project specialist

site identification specialist (feasibility) Jobs in Ankara

site identification specialist (feasibility)

site reliability engineer

site specialist i, study start up (turkey, ankara) Jobs in Ankara

site specialist i, study start up (turkey, ankara)

site specialist ii, study start up Jobs in Ankara

site specialist ii, study start up

site identification specialist feasibility

PSI CRO

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 We are the company that cares &ndash; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.
 <br/>
 <br/>
 <strong>
  General Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
  </li>
  <li>
   Participate in the development and implementation of improvement strategies for the site identification process and related training activities
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Project Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Define the main study objectives and the optimal site profile
  </li>
  <li>
   Create initial list of potential sites
  </li>
  <li>
   Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
  </li>
  <li>
   In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
  </li>
  <li>
   Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
  </li>
  <li>
   In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
  </li>
  <li>
   Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University/college degree (Life Sciences/Pharmacy/Healthcare field is a plus), or an equivalent combination of education, training and experience
  </li>
  <li>
   Minimum 2 years of prior experience in site identification/study startup activities or equivalent
  </li>
  <li>
   Full professional working proficiency in Turkish and English
  </li>
  <li>
   Understanding of Good Clinical Practice, local laws and applicable regulations in Turkey
  </li>
  <li>
   Communication and collaboration skills
  </li>
  <li>
   Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.
</div>


Site Identification Specialist (Feasibility)

<div><b>Company Description</b><p><br>
We are the company that cares &ndash; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.</p><b><br>
Job Description</b><p><br>
We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.</p><p><b>
General Responsibilities:</b></p><ul><li>
Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement</li><li>
Participate in the development and implementation of improvement strategies for the site identification process and related training activities</li></ul><p><b>
Project Responsibilities:</b></p><ul><li>
Define the main study objectives and the optimal site profile</li><li>
Create initial list of potential sites</li><li>
Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use</li><li>
In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities</li><li>
Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives</li><li>
In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites</li><li>
Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed</li></ul><br>
<b>
Qualifications</b><br>
<ul><li>
University/college degree (Life Sciences/Pharmacy/Healthcare field is a plus), or an equivalent combination of education, training and experience</li><li>
Minimum 2 years of prior experience in site identification/study startup activities or equivalent</li><li>
Full professional working proficiency in Turkish and English</li><li>
Understanding of Good Clinical Practice, local laws and applicable regulations in Turkey</li><li>
Communication and collaboration skills</li><li>
Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements</li></ul><br>
<b>
Additional Information</b><p><br>
Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.</p></div>

Baker Hughes

<div><div><b>Lead Sourcing Specialist</b></div><div><div><div><div><div><div><div><div><div><h1 class="jobSectionHeader"><b>
Would you like the opportunity to be responsible for business growth?</b></h1><h1 class="jobSectionHeader"><b>
Would you like to be part of a new era?</b></h1><p></p><p><b>
Join our Team</b></p><p>
At Baker Hughes our purpose is clear. We take energy forward &ndash; making it safer, cleaner and more efficient for people and the planet.</p><p></p><p><b>
Partner with the best</b></p><p>
As a Lead Sourcing Specialist, you will negotiate with dedicated providers according to specific policies. You will ensure to achieve the best contractual conditions while also ensuring internal customer satisfaction.</p></div></div></div></div></div></div></div></div></div><p></p><p>
This position is open for pipelining purposes for an expected opening</p><p></p><p><b>
As a Lead Sourcing Specialist, you will be responsible for:</b></p><ul><li>
Manage all RFQs for a manufacturing or service site. Getting competitive offers while achieving the defined Deflation KPIs.</li><li>
Contribute in executing and implementation of Sourcing defined strategy for each commodity or Supplier.</li><li>
Work towards achieving specific defined KPIs set by product line.</li><li>
Define supplier strategy including management and optimization of supplier panels. Lead negotiations and allocate needs to specific suppliers. Negotiate terms and conditions and transmit information to Procurement. Manage claims. Includes commercial sourcing management such as data analysis, negotiations support, etc. This may also include purchasing activities.</li><li>
Detects and signals flaws in approaches, methods, procedures and processes and suggests improvements.</li><li>
Handles communication with direct colleagues and the business about data gathering and analysis.</li><li>
Negotiating best cost &amp; delivery, with suppliers; place and follow up on PO&rsquo;s for assigned commodities.</li><li>
Managing effective working relationships with suppliers for PO execution.</li><li>
Managing problems and schedule changes to ensure on time delivery.</li><li>
Updating ERP to ensure accurate planning.</li><li>
Developing new solutions under guidance and/or in a team setting.</li><li>
Balancing both tactical execution with strategic initiatives necessary to drive cost and lead time reduction.</li><li>
Working together with high level individuals within the business.</li><li>
Working with Commodity Buyers on technical and commercial developments to develop awareness of manufacturing processes and improve product knowledge</li></ul><p></p><p><b>
Fuel your passion</b></p><p><b>
To be successful in this role you will:</b></p><ul><li>
Have Bachelor's degree from an accredited university or college. (Engineering is preferred).</li><li>
Have a minimum of 6 years of experience in sourcing/procurement in the oil and gas industry.</li><li>
Knowledge of Ariba and SAP is an advantage.</li><li>
Have strong oral and written communication as well as interpersonal and leadership skills.</li><li>
Have the ability to lead initiatives of moderate scope and impact.</li><li>
Have effective problem identification and solution skills as well as proven analytical and organizational ability.</li></ul><p></p><p><b>
Work in a way that works for you</b></p><p>
We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer the following flexible working patterns:</p><ul><li><p>
Working flexible hours - flexing the times when you work in the day to help you fit everything in and work when you are the most productive</p></li></ul><p></p><p><b>
Working with us</b></p><p>
Our people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other.</p><p></p><p><b>
Working for you</b></p><p>
Our inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input. Join us, and you can expect:</p><ul><li><p>
Contemporary work-life balance policies and wellbeing activities</p></li><li><p>
Comprehensive private medical care options</p></li><li><p>
Safety net of life insurance and disability programs</p></li><li><p>
Tailored financial programs</p></li><li><p>
Additional elected or voluntary benefits</p></li></ul><p></p><b>
About Us:</b><div>
We are an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward &ndash; making it safer, cleaner and more efficient for people and the planet.</div><br>
<b>
Join Us:</b><div>
Are you seeking an opportunity to make a real difference in a company that values innovation and progress? Join us and become part of a team of people who will challenge and inspire you! Let&rsquo;s come together and take energy forward.<br>
<br>
Baker Hughes Company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.</div></div>

Lead Sourcing Specialist

INTEC Energy Solutions

<div>
 <p>
  INTEC Energy Solutions delivers best-in-class services in Engineering, Procurement, Construction (EPC), Battery Energy Storage Systems (BESS), Project Development, Consultancy, and Operation &amp; Maintenance, along with New Energy Solutions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  With a globally experienced team, INTEC has managed over 190 projects and achieved an impressive installed and secured capacity of 3.9 GW. Headquartered in the United Kingdom, INTEC also operates offices in Germany, T&uuml;rkiye, Australia, New Zealand, Azerbaijan, Romania, Mauritius, and Philippines with plans for further expansion.
 </p>
 <p>
  <br/>
 </p>
 <p>
  As an international company, we are looking for a
  <strong>
   Structural Design Engineer
  </strong>
  who will work in our T&uuml;rkiye office.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   QUALIFICATIONS AND JOB DESCRIPTION
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Description
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   The Civil &amp; Structural Design Engineer is responsible for performing and reviewing analysis and complete design calculations using the latest codes; prepare and manage the production of construction drawings, specifications, and engineering calculations. Client interaction and communication on projects will be expected.
  </li>
  <li>
   Creating structural engineering plans, details and calculations for Utility and Commercial scale solar projects in various regions with high wind, seismic and snow loads.
  </li>
  <li>
   Designing foundations for project equipment to meet jurisdictional requirements at local, State and Federal levels for various geotechnical parameters and soil types.
  </li>
  <li>
   Leading any site test (for instance Pull Out Test) and ensure that it is carried out according to relevant standards and client&rsquo;s requirements and expectations.
  </li>
  <li>
   Reviewing and responding to project construction administration items including Requests for Information (RFI), shop drawings, and submittals.
  </li>
  <li>
   Reviewing the designs of the EPCs to confirm compliance with the project requirements and code.
  </li>
  <li>
   Review and interpret site survey reports, such as geotechnical reports.
  </li>
  <li>
   Prepare in-house drawings which include all necessary technical specifications.
  </li>
  <li>
   Reading and understanding existing and proposed structural, architectural and civil drawings.
  </li>
  <li>
   Provide preliminary designs for feasibility study for special constructions/substructure.
  </li>
  <li>
   Compare and assess different methods/testing procedures for soil testing.
  </li>
  <li>
   Ability to interpret geotechnical reports and apply soil mechanics principles to foundation design &amp; structural design.
  </li>
  <li>
   Ability to manage time efficiently across multiple projects.
  </li>
  <li>
   Coordination with clients on their expectations.
  </li>
  <li>
   Gaining deep knowledge of PV system components such as modules, racking, inverters and Balance of Systems (BOS).
  </li>
  <li>
   Ability to work with and be supported by other engineers for guidance.
  </li>
  <li>
   Technical support to business development or sales team for tender, bidding or after sales technical support.
  </li>
  <li>
   Ensure compliance with company, industry, trade, and jurisdictional safety standards, practices, codes.
  </li>
  <li>
   Perform additional duties as assigned and/or directed.
  </li>
  <li>
   Design drainage systems, including ditches, culverts, and retention ponds, to manage rainwater and prevent water accumulation around equipment and structures.
  </li>
  <li>
   Develop erosion and sediment control plans to minimize environmental impact during construction.
  </li>
  <li>
   Conduct site visits during construction to monitor civil and structural works, ensuring adherence to design drawings, specifications, and quality standards.
  </li>
  <li>
   Address any site-related structural issues or design modifications that may arise during construction, providing timely solutions and clarifications.
  </li>
  <li>
   Perform inspections and quality checks on foundations, structural elements, and civil works to verify compliance and identify any defects.
  </li>
  <li>
   Coordination of external structural companies/engineers
  </li>
  <li>
   Act as a single point of contact / direct interface
  </li>
  <li>
   Preparation &amp; communication of scope of work for external structural companies/engineers
  </li>
  <li>
   Evaluation of proposals from external structural companies/engineers (tender phase)
  </li>
  <li>
   Preliminary structural analysis for feasibility study for special constructions/substructures
  </li>
  <li>
   Evaluation and optimization of substructure designs received from external companies
  </li>
  <li>
   Evaluation and optimization of determination of embedding pile length
  </li>
  <li>
   Dimensioning of reinforced concrete foundations
  </li>
  <li>
   Developing detailed layouts and civil design packages that meet all contractual, code, and permitting requirements
  </li>
  <li>
   Assessment of load assumptions/combinations for specific locations
  </li>
  <li>
   Assessment of structural calculation of precast / in-situ concrete foundations for transformer / collector stations
  </li>
  <li>
   Conducting on-site solar PV Parks site visit, commissioning and troubleshooting
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Qualifications
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Experienced in concrete &amp; steel structure design (both foundation and superstructure design)
  </li>
  <li>
   Well experienced on international well-known design standards (American codes and Euronorms and knowledge of AS/NZS norms is a plus)
  </li>
  <li>
   Experience in designing Structural Design Part of PV projects in large scale
  </li>
  <li>
   Well experienced on Autocad 2D &amp; Revit usage
  </li>
  <li>
   Well experienced on Tekla usage
  </li>
  <li>
   Well experienced in SAP2000, ETABS and Idea-statica
  </li>
  <li>
   Well experienced in structural design calculations &amp; reporting &amp; giving necessary design outputs for formwork &amp; rebar detailing works
  </li>
  <li>
   Be familiar to work in multi-discipline projects
  </li>
  <li>
   Having planning &amp; organization &amp; multitask skills, reporting,
  </li>
  <li>
   Compatible with managers and colleagues, helpful and hardworking
  </li>
  <li>
   Good level of English
  </li>
 </ul>
 <p>
 </p>
</div>


Structural Design Engineer

PharmEng Technology

<div>
 <strong>
  About The Job Quality Assurance Consultant
  <br/>
  <br/>
 </strong>
 <strong>
  Job Summary:
 </strong>
 The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   QMS implementation, maintenance, and oversight in local affiliates.
  </li>
  <li>
   Maintenance of the local Quality Manual and Site Master File.
  </li>
  <li>
   Quality risk management in local affiliate, including risk identification, analysis, communication, control, and escalation as required.
  </li>
  <li>
   Complaint management, acting as the Local Complaint Coordinator for reporting, local assessment, and local investigation.
  </li>
  <li>
   Change control management, QA assessment, site change control, QA review for change implementation and closure.
  </li>
  <li>
   Deviation management for internal, external, and transport deviations.
  </li>
  <li>
   CAPA management from deviations, internal audits, external audits, and self-inspections.
  </li>
  <li>
   Management of authority inspections and self-inspections.
  </li>
  <li>
   Local GxP surveillance and assessment.
  </li>
  <li>
   Product quality review (PQR).
  </li>
  <li>
   Training management, including maintenance of training matrix, training of local staff, annual GxP refresher training, and handling of training assignments in the LMS.
  </li>
  <li>
   Local product release (local QP), shipment review of transport performance, goods receipt check, and deviation handling.
  </li>
  <li>
   Oversight of GDP requirements for local warehousing and distribution.
  </li>
  <li>
   Shipping lane qualification and local transport performance of secondary distribution.
  </li>
  <li>
   Secondary distribution transport performance review.
  </li>
  <li>
   Return management, including QA evaluation against return criteria and collaboration with distributors.
  </li>
  <li>
   Product recall management, including local recall execution, communication with customers, communication with HA, recall reconciliation, and local product destruction.
  </li>
  <li>
   GxP suppliers management, including supplier identification, qualification, approval, annual compliance status evaluation, quality audit planning, conduct quality audits, and CAPA approval and closure.
  </li>
  <li>
   Local repackaging and relabeling, including change management, protocol, execution, QA review, and release.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Quality Management, Life Sciences, or a related field.
  </li>
  <li>
   Minimum of 5 years of experience in Quality Assurance within the pharmaceutical or healthcare industry.
  </li>
  <li>
   Strong knowledge of GxP regulations and quality standards.
  </li>
  <li>
   Excellent analytical, problem-solving, and communication skills.
  </li>
  <li>
   Ability to work independently and collaboratively in a team environment.
  </li>
  <li>
   Proficiency in using Quality Management Systems and Learning Management Systems (LMS).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Attention to detail and accuracy.
  </li>
  <li>
   Strong organizational and time management skills.
  </li>
  <li>
   Effective leadership and team management abilities.
  </li>
  <li>
   Proactive and results-oriented mindset.
  </li>
 </ul>
</div>


Quality Assurance Consultant

<div>
 <strong>
  Would you like the opportunity to be responsible for business growth?
  <br/>
  <br/>
 </strong>
 <strong>
  Would you like to be part of a new era?
  <br/>
  <br/>
 </strong>
 <strong>
  Join our Team
  <br/>
  <br/>
 </strong>
 At Baker Hughes our purpose is clear. We take energy forward &ndash; making it safer, cleaner and more efficient for people and the planet.
 <br/>
 <br/>
 <strong>
  Partner with the best
  <br/>
  <br/>
 </strong>
 As a Lead Sourcing Specialist, you will negotiate with dedicated providers according to specific policies. You will ensure to achieve the best contractual conditions while also ensuring internal customer satisfaction.
 <br/>
 <br/>
 This position is open for pipelining purposes for an expected opening
 <br/>
 <br/>
 <strong>
  As a Lead Sourcing Specialist, you will be responsible for:
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Manage all RFQs for a manufacturing or service site. Getting competitive offers while achieving the defined Deflation KPIs.
  </li>
  <li>
   Contribute in executing and implementation of Sourcing defined strategy for each commodity or Supplier.
  </li>
  <li>
   Work towards achieving specific defined KPIs set by product line.
  </li>
  <li>
   Define supplier strategy including management and optimization of supplier panels. Lead negotiations and allocate needs to specific suppliers. Negotiate terms and conditions and transmit information to Procurement. Manage claims. Includes commercial sourcing management such as data analysis, negotiations support, etc. This may also include purchasing activities.
  </li>
  <li>
   Detects and signals flaws in approaches, methods, procedures and processes and suggests improvements.
  </li>
  <li>
   Handles communication with direct colleagues and the business about data gathering and analysis.
  </li>
  <li>
   Negotiating best cost &amp; delivery, with suppliers; place and follow up on PO&rsquo;s for assigned commodities.
  </li>
  <li>
   Managing effective working relationships with suppliers for PO execution.
  </li>
  <li>
   Managing problems and schedule changes to ensure on time delivery.
  </li>
  <li>
   Updating ERP to ensure accurate planning.
  </li>
  <li>
   Developing new solutions under guidance and/or in a team setting.
  </li>
  <li>
   Balancing both tactical execution with strategic initiatives necessary to drive cost and lead time reduction.
  </li>
  <li>
   Working together with high level individuals within the business.
  </li>
  <li>
   Working with Commodity Buyers on technical and commercial developments to develop awareness of manufacturing processes and improve product knowledge
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Fuel your passion
  <br/>
  <br/>
 </strong>
 <strong>
  To be successful in this role you will:
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Have Bachelor's degree from an accredited university or college. (Engineering is preferred).
  </li>
  <li>
   Have a minimum of 6 years of experience in sourcing/procurement in the oil and gas industry.
  </li>
  <li>
   Knowledge of Ariba and SAP is an advantage.
  </li>
  <li>
   Have strong oral and written communication as well as interpersonal and leadership skills.
  </li>
  <li>
   Have the ability to lead initiatives of moderate scope and impact.
  </li>
  <li>
   Have effective problem identification and solution skills as well as proven analytical and organizational ability.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work in a way that works for you
  <br/>
  <br/>
 </strong>
 We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer the following flexible working patterns:
 <br/>
 <br/>
 <br/>
 <ul>
  <li>
   Working flexible hours - flexing the times when you work in the day to help you fit everything in and work when you are the most productive
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Working with us
  <br/>
  <br/>
 </strong>
 Our people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other.
 <br/>
 <br/>
 <strong>
  Working for you
  <br/>
  <br/>
 </strong>
 Our inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input. Join us, and you can expect:
 <br/>
 <br/>
 <br/>
 <ul>
  <li>
   Contemporary work-life balance policies and wellbeing activities
  </li>
  <li>
   Comprehensive private medical care options
  </li>
  <li>
   Safety net of life insurance and disability programs
  </li>
  <li>
   Tailored financial programs
  </li>
  <li>
   Additional elected or voluntary benefits
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About Us:
  <br/>
  <br/>
 </strong>
 We are an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward &ndash; making it safer, cleaner and more efficient for people and the planet.
 <br/>
 <br/>
 <strong>
  Join Us:
  <br/>
  <br/>
 </strong>
 Are you seeking an opportunity to make a real difference in a company that values innovation and progress? Join us and become part of a team of people who will challenge and inspire you! Let&rsquo;s come together and take energy forward.
 <br/>
 <br/>
 Baker Hughes Company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
 <br/>
 <br/>
 <strong>
  R156776
 </strong>
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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

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