12 Payment Specialist jobs in India

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at .
We are a global pharmaceutical company dedicated to transforming innovative science into medical solutions that deliver value and hope to patients and their families. By focusing on addressing unmet medical needs and operating with ethics and integrity, we strive to enhance the health and well-being of people worldwide.
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico. The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
**Purpose and Scope:**
+ Responsible for execution of work within the Global Site Payment support function in support of both early and late-stage Clinical Operations.
+ This position supports site payment related activities and will report on performance timelines.
+ This position is accountable for the timely delivery of clinical site payments according to the site contract timelines.
**Essential Job Responsibilities:**
+ Responsible for the effective management of site payments to investigative sites within the Veeva Site Payment system
+ Manage and support the day to day operations of site payment processing per established contractual agreements and objectives in compliance with applicable GCP / ICH guidelines and other JSOX / FAR requirements
+ Provide regular updates of payment status to Clinical Study teams and leadership
+ Data entry support into Veeva Site Payment system or CTMS system
+ Site Payment related activities, as required, including the supplier onboarding activities, mailbox management, invoice review and upload, invoice approval against CTMS and EDC (other source data as required), and invoice confirmation for payment
+ Support investigator payments from invoice receipt through payment including monitoring of status throughout the process to ensure compliance with contract timelines
+ Manage pro-forma invoice payments as needed
+ Support of advance payment and suitability / pre-payments
+ Collaborate with cross functional stakeholders as process requires, including feasibility, study start up, contracts, budget and study team members
+ Work to proactively identify and resolve payment issues that arise throughout the life of the study (study start up, conduct and close out) including support and oversight of site payment escalations
+ Oversee site payment systems, standards and processes to ensure timely payment of the investigative sites (either via our vendors or internal payment via Veeva)
+ Support of input into site payment metrics for functional area, including but not limited to the input, measurement and monitoring.
+ Bachelor's Degree or equivalent relevant experience
+ At least 1 to 3 years prior experience handling and executing on functional specific material (e.g. site payments or related payment or budget related material) matters
+ Understanding of the regulatory, legal and data privacy issues affecting the pharmaceutical industry, including GDPR as it relates to the core and country templates.
+ Strong ability to grasp regulatory and legal issues quickly, exhibit strong analytical problem solving and decision-making skills, exercise sound judgment.
+ Strong communication skills (both oral and written).
+ Must have a knowledge of clinical development processes and ICH/GCP
+ Must have strong interpersonal, written, verbal, and computer skills.
+ Minimal (10%) travel required
+ Fluent in English
**Preferred Qualifications:**
+ Experience working in a Global environment
**Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
Category Site Activation / Late-Stage Management
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way.
We are a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials - from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill.
**Job Purpose and Impact**
The Transaction Management Specialist will execute and administer moderately complex aspects of Trade and Capital Markets activities in a timely and accurate manner. In this role, you will deliver clean, agile, and customer-focused execution of the operational activities while ensuring compliance to the established guidelines and procedures.
**Key Accountabilities**
+ Process standard deals in the trade inventory system and prepare all documents based on approved templates.
+ Coordinate and align with external and internal stakeholders to resolve execution issues, assisting as necessary.
+ Settle standard transactions to ensure quality settlement for supervisor's review.
+ Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff.
+ Support system upgrades and process improvement initiatives to ensure operational excellence and efficiency.
+ Other duties as assigned
**Qualifications**
**Minimum Qualifications**
+ Bachelor's degree in a related field or equivalent experience
+ Minimum of four years of related work experience
+ Fluent in verbal and written English
+ Other minimum qualifications may apply.
**Preferred Qualifications**
+ Experience in trade finance operations
+ Proven ability to interpret and apply transaction-related documentation with precision, ensuring accurate execution and compliance
+ Exposure to process optimization, automation initiatives, or digital tools supporting operational efficiency
+ Ability to work independently while contributing to team goals in a fast-paced, dynamic environment
**Our Offer**
We provide a fast paced stimulating international environment, which will stretch your abilities and channel your talents. We also offer competitive salary and benefits combined with outstanding career development opportunities in one of the largest and most solid private companies in the world.
**Interested? Then make sure to send us your CV and cover letter in English today:**
**Follow us on LinkedIn:** ** is committed to being an inclusive employer. Click here to find out more