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country study specialist senior cra

RAY CRO

<p><b>Main Responsibilities and Accountabilities:</b></p><p>&middot; Coordinates/supports operational aspects for implementation of clinical trial activities from study start-up through database lock, ensuring quality and safety standards, regulations, timelines and budget commitments are met.</p><p>&middot; Performs/coordinates protocol and site level feasibility activities, including evaluation of patient population and final site selection (if applicable).</p><p>&middot; Provides input into and/or develops study related materials such as Monitoring Plans, Recruitment Plans and Study Newsletters.</p><p>&middot; Supports/coordinates the negotiation of site budgets within Fair Market Value (FMV) guidelines, budget plans and provides oversight for site payments per contract, as required.</p><p>&middot; Maintains effective and ongoing communication with CSM; supports communication with local study teams and to sites as required.</p><p>&middot; Works with the global study team and CSM to manage or support the day-to-day activities of the study, including monitoring reports review, problem solving, issue escalation, timely closure of non-productive sites and tracking of safety procedures.</p><p>&middot; Supports management of country-level Trial Master File (TMF) and reviews for quality (including translations, as applicable).</p><p>&middot; Is responsible for the co-ordination and oversight of hub/country level audit/inspection action plan activities.</p><p>&middot; Updates knowledge on related regulatory requirements, ensures adherence and compliance with local regulations and internal procedures.</p><p>&middot; Executes all start-up activities prior to site activation on assigned studies, according to company standards and aligned with study/project requirements and timelines.</p><p>&middot; Prepares country and/or site Informed Consent Form (ICF) and clinical study documents which need translation from English into local language.</p><p>&middot; Maintains and analyzes study start-up data (metrics) on assigned studies, ensuring optimal efficiency to reduce start-up timelines and identify opportunities for continuous improvement.</p><p>&middot; Liaises and collaborates with relevant authorities/bodies to further enhance clinical trial process, government policies/ laws, via innovative approaches</p><p>&middot; Submits, where applicable and according to local regulatory requirements, all Suspected Unexpected Serious Adverse Reactions (SUSARs), Six Monthly SUSAR Reports (SSRs) and Development Safety Update Reports (DSURs) in collaboration with LSR.</p><p>&middot; Participates in study budget process and is responsible for contracts negotiation in collaboration with Business Support Leader and Country Study Manager, as required and ensures compliance with Fair Market Value (FMV) in the country.</p><p>Job Type: Full-time</p>

Country Study Specialist - Senior CRA

visuna

<div><p>Job Reference: 201555</p><div><br>
</div><div><div><div><p>Upstream
</p></div></div><p></p><div><div><b>Start Date: </b>01/04/2026</div><div><b>
Applications close on: </b>01/04/2026</div><div><b>
Contract Type: </b>Contract</div><div><b>
Country: </b>Kuwait</div><div><b>
Discipline: </b>IT and Software</div><div><b>
Job Contact: </b>louise.davies@visuna.com</div>
</div></div><p></p><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>Job Title: Senior IT Consultant</b></h2><br>
<p></p>
<div><b>Location:</b> Collaboration Center &ndash; Ahmadi &amp; NK</div>
<div><b>Industry:</b> Oil &amp; Gas / Large-Scale Projects</div>
<p></p>
<h3 class="jobSectionHeader"><b>Job Overview</b></h3><br>
<p>
The Senior IT Consultant will be responsible for managing, supporting, and optimizing IT systems, infrastructure, and technology operations for the Collaboration Center. Acting as the primary IT point of contact, this role ensures that all systems align with organizational standards while supporting seamless day-to-day operations. The position involves close coordination with internal teams, vendors, and stakeholders to ensure reliable, secure, and efficient IT services.</p>
<h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><br>
<ul>
<li><p>Manage and support the Collaboration Center&rsquo;s technology equipment and IT facilities (Ahmadi &amp; NK).</p>
</li>
<li><p>Oversee and coordinate third-party vendors for IT maintenance, support, and service delivery.</p>
</li>
<li><p>Serve as the primary IT focal point for the KwIDF project.</p>
</li>
<li><p>Manage project-related systems, including KwIDF servers and associated infrastructure.</p>
</li>
<li><p>Coordinate and communicate with multiple IT teams, business units, and project stakeholders.</p>
</li>
<li><p>Monitor system performance and implement upgrades, enhancements, or corrective actions as required.</p>
</li>
<li><p>Provide hands-on end-user support and technical assistance for both project and center operations.</p>
</li>
<li><p>Prepare technical documentation, reports, and updates for management and project stakeholders.</p>
</li>
<li><p>Ensure full compliance with IT governance frameworks, security standards, and organizational policies.</p></li></ul><p><br>
</p>
<h3 class="jobSectionHeader"><b>Required Qualifications &amp; Experience</b></h3><br>
<ul>
<li><p>Bachelor&rsquo;s degree in Information Technology or a related field.</p>
</li>
<li><p>Minimum of <b>10 years&rsquo; experience</b> in IT consulting, systems administration, and infrastructure management.</p>
</li>
<li><p>Strong hands-on experience with <b>hardware infrastructure and audiovisual (AV) systems</b>.</p>
</li>
<li><p>Proven experience supporting large-scale projects, collaboration centers, or operational facilities.</p>
</li>
</ul><h3 class="jobSectionHeader"><b>Good to Have</b></h3><br>
<ul>
<li><p>Prior experience working within the <b>oil and gas sector</b>.</p>
</li>
<li><p>Expertise in <b>enterprise data management</b>.</p>
</li>
<li><p>Experience working in multi-stakeholder, high-availability environments.</p>
</li>
</ul><p></p><h3 class="jobSectionHeader"><b>Benefit of Working with Visuna?
</b></h3><p></p><ul><li>A dedicated member of the team responsible for your placements and welfare</li>
<li>Some of the best day rates in the industry</li>
<li>FREE worldwide insurance and Medevac cover whist on a Placement</li>
<li>24/7 access to our specialist support team</li>
<li>Assistance and advice on a range of business topics</li>
<p></p>
<li>FREE access to our Competency Scheme</li>
<li>Increased exposure to potential clients and more placement opportunities</li></ul></div></div></div></div></div></div></div><p></p>

Senior IT Consultant

Kyong-Ho Engineering & Architects Co., Ltd.

<p><b>QUALIFICATIONS:</b></p><ul><li><b>Bachelor's degree or higher</b> in Civil Engineering of related field</li><li>Applicants must be a <b>registered/licensed Civil Engineer </b>or equivalent certificate/license issued by relevant authority of the country.</li><li>Candidates must have <b>at least five (5) years of experience as Capacity Development Specialist in Construction Supervision of Bridge/Highway projects</b> and at least <b>three (3) years of experience under FIDIC based Contract</b>, preferably Construction MDB Harmonized Edition.</li><li>Relevant trainings &amp; seminars are an advantage.</li><li><b>Must be willing to work overseas</b></li></ul><p>Job Type: Contract</p>

Sr. Capacity Development Specialist

<div>
 The Logistics Lead is responsible for executing and managing logistics operations for a country or basin, by finding a cost-efficient solution and ensuring maximum service level quality to field operations. The Logistics lead manages a team of logistics specialists, Import export specialists and logistics billing specialists.
 <br/>
 <br/>
 <ul>
  <li>
   Provides on-time logistics at a competitive cost to Operations.
  </li>
  <li>
   Manages logistics specialists, Import export specialists and logistics billing specialists, ensuring the proper training path is accomplished, assess their competencies and identifies learning opportunities.
  </li>
  <li>
   Ensures appropriate levels of support is given to internal/ external customers and works with the Logistics Manager to fill gaps.
  </li>
  <li>
   Serves as the first point of contact for the logistics operational issues.
  </li>
  <li>
   Implements and/ or supports logistics cost-saving initiatives.
  </li>
  <li>
   Ensures compliance of all services and transactions to all applicable SLB and regulatory guidelines (including but not limited to, land transport guidelines, HSE policies, local and international regulations and dangerous goods requirements).
  </li>
  <li>
   Ensure all Service Quality incidents are reported on time in QUEST and investigated when necessary.
  </li>
  <li>
   Ensure timely escalation of potential service quality failures to line management.
  </li>
  <li>
   Active involvement in reviewing and assessing the performance of logistics service providers through proactive engagement with Logistics Category/ Supplier Manager.
  </li>
  <li>
   Proactive engagement with internal customers via regular business/ service quality reviews.
  </li>
  <li>
   Ensure compliance of the team with internal procedures and management of deviations through proper change management protocol.
  </li>
  <li>
   Stays current with all safety training requirements.
  </li>
  <li>
   Is accountable for minimizing rental fleet idle time and optimizing truck capacity utilization.
  </li>
  <li>
   Works closely with Operations to develop Mobilization/Demobilization (Mob/Demob) Forecast.
  </li>
  <li>
   Works closely with Logistics specialist assigned to receive and execute the Mob/Demob plan.
  </li>
  <li>
   The Logistics Lead would normally have logistics specialists and / or Import export specialists and/or logistics billing specialists reporting into him/her. In case the Logistics Lead is based in the LCT he/she may also have Intercompany Process Coordinators reporting into him/her. The supervisor's reporting line is into GU Logistics manager or into the SSC organization where applicable / based on location of the role.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 The Logistics Supervisor would normally have logistics specialists and/or billing specialist reporting into him/her. In case the Logistics Supervisor is based in the LCT he/she may also have Intercompany Process Coordinators reporting into him/her. The supervisor's reporting line is into GU Logistcs manager or into the SSC organization where applicable / based on location of the role.
 <br/>
 <br/>
 <ul>
  <li>
   12 years Minimum Experiance
   <br/>
  </li>
 </ul>
</div>


Logistics Lead

AbbVie

<div><b>Company Description</b><p><br>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p><b><br>
Job Description</b><p><b><br>
Affiliate:</b></p><p><b>
Gulf Levant
</b></p><p><b>Title:</b></p><p><b>
Medical Advisor &ndash; Gastroenterology
</b></p><p><b>Reporting to:</b></p><p><b>
Medical Manager &ndash; Immunology
</b></p><p><b>PRIMARY FUNCTION:
</b></p><p>Represent the affiliate&rsquo;s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic area(s). Provide medical / scientific expert advice / guidance to key customers for assigned product(s) and relevant therapeutic area(s), including scientific exchange and professional relationship development with External Experts (EEs). Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross-functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.</p><p><b>
RESPONSIBILITIES:</b></p><ul><li>
Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.</li><li>
Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.</li><li>
Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).</li><li>
Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.</li><li>
Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.</li><li>
Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)</li><li>
Deliver training to sales forces and other departments; develop and update relevant training materials.</li><li>
Clinical Research Activities:<ul><li>
Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).</li><li>
Provide the required oversight to manage review, approval and conduct of IIS studies.</li><li>
Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).</li></ul></li><li>
Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie&rsquo;s internal policies and guidelines and in accordance with local laws.</li><li>
Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie&rsquo;s policies and procedures and accepted standards of best practice.</li><li>
Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.</li><li>
Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.</li><li>
Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.</li><li>
Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.</li></ul><p></p><p><b><br>
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</b></p><ul><li>
In-Field/Brand Team members (as applicable)</li><li>
Affiliate R&amp;D personnel: Medical Director, Medical operation and Evidence Generation Specialist, Medical Managers/Advisors; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel (as applicable)</li><li>
Marketing and Sales of assigned product and therapeutic area; Market access teams; Affiliate Brand teams.</li><li>
Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC.</li><li>
Area and HQ based Therapeutic Area medical affairs teams.</li><li>
Area Medical Affairs teams</li><li>
Medical Directors and Clinical Teams within Clinical Development Operations and Global Medical Affairs.</li><li>
Healthcare personnel (including physicians, nurses, pharmacists).</li><li>
Participating Research Investigators; thought leaders/external experts.</li><li>
Institutions and Scientific or Medical Societies.</li><li>
Hospitals, other healthcare providers, payers, and Local Regulatory Authorities.</li></ul><p><b>
LOCATION:</b></p><p>
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field.</p><p></p><b><br>
Qualifications</b><br>
<ul><li>
Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered</li><li>
Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.</li><li>
Prior experience in Medical Affairs is required.</li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li><li>
Ability to comprehensively learn about new subject areas and environments.</li><li>
Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.</li><li>
A good understanding of written and oral English is mandatory.</li><li>
Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.</li><li>
Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage.</li><li>
Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate&rsquo;s medical and clinical activities as necessary.</li><li>
Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.</li><li>
High customer orientation and high digital savviness skills.</li><li>
Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>
Ability to travel regularly (approximately 50%)</li></ul><br>
<b>
Additional Information</b><div></div><p><br>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Medical Advisor

Hope Global School

<div><h3 class="jobSectionHeader"><b>Job Description</b></h3>
<div><p>Senior Specialist, Data Governance leads enterprise data governance frameworks, ensuring data quality, compliance, security, and regulatory alignment. This role drives data standards, policies, risk management, and analytics integrity across organizational systems.</p>
</div>
<h3 class="jobSectionHeader"><b>Key Responsibilities</b></h3>
<ul><li>Develop enterprise-wide data governance frameworks and policies</li>
<li>Ensure regulatory compliance across organizational data assets</li>
<li>Monitor data quality metrics and improvement initiatives</li>
<li>Collaborate with stakeholders on data strategy implementation</li>
<li>Define data standards, ownership, and stewardship models</li>
<li>Conduct audits to assess data governance maturity</li>
<li>Manage data risk assessments and mitigation strategies</li>
<li>Oversee metadata management and master data controls.</li>
</ul><h3 class="jobSectionHeader"><b>Skill &amp; Experience</b></h3>
<ul><li>Strong knowledge of data governance frameworks</li>
<li>Expertise in regulatory compliance and data privacy</li>
<li>Advanced analytical and critical thinking abilities</li>
<li>Experience with data management tools platforms</li>
<li>Excellent stakeholder communication and leadership skills</li>
<li>Ability to manage complex enterprise data environments.</li>
</ul>
<p><b>Note:</b> Salary depends on experience and skills and is paid in local currency.</p></div>
<br><div></div><div><ul><li><div><div>Date Posted</div>
<div>February 11, 2026</div>
</div></li><div></div><li><div><div>Location</div>
<div><div>Kuwait City, Kuwait
</div></div></div></li><div></div><li><div><div>Offered Salary:</div>
 <div>18800 - 25500 / year</div>
</div></li><div></div><li><div><div>Expiration date</div>
<div>August 8, 2028
</div></div></li><div></div><li><div><div>Experience</div>
<div>2 Year
</div></div></li><div></div><li><div><div>Gender</div>
<div>Both
</div></div></li><div></div><li><div><div>Qualification</div>
<div>Bachelor Degree</div></div></li></ul></div>

Senior Specialist, Data Governance

Bureau Veritas

<div><div><p>Risk &amp; Safety Engineer</p><p>
ROLES &amp; RESPONSIBILITIES</p><p>
1. Preparation/Review of Environmental and safety assessment studies and other relevant studies.<br>
2. Performs/reports Environmental and Safety studies with minimum quality monitoring<br>
3. Details analysis of environmental and safety studies requirements<br>
4. Selection of most appropriate required study methodology<br>
5. Review of applicable contractual requirements<br>
6. Review and validation of HSE study reports<br>
7. Execution of all required HSE studies<br>
8. Preparation of man-day estimates for proposals and tenders for all studies<br>
9. Meeting with clients to understand the scope of work in the project.<br>
10. Request of data for quoting purposes.<br>
11. Submitting data request forms for collection of data and document reviews for the projects.<br>
12. Attending the Sessions &amp; site visits.<br>
13. Preparation of documents &amp; reports as per the scope of work.<br>
14. Co-coordinating with team in BV Kuwait / any other BV Network for execution of projects.<br>
15. Coordinating with Consultants working for BV Kuwait office as per the requirement.<br>
16. Reviewing reports prepared by consultants before submission to client.<br>
17. Addressing all the comments on each study document &amp; reports received from company / contractors.<br>
18. Maintaining project schedules and deadlines by follow-up.<br>
19. Co-coordinating with HSE Manager &amp; other BV Kuwait staff for all the works.<br>
20. Doing all the works assigned by HSE Manager.<br>
21. Updating technical capability by reading respective journals, presentations and standards.<br>
22. To comply with all the QHSSE rules/regulations of BV as well as Client.</p><p>
AUTHORITIES</p><p>
1. Authority for Stop Work if the situation is Unsafe</p><p>
DESIRED QUALIFICATION &amp; EXPERIENCE</p><p>
1. Graduate Engineer with Minimum 5 + years of Experience or Post Graduate Engineer with 3+ years of Experience or Ph.D. with 1+ years of Experience in HSE</p><p>
2. Experience in execution of various Safety Studies line HAZOP, HAZID, QRA, SIL &amp; PHSER etc.<br>
3. If for Risk &amp; Safety : Experience in Risk Assessment/Process Safety Software is required<br>
4. If for Environmental : Environmental Modeling Software experience is required<br>
5. If for Health : Exposure in Health Assessment is required<br>
6. PHAST, PHAST Risk, PHA Pro, SIL Exsilentia and other equivalent softwares if any (HSE)<br>
7. Fully conversant with HSE Studies/Methods and able to select most appropriate technique</p><p><br>
DESIRED SKILLS</p><p>
1. Excellent Communication Skills.<br>
2. Good basic computer skills<br>
3. Good written &amp; spoken English</p></div></div>

Jr. Engineer - Risk & Safety

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