IN Ankara

Site Contracts Negotiator II

Site Contracts Negotiator II

Site Specialist II, Study Start Up

Senior Clinical Research Associate

Service Specialist I-Subsea Safety Systems - Ankara

Site Specialist II

Service Supervisor I -Subsea Safety Sys