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cra i – min. 6 months monitoring | fluent english Jobs in Istanbul

cra i – min. 6 months monitoring | fluent english

part time english teacher Jobs in Istanbul

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cra i min 6 months monitoring fluent english

Syneos Health

<div>Description
CRA I &ndash; Min. 6 Months Monitoring | Fluent English
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms</li><li>
Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates</li><li>
Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials</li><li>
Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues</li><li>
Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans</li><li>
Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct</li></ul>
Qualifications:<ul><li>
Bachelor's degree in a related field or equivalent experience</li><li>
Minimum of 6 months of experience in clinical research monitoring</li><li>
Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li><li>
Excellent communication and interpersonal skills</li><li>
Ability to work independently and manage multiple priorities</li><li>
Proficiency in using clinical trial management systems and other relevant software</li></ul>
Certifications:<ul><li>
Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li></ul>
Necessary Skills:<ul><li>
Attention to detail and strong analytical skills</li><li>
Problem-solving abilities and critical thinking</li><li>
Ability to work effectively in a team environment</li><li>
Strong organizational and time management skills</li><li>
Proficiency in Microsoft Office Suite</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Minimum of 6 months of experience in clinical research monitoring is requiredFluency in English is requiredRoles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education.Impact and ContributionRoles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes.Core Focus&bull;Conduct thorough on-site and remote monitoring of clinical research studies&bull;Develop and implement tools, procedures, and processes to ensure quality monitoring&bull;Manage defined components of projects or processes within their area of responsibility&bull;Utilize practical knowledge of a professional area, typically obtained through education combined with experience&bull;Maintain high standards of clinical practice and ensure the success of clinical trials</div>

CRA I – Min. 6 Months Monitoring | Fluent English

AstraZeneca

<div>
 At AstraZeneca, we unlock the power of what science can do. Empowered to explore, everyday we work towards our ultimate aim &ndash; treating, preventing, modifying and even curing complex diseases. With an unwavering belief in following the science, we unleash our curiosity. Investing in key areas, harnessing innovative technologies and taking smart risks. Help to shape the future of healthcare as we take our pipeline from strength to strength. Embrace an environment built on lifelong learning. Never complacent, we seek opportunities to expand our knowledge. The place to build a long-term meaningful career. Here we get to develop and grow &ndash; whether that&rsquo;s working at the leading-edge or on varied stages and molecules. Working on things that have never been done before. In return, when great science comes alive, we have the opportunity to get published. We stand together behind a shared ambition. United by our collective passion for having a positive impact on patients&rsquo; lives. Important work that is both meaningful and fulfilling. With the potential to reach over a billion patients across the globe who are living with these complex diseases.
 
 
 
 Background &amp; Qualifications
 
 
 
 <ul>
 <li>
 University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties),
 </li>
 <li>
 Good level of English,
 </li>
 <li>
 Minimum 1 year of experience in a CRA and/or study coordinator positions
 </li>
 <li>
 Strong communication and negotiation skills,
 </li>
 <li>
 Ability to prioritize and handle multiple tasks,
 </li>
 <li>
 Effective planning and organizational skills with a result-oriented approach,
 </li>
 <li>
 Analytical thinking, critical reasoning ability,
 </li>
 <li>
 Good command of MS Office applications,
 </li>
 <li>
 No restriction to travel,
 </li>
 <li>
 Driving License,
 </li>
 <li>
 No military obligation for male candidates.
 
 
 </li>
 </ul>
 
 Job Description
 
 
 
 <ul>
 <li>
 Perform monitoring and site management activities for phase trials projects to assess the progress of clinical projects at assigned investigative/physician sites
 </li>
 <li>
 Ensure clinical project is conducted, recorded, and reported in accordance with the protocol, Company SOPs, ICH-GCP, and all applicable local and legal requirements.
 </li>
 <li>
 May assume clinical functional leadership tasks are assigned, actions as Lead CRA for project
 </li>
 <li>
 Train, support and advise Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
 </li>
 <li>
 Drive performance at the sites. Proactively identify and ensure timely resolution to study-related issues and escalate them as appropriate.
 </li>
 <li>
 Perform regular Site Quality Risk Assessments and adapt monitoring intensity accordingly during the study.
 </li>
 <li>
 Ensure data query resolution in a timely manner.
 </li>
 <li>
 Work with data management to ensure the robust quality of the collected study data.
 </li>
 <li>
 Collaborate with local MSLs as directed by LSM or line manager.
 
 
 </li>
 </ul>
 
 Why AstraZeneca?
 
 
 
 A high performing team, we work hard to not just meet but go beyond the needs of patients and the wider healthcare industry We leverage our partnerships with external experts across the industry, to create and communicate evidence that changes medical practice. As a partner for many, we effectively communicate complex ideas whilst seeking to understand ever-changing needs and requirements. Our valuable contribution and scientific expertise is responsible for advancing our pipeline and accelerating our pathway to finding a cure. Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.
 
 
 
 Where can I find out more?
 
 
 
 Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/
 
 
 Follow AstraZeneca on Instagram https://www.instagram.com/astrazenecaturkiyekariyer/
 
 
 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
</div>

Clinical Research Associate (Biopharma)

<div>Description
CRA II - FSP - Cardiovascular or Nephrology
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms</li><li>
Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates</li><li>
Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials</li><li>
Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues</li><li>
Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans</li><li>
Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct</li></ul>
Qualifications:<ul><li>
Bachelor's degree in a related field or equivalent experience</li><li>
Minimum of 2-4 years of experience in clinical research monitoring</li><li>
Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li><li>
Excellent communication and interpersonal skills</li><li>
Ability to work independently and manage multiple priorities</li><li>
Proficiency in using clinical trial management systems and other relevant software</li></ul>
Certifications:<ul><li>
Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li></ul>
Necessary Skills:<ul><li>
Attention to detail and strong analytical skills</li><li>
Problem-solving abilities and critical thinking</li><li>
Ability to work effectively in a team environment</li><li>
Strong organizational and time management skills</li><li>
Proficiency in Microsoft Office Suite</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education.Impact and ContributionRoles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes.Core Focus&bull;Conduct thorough on-site and remote monitoring of clinical research studies&bull;Develop and implement tools, procedures, and processes to ensure quality monitoring&bull;Manage defined components of projects or processes within their area of responsibility&bull;Utilize practical knowledge of a professional area, typically obtained through education combined with experience&bull;Maintain high standards of clinical practice and ensure the success of clinical trials</div>

CRA II - FSP - Cardiovascular or Nephrology

<div>
 
 
 Qualifications:
 
 
 
 
 
 <ul>
 <li>
 Min. 3 years of experience in procurement or supply chain,
 </li>
 <li>
 Graduation from reputable universities such as Economics, Business Administration, Mathematics, Statistics preferably from Engineering,
 </li>
 <li>
 Fluent level of English,
 </li>
 <li>
 Analytical and proactive personality,
 </li>
 <li>
 Able to meet internal customers&rsquo; expectation,
 </li>
 <li>
 Good at negotiation and communication skills,
 </li>
 <li>
 Able to manage projects
 </li>
 <li>
 Military service must be completed for male candidates,
 </li>
 <li>
 Eligible to act as a team and compatible to team work,
 </li>
 <li>
 Candidates residing in Istanbul Asia are preferred.
 </li>
 </ul>
 
 
 
 
 
 Job Description:
 
 
 
 
 
 <ul>
 <li>
 Manage product families, its categories and sub-categories,
 </li>
 <li>
 Set annual procurement strategies and action plans in line with the organization&rsquo;s products and service needs,
 </li>
 <li>
 Perform marketing analysis to find out new suppliers,
 </li>
 <li>
 Perform supplier management and risk/performance measurements,
 </li>
 <li>
 Manage tender, assessment and negotiation processes with internal customers and suppliers,
 </li>
 <li>
 Manage contract processes,
 </li>
 <li>
 Generate savings in procurement actions
 </li>
 </ul>
</div>

Procurement Assistant Manager / Manager

NielsenIQ

<div>Job Description 
RESPONSIBILITIES:<ul><li>
Contribute to the growth of the Strategic Analytics &amp; Insights (SA&amp;I) with the focus on Consumer &amp; Marketing Insights business, by delivering assigned sales targets.</li><li>
Develop client relationships with previous/ existing clients and new clients through the creation of a positive climate and demonstration of relevance for the client&rsquo;s business.</li><li>
Identify client needs, diagnose client issues and agree on solutions that fully support clients&rsquo; objectives and deliver high growth for our (SA&amp;I) business, liaising with client management personnel to ensure alignment.</li><li>
Drive value from new Strategic Analytics and Insights (SA&amp;I) models/ products by selling these to clients.</li><li>
Promote and market a specific service(s) within the SA&amp;I portfolio internally and externally through presentations, attending meetings, and similar events; contribute to knowledge management about clients locally.</li><li>
Actively identify business opportunities and expand SA&amp;I services to new clients.</li><li>
Be proactive in questioning clients on business issues, use active listening to understand the question behind the question &amp; identify new business opportunities.</li><li>
Prepare proposals and proactively follow up with the client on proposals, designs, costs and drive conversion.</li><li>
Forecast and monitor the revenue vs. target.</li></ul> 
REQUIREMENTS:<ul><li>
University degree</li><li>
Minimum 6 years of experience in Market Research</li><li>
Focused on helping the client win in the market</li><li>
Experience in client management and business development (brief discussions, proposal preparations)</li><li>
Good client service skills and able to communicate</li><li>
Good organizational skills</li><li>
Very good interpersonal skills</li><li>
Fluent in English and Turkish</li><li>
Advanced in Excel and PowerPoint</li></ul> 
#LI-PF1 
 
#LI-Hybrid 
Additional Information<div></div> 
Our Benefits<ul><li>
Flexible working environment</li><li>
Volunteer time off</li><li>
LinkedIn Learning</li><li>
Employee-Assistance-Program (EAP)</li></ul>

About NIQ
NIQ is the world&rsquo;s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights&mdash;delivered with advanced analytics through state-of-the-art platforms&mdash;NIQ delivers the Full View&trade;. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world&rsquo;s population.
For more information, visit NIQ.com
Want to keep up with our latest updates?
Follow us on: LinkedIn | Instagram | Twitter | Facebook

Our commitment to Diversity, Equity, and Inclusion
NIQ is committed to reflecting the diversity of the clients, communities, and markets we measure within our own workforce. We exist to count everyone and are on a mission to systematically embed inclusion and diversity into all aspects of our workforce, measurement, and products. We enthusiastically invite candidates who share that mission to join us. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, marital status, protected veteran status or any other protected class. Our global non-discrimination policy covers these protected classes in every market in which we do business worldwide. Learn more about how we are driving diversity and inclusion in everything we do by visiting the NIQ News Center: https://nielseniq.com/global/en/news-center/diversity-inclusion</div>

Sales Business Partner

Uklon

Uklon is a product-based service IT company and the developer of the eponymous online ride-hailing service. Since April 2025, 97% of the company&rsquo;s corporate rights have been owned by Kyivstar, the largest electronic communications operator in Ukraine. Kyivstar is part of the international VEON Group, a digital operator serving over 160 million customers.VEON provides services in telecommunications, ride-hailing, streaming, medtech, fintech, and other sectors. VEON shares are listed on the NASDAQ stock exchange.Let&rsquo;s drive the industry together!Join us as General Manager in UzbekistanHiring processIntroduction, test assignment and a final meetingIn case you have any questions, feel free to contact our recruiter via email at yelizaveta.belelia@uklon.com.ua - we&rsquo;re here to help!What our offer includes specifically for this role<ul><li>opportunity to grow your career with an international IT company that has Ukrainians roots</li><li>lead and develop Uzbek market with full P&amp;L ownership</li><li>increase business results of the company that unites hundreds of thousands of active customers</li><li>implement your skill set in fostering leadership in the ride-hailing service industry</li><li>a culture of data-driven decision-making</li><li>immersing in a company culture that finds each employee significant and valuable and those, who can influence processes</li><li>bonus component based on achieving goals in the first 6 months</li><li>&#1089;omprehensive relocation package to make your move and start with Uklon as smooth and comfortable as possible</li></ul>How exactly you can influence the developmentof the Company:&#9679;&ensp;create the country's long-term strategy based on local needs, opportunities, and regulations &#9679;&ensp;lead and grow a team of 70+ people &#9679;&ensp;take full ownership of P&amp;L and business objectives &#9679;&ensp;oversee and find cost-effective ways to improve the budget spending &#9679;&ensp;develop a strategy to attract car fleets and private drivers, adapting it based on local specifics and insights &#9679;&ensp;find cost-effective ways to boost our drivers base and loyalty &#9679;&ensp;delve into the details, conduct in-depth analyses, and solve problems &#9679;&ensp;grow the Uklon brand - represent us in the local community and media &#9679;&ensp;advise and closely collaborate with HQ teams such as Product, Legal, or Marketing to develop and execute key initiativesChallenges for six months:&#9679;&ensp;in-depth knowledge and integration into the business: test the service as a Driver for 3-4 days, visit and establish connections with partners and regulators, meet with key team members, and familiarize with all necessary documentation &#9679;&ensp;build and maintain relationships with key partners and secure at least two new partnership &#9679;&ensp;propose 3-4 new solutions that will enhance outcomes and improve team performance &#9679;&ensp;deep understanding of P&amp;L and identification of at least two potential areas for enhancement &#9679;&ensp;develop a comprehensive development strategy for the next 12-24 months &#9679;&ensp;maintain business continuity, achieve key operational targets, such as orders completed and contribution margin &#9679;&ensp;analyze the current organizational structure and propose improvements that will enhance the team's effectivenessTo achieve the results, you will need: &#9679;&ensp;at least 3 years of management experience in fast-moving environments, such as active growth startups, technology, and consulting firms etc &#9679;&ensp;successful experience running operations, bizdev deals &#9679;&ensp;experience in leading a cross-functional team of over 50 individuals, including hiring and participating in organizational restructuring &#9679;&ensp;a business-oriented attitude, goal-oriented &#9679;&ensp;analytical mindset for data-driven decision-making (data-driven/informed approaches) &#9679;&ensp;a jack of many trades who feels comfortable doing anything from hiring to support to product discussions; &#9679;&ensp;easily network with people of all backgrounds &#9679;&ensp;proven experience in leading negotiations for multi-million dollar contracts and the ability to build relationships with C-level executives &#9679;&ensp;experience in management PnL and control of budgeting processes across various departments and core functions of the company &#9679;&ensp;fluent in English, Russian, Uzbek is a plusHow do you manage your working hours? &#9679;&ensp;8-hour working day, from 9 a.m. to 6 p.m., Monday to Friday &#9679;&ensp;cooperation in accordance with the legislation of UzbekistanHow will you level up your skills in Uklon? Education and development: &#9679;&ensp;Corporate library &#9679;&ensp;Long-term training of managers &#9679;&ensp;Internal knowledge sharing &#9679;&ensp;Subscription to thematic resources &#9679;&ensp;Corporate English lessons &#9679;&ensp;Annual team budgets for training &#9679;&ensp;Referral programCare and support: &#9679;&ensp;Support for maternity and paternity leave &#9679;&ensp;Paid sick leave &#9679;&ensp;Sport activities &#9679;&ensp;Corporate team buildings &#9679;&ensp;Presents for holidays &#9679;&ensp;Financial support with the loss of a relative.Join Uklon!Job Type: Full-timeApplication Question(s):<ul><li>Your location now</li><li>Are you ready to relocate to Tashkent?</li></ul>Language:<ul><li> English (Required)</li><li>Russian (Required)</li><li>Uzbek (Required)</li></ul>

General Manager in Tashkent (Relocation package)

HSH Group (owner and operator of The Peninsula Hotels)

<div><div>Set along the dazzling Bosphorus waterfront in the historic district of Karak&ouml;y, The Peninsula Istanbul provides a showcase for both vibrant Turkish culture and superlative hospitality within Galataport, a new waterfront revitalisation project. The hotel is comprised of four exquisite buildings &ndash; three of them historic and beautifully restored &ndash; and welcomes guests arriving by land or sea.</div> 
<div></div>
<ul>
<li>An exceptional opportunity to join our high-profile hotel in Istanbul.</li>
<li>The Peninsula Hotels espouses luxury service, dedication to our customers, and commitment to our employees.</li>
<li>Be a part of the highly experienced team.</li></ul> 
<div></div>
<div>
Key accountabilities</div> 
<div></div>
<ul>
<li>Handles all guest and internal customer complaints and inquiries in a courteous and efficient manner, following through to ensure problems are resolved satisfactorily.</li>
<li>Patrols lobbies, corridors, guest floors and public areas and makes use of the i-Guard System appropriately, while ensuring there are no fires, unsafe conditions, and/or missing or inoperative safety equipment.</li>
<li>Ensures that the Hotel&rsquo;s policy and procedures in key issuance are adhered to at all times.</li>
<li>Ensures that the Hotel&rsquo;s policy &amp; procedures on the issuance of Security Passes are adhered to for all visitors including suppliers, contractors, part-timers, employees etc.</li>
<li>Ensures that tasks and duties listed for designated posts such as Employee Entrance, Control Room, Patrol, Main Lobby and Hotel Driveway are professionally carried out at all times.</li>
<li>Assists in the tasks assigned during Hotel Fire &amp; Evacuation situations.</li>
<li>Questions any suspicious character in a polite manner; refuses entry if the subject is not able to provide reasonable reply; requests for assistance immediately if the situation arises.</li></ul> 
<div> 
General requirements</div> 
<div></div>
<ul>
<li>Excellent knowledge of security industry best practice across relevant security operations (loss prevention, conflict resolution, access control, etc.).</li>
<li>Knowledge of security and crisis management related law and regulation.</li>
<li>Experience using relevant technology and equipment.</li>
<li>Min. 5 years experience.</li>
<li>5188 Private Security Licence.</li>
<li>Good in English language proficiency.</li></ul><div></div><div> 
We would be delighted to receive your CV and will liaise directly with suitable applicants.</div></div><div></div>

Security Officer

Explore 888+ Cra i min 6 months monitoring fluent english in Istanbul this September. Find roles across top companies and apply now to boost your career.