Intego Group — вакансії

Intego Group is looking for a Senior API/Middleware Developer to take part in a project for the US national tires distribu-tion company and its high-volume critical customers. This project requires a person who can understand the functional requirements set forth for a business function that will enable the automation of business procedures. You will drive the architecture for the solution in collaboration with the client’s development leaders.

About our client:

Our client is a national tire distributor that delivers to U.S. tire and automotive retailers the full passenger and light truck tire portfolios of Goodyear and Bridgestone. They’re out to set a new standard of excellence for tire distribution in the U.S., and they’ll do it by focusing on the needs of dealers and their customers.

Role Specifics:

• Responsible for implementing API/Middleware Architectural goals.
• Supports formulating API/Middleware technical roadmap, technical debt.
• Supports standards for API/Middleware security, performance, stability.
• Partially responsible for coordinating and performing API/Middleware maintenance / third level (senior) technical support (shared with Support groups).

General Requirements:

• Expert level knowledge of ASP.NET Core Web API is required.
• At least 3-4 years of hands-on experience with .NET is needed for success.
• Expert level knowledge of .NET fundamentals – Object Oriented Development, Generics, LINQ, Entity Framework, Unit Testing.
• Some SQL Server knowledge is desired (at the level of Transact SQL, no administration skills necessary)
• Some experience with design and prototyping tools and diagramming is desired.
• Decent understanding of microservices architecture and related patterns is desired.
• Expert level understanding of API versioning, management, telemetry, performance tuning and API documentation techniques (swagger or similar).
• Able to create technical debt and technical roadmap assessments for API products.
• Able to peer review, improve and implement presented Solution / Enterprise Architecture artefacts.
• Basic understanding fundamentals of reliable/repeatable processes, monitoring, compensation, graceful degradation is required.

Education and Background:

• Bachelor’s degree in computer science or similar related discipline is preferred, but not absolutely required.
• Hands on experience is prioritized.
• Strong English skills.

Additional traits specific to the position that are desired:

• Ability to remain calm and productive under pressure, in a dynamic, fast paced environment.
• Rapid, value-add oriented decision-making ability.
• Intense customer focus.
• Ability to adapt to change, to direct/control change and to facilitate change.
• Ability to accept and carry responsibility without reservation.
• Ability to perform with minimal supervision, identifying and proactively communicating on all pre-requisites for successful performance.
• Strong communication skills preferred.
• Ability to collaborate with cross-functional business team, identifying additional technical solutions that will enable the client to keep their promise of providing industry-leading service.

We’re looking for bright individuals to join our growing team in the Poland office.
You will be responsible for all aspects of clinical database review, cleaning, reporting, participating in database design and implementation as well as client communication and team oversight. As a Senior Clinical Data Manager, you will establish and maintain policies and procedures for gathering, analyzing, and reporting clinical trial data.

Job responsibilities:

The role of the Clinical Data Manager is to ensure useful, accurate, and reliable information is collected during clinical trials. This involves the careful design of the data collection tools and data interpretation methodology as well as close integration with other clinical study management functions.

General responsibilities include:

• Review clinical trial data in alignment with client SOPs and data review conventions to identify erroneous, missing, incomplete, or implausible data.
• Perform query production, resolution, and tracking to resolve any problematic data identified during the review. Update the database accordingly.
• Create and/or review data management documentation, completion guidelines, DMP, DVS and other specifications.
• Take part in EDC system and CRF components design and testing.
• Interact with clinical, programming, and other project teams, as necessary.
• Communication with the client/sponsor, leading the project.
• Team oversight and tasks planning.

General requirements:

• Bachelor’s Degree, or educational equivalent, in health, clinical, biological, or related discipline, and 3 to 5 or more years of direct data management experience;
• Knowledge of medical terminology, pharmacology, anatomy, and/or physiology;
• Knowledge of operating procedures and work instructions and the ability to apply them in practice;
• Knowledge of GCP and relevant regulatory guidelines;
• Strong English skills. Excellent communication, interpersonal, customer service, and teamwork skills;
• Excellent organizational and analytical skills;
• Comprehensive understanding of the clinical drug development process;
• Experience with electronic Clinical Database Systems is required and experience with electronic reporting applications is preferred;
• Experience with an electronic data capture (EDC);
• Ability to maintain a high degree of confidentiality with clinical data and proprietary data;
• Ability to use interactive computer programs, such as MS Word, Excel, and PowerPoint;
• Extensive data management skills and thorough knowledge of the data management process (e.g., therapeutic area, deep understanding of DM processes, SAE reconciliation/pharmacovigilance, medical review, external data vendor reconciliation, management of central/local laboratory data, and/or new technology).