As an Accounts Receivable Coordinator I at Syneos Health, you will play a crucial role in the invoicing and cash application process. Your responsibilities will include: - Prepare invoice packages by extracting data from consolidated monthly files, creating pivot tables, and compiling scanned image backup. - Route prepared invoice packages to Project Managers for review and approval. - Generate pass-through invoices in Oracle and create invoice PDF packages for clients. - Update the Billing Repository with invoice details and respond to invoice-related queries from operations or clients. - Generate investigator invoices in Oracle, provide details of corrections to the Billing supervisor, and process credits and rebills as required. Qualifications required for this role include: - 1-3 years of experience in invoicing and cash application. - Knowledge of invoice generation, credit memo processing, and working with ERP systems like Oracle. - Strong written and verbal communication skills, along with intermediate to advanced Excel skills. - Experience in a multi-currency environment and good organizational skills. - Ability to communicate effectively with colleagues and clients in different countries, with attention to detail and accuracy. Desirable qualifications include experience using the Oracle ERP system. In addition to the above responsibilities and qualifications, Syneos Health is dedicated to developing its employees through career progression, training programs, and a supportive work culture. The company prides itself on creating a diverse and inclusive environment where everyone can contribute their unique perspectives. Syneos Health has a proven track record of working with a wide range of pharmaceutical products and studies globally. Join us in challenging the status quo and making a difference in the biopharmaceutical industry. For more information about Syneos Health, visit http://www.syneoshealth.com. As an Accounts Receivable Coordinator I at Syneos Health, you will play a crucial role in the invoicing and cash application process. Your responsibilities will include: - Prepare invoice packages by extracting data from consolidated monthly files, creating pivot tables, and compiling scanned image backup. - Route prepared invoice packages to Project Managers for review and approval. - Generate pass-through invoices in Oracle and create invoice PDF packages for clients. - Update the Billing Repository with invoice details and respond to invoice-related queries from operations or clients. - Generate investigator invoices in Oracle, provide details of corrections to the Billing supervisor, and process credits and rebills as required. Qualifications required for this role include: - 1-3 years of experience in invoicing and cash application. - Knowledge of invoice generation, credit memo processing, and working with ERP systems like Oracle. - Strong written and verbal communication skills, along with intermediate to advanced Excel skills. - Experience in a multi-currency environment and good organizational skills. - Ability to communicate effectively with colleagues and clients in different countries, with attention to detail and accuracy. Desirable qualifications include experience using the Oracle ERP system. In addition to the above responsibilities and qualifications, Syneos Health is dedicated to developing its employees through career progression, training programs, and a supportive work culture. The company prides itself on creating a diverse and inclusive environment where everyone can contribute their unique perspectives. Syneos Health has a proven track record of working with a wide range of pharmaceutical products and studies globally. Join us in challenging the status quo and making a difference in the biopharmaceutical industry. For more information about Syneos Health, visit http://www.syneoshealth.com.
As a Node.js Developer at our company, you will be responsible for developing, maintaining, and optimizing backend services using Node.js. Your key responsibilities will include: - Developing, maintaining, and optimizing backend services using Node.js. - Building and integrating RESTful APIs and/or GraphQL APIs. - Working with databases such as MongoDB, MySQL, or PostgreSQL. - Writing clean, reusable, and efficient code following best practices. - Implementing authentication and authorization using JWT/OAuth. - Integrating third-party APIs and services. - Collaborating with front-end developers to integrate APIs with UI applications. - Troubleshooting, debugging, and resolving performance issues. - Participating in code reviews and contributing to architecture discussions. - Working in Agile/Scrum teams and participating in sprint planning. - Ensuring application security, scalability, and reliability. In addition to the key responsibilities, the ideal candidate for this role should have the following qualifications: - Strong proficiency in Node.js and JavaScript (TypeScript preferred). - Experience with frameworks like Express.js, NestJS, or Fastify. - Hands-on experience with MongoDB / MySQL / PostgreSQL. - Familiarity with NoSQL and SQL database concepts. - Knowledge of asynchronous programming, promises, and async/await. - Experience with Git and version control. - Good understanding of API design, middleware, and microservices concepts. - Experience with package managers like npm or yarn. If you are looking for a Full-time Node.js Developer position and have at least 1 year of experience with Node.js, we encourage you to apply. The work location is in Hyderabad, Telangana. Relocation to Hyderabad is preferred for this role. As a Node.js Developer at our company, you will be responsible for developing, maintaining, and optimizing backend services using Node.js. Your key responsibilities will include: - Developing, maintaining, and optimizing backend services using Node.js. - Building and integrating RESTful APIs and/or GraphQL APIs. - Working with databases such as MongoDB, MySQL, or PostgreSQL. - Writing clean, reusable, and efficient code following best practices. - Implementing authentication and authorization using JWT/OAuth. - Integrating third-party APIs and services. - Collaborating with front-end developers to integrate APIs with UI applications. - Troubleshooting, debugging, and resolving performance issues. - Participating in code reviews and contributing to architecture discussions. - Working in Agile/Scrum teams and participating in sprint planning. - Ensuring application security, scalability, and reliability. In addition to the key responsibilities, the ideal candidate for this role should have the following qualifications: - Strong proficiency in Node.js and JavaScript (TypeScript preferred). - Experience with frameworks like Express.js, NestJS, or Fastify. - Hands-on experience with MongoDB / MySQL / PostgreSQL. - Familiarity with NoSQL and SQL database concepts. - Knowledge of asynchronous programming, promises, and async/await. - Experience with Git and version control. - Good understanding of API design, middleware, and microservices concepts. - Experience with package managers like npm or yarn. If you are looking for a Full-time Node.js Developer position and have at least 1 year of experience with Node.js, we encourage you to apply. The work location is in Hyderabad, Telangana. Relocation to Hyderabad is preferred for this role.
You are a Consulting Analyst who will support clients in the life sciences and healthcare industries in solving complex business challenges. Your responsibilities will include: - Conducting secondary research and data analysis to inform strategic recommendations and client deliverables. - Supporting cross-functional project management both internally and at client organizations. - Helping clients navigate transformation driven by changes in strategy, operating models, processes, or technology. - Identifying relevant data sources and applying critical thinking to generate creative, evidence-based solutions. - Assisting in the development of compelling, structured, and logical storyboards and presentations. - Contributing to commercialization strategies, including launch planning, customer engagement, and market positioning. - Communicating findings effectively using text, graphics, and other visual formats. - Maintaining professionalism and adaptability in response to project ambiguity, client changes, and unexpected data findings. - Building and maintaining strong working relationships with clients, team members, and internal stakeholders. - Participating in proposal development and business development efforts. - Engaging in internal initiatives, training sessions, and professional development activities. - Supporting continuous improvement of internal processes, methodologies, and service offerings. Qualifications Required: - Bachelors degree - Strong analytical skills and the ability to think critically and creatively on engagements - Strong business acumen and demonstrated attention to detail - Strong presentation skills Desired Qualifications: - Post Graduation in business or life sciences - Work experience in the consulting, pharmaceutical or biotech industries - Life sciences R&D operational experience - Ability to travel - Understanding of the end-to-end pharmaceutical/biotech value chain At Syneos Health, you will be a part of a diverse, inclusive, and authentic workplace that values your unique skills and perspectives. Join a global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients and changing lives around the world. You are a Consulting Analyst who will support clients in the life sciences and healthcare industries in solving complex business challenges. Your responsibilities will include: - Conducting secondary research and data analysis to inform strategic recommendations and client deliverables. - Supporting cross-functional project management both internally and at client organizations. - Helping clients navigate transformation driven by changes in strategy, operating models, processes, or technology. - Identifying relevant data sources and applying critical thinking to generate creative, evidence-based solutions. - Assisting in the development of compelling, structured, and logical storyboards and presentations. - Contributing to commercialization strategies, including launch planning, customer engagement, and market positioning. - Communicating findings effectively using text, graphics, and other visual formats. - Maintaining professionalism and adaptability in response to project ambiguity, client changes, and unexpected data findings. - Building and maintaining strong working relationships with clients, team members, and internal stakeholders. - Participating in proposal development and business development efforts. - Engaging in internal initiatives, training sessions, and professional development activities. - Supporting continuous improvement of internal processes, methodologies, and service offerings. Qualifications Required: - Bachelors degree - Strong analytical skills and the ability to think critically and creatively on engagements - Strong business acumen and demonstrated attention to detail - Strong presentation skills Desired Qualifications: - Post Graduation in business or life sciences - Work experience in the consulting, pharmaceutical or biotech industries - Life sciences R&D operational experience - Ability to travel - Understanding of the end-to-end pharmaceutical/biotech value chain At Syneos Health, you will be a part of a diverse, inclusive, and authentic workplace that values your unique skills and perspectives. Join a global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients and changing lives around the world.
As a Senior Clinical Programmer at Syneos Health, you will utilize primary development tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software to meet specifications efficiently. Your responsibilities will include: - Generating and maintaining all necessary documentation for clinical programming projects, including specifications, programs, and validation efforts. - Serving on project teams to coordinate and lead development activities, attending meetings, and providing constructive feedback. - Providing technology support to clinical programming staff and project analysts, ensuring timely and productive software development. - Ensuring high-quality deliverables by providing senior review of study level/program level/multi-study core deliveries for accuracy. - Monitoring applications for workflow alerts, system errors, and performance issues, and providing second-tier help desk support when needed. Additionally, you will be expected to have the following qualifications: - Bachelor's degree preferred, or equivalent combination of related education and experience. - Minimum 5+ years of experience in Clinical Programming. - Experience in listings programming, creating Macros, Study build, and SAS Mapping preferred. - Good communication skills and the ability to effectively deal with sponsors and internal customers. - Preferred Base and Advanced SAS certification. - Proficiency in Microsoft Office Suite and experience with programming languages such as PL/SQL, SAS, C#, or VB preferred. Syneos Health is committed to developing its employees and creating a supportive and engaging work environment where diversity is celebrated. By joining us, you will have the opportunity to work on cutting-edge projects that aim to change lives and make a meaningful impact in the biopharmaceutical industry. Please note that the tasks, duties, and responsibilities outlined in this job description are not exhaustive, and the Company may assign additional responsibilities at its discretion. The Company values equivalent experience, skills, and education, and will consider candidates based on these qualifications. Learn more about Syneos Health at http://www.syneoshealth.com. As a Senior Clinical Programmer at Syneos Health, you will utilize primary development tools such as Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS to design, write, validate, and maintain software to meet specifications efficiently. Your responsibilities will include: - Generating and maintaining all necessary documentation for clinical programming projects, including specifications, programs, and validation efforts. - Serving on project teams to coordinate and lead development activities, attending meetings, and providing constructive feedback. - Providing technology support to clinical programming staff and project analysts, ensuring timely and productive software development. - Ensuring high-quality deliverables by providing senior review of study level/program level/multi-study core deliveries for accuracy. - Monitoring applications for workflow alerts, system errors, and performance issues, and providing second-tier help desk support when needed. Additionally, you will be expected to have the following qualifications: - Bachelor's degree preferred, or equivalent combination of related education and experience. - Minimum 5+ years of experience in Clinical Programming. - Experience in listings programming, creating Macros, Study build, and SAS Mapping preferred. - Good communication skills and the ability to effectively deal with sponsors and internal customers. - Preferred Base and Advanced SAS certification. - Proficiency in Microsoft Office Suite and experience with programming languages such as PL/SQL, SAS, C#, or VB preferred. Syneos Health is committed to developing its employees and creating a supportive and engaging work environment where diversity is celebrated. By joining us, you will have the opportunity to work on cutting-edge projects that aim to change lives and make a meaningful impact in the biopharmaceutical industry. Please note that the tasks, duties, and responsibilities outlined in this job description are not exhaustive, and the Company may assign additional responsibilities at its discretion. The Company values equivalent experience, skills, and education, and will consider candidates based on these qualifications. Learn more about Syneos Health at http://www.syneoshealth.com.
As a Statistical Programmer II at Syneos Health, you will play a crucial role in the generation of summary tables, data listings, graphs, and derived datasets using SAS or other software as per the statistical analysis plan and programming specifications. Your responsibilities will include: - Ensuring that outputs meet quality standards and project requirements. - Performing validation programming and collaborating with other Statistical Programmers and Biostatisticians to resolve discrepancies. - Keeping the project team informed of programming progress and addressing any issues requiring attention. - Following applicable SOPs, WIs, and regulatory guidelines such as ICH. - Maintaining well-organized project documentation and verification/quality control documents for inspection readiness. - Managing scheduling and time constraints across multiple projects, setting goals based on management priorities, and adapting to changes in timeline or priorities. - Developing specifications for datasets and outputs according to statistical and Sponsor requirements. - Anticipating and addressing potential programming issues, defining variables accurately for peer review with little rework. - Contributing ideas in internal meetings, respecting opinions of others, and collaborating with team members on various projects and initiatives. - Completing project programming activities within the allotted timeframe and assisting with the transfer of deliverables. - Acting as the Lead Statistical Programmer when required, directing programming activities and monitoring progress on deliverables. - Performing any other work-related duties as assigned with minimal travel requirements. Qualifications for this role include: - An Undergraduate Degree, preferably in a scientific or statistical discipline; or an equivalent combination of education and demonstrated programming experience. - Proficiency in programming in SAS or other required software, particularly in a clinical trial environment. - R programming skills and experience in Anonymization of Clinical Datasets are preferred. - Familiarity with SDTM/ADaM theoretical knowledge and hands-on experience will be beneficial. - Excellent written and verbal communication skills. - Knowledge of the drug development process (Phase I through IV) and general regulatory requirements. - Ability to manage multiple studies, with study lead experience. - Capability to read, write, speak, and understand English fluently. Syneos Health is dedicated to creating a diverse and inclusive work environment where every individual feels valued. With a focus on career development, technical training, and peer recognition, we aim to build a company that is not only great to work with but also great to work for. Join us in our mission to accelerate customer success and change lives through innovative solutions in the biopharmaceutical industry. Discover more about Syneos Health and the impactful work we do at http://www.syneoshealth.com. As a Statistical Programmer II at Syneos Health, you will play a crucial role in the generation of summary tables, data listings, graphs, and derived datasets using SAS or other software as per the statistical analysis plan and programming specifications. Your responsibilities will include: - Ensuring that outputs meet quality standards and project requirements. - Performing validation programming and collaborating with other Statistical Programmers and Biostatisticians to resolve discrepancies. - Keeping the project team informed of programming progress and addressing any issues requiring attention. - Following applicable SOPs, WIs, and regulatory guidelines such as ICH. - Maintaining well-organized project documentation and verification/quality control documents for inspection readiness. - Managing scheduling and time constraints across multiple projects, setting goals based on management priorities, and adapting to changes in timeline or priorities. - Developing specifications for datasets and outputs according to statistical and Sponsor requirements. - Anticipating and addressing potential programming issues, defining variables accurately for peer review with little rework. - Contributing ideas in internal meetings, respecting opinions of others, and collaborating with team members on various projects and initiatives. - Completing project programming activities within the allotted timeframe and assisting with the transfer of deliverables. - Acting as the Lead Statistical Programmer when required, directing programming activities and monitoring progress on deliverables. - Performing any other work-related duties as assigned with minimal travel requirements. Qualifications for this role include: - An Undergraduate Degree, preferably in a scientific or statistical discipline; or an equivalent combination of education and demonstrated programming experience. - Proficiency in programming in SAS or other required software, particularly in a clinical trial environment.