Software Development Engineer at BIOCLINICA INC DBA CLARIS

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

07 Jun, 26

Salary

0.0

Posted On

09 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

.NET/C#, Angular, JavaScript, Python, Object Oriented Programming, Agile SCRUM, RDBMS, Visual Studio, GitLab, TFS, JIRA, English

Industry

Biotechnology Research

Description

We are looking for you as Software Development Engineer II (f/m/d) at our ) for developing and successfully delivering a project-specific highly-interactive web and other software applications for clinical research data acquisition and data management that is deployed onto worldwide distributed Smartphones, Tablets and Asthma monitor devices. Become a part of driving clinical studies forward faster with your daily performance with us. You will be responsible for ensuring that our customers (pharmaceutical companies, BioTechs, and CROs) receive software applications according to the study specifications. Even if you don't have experience in the world of clinical trials, we'd love to show you! What we offer: Flexible working hours and working time accounts to support the work-life balance Support your professional development through internal and external training and certification programs Salary plus Annual bonus target Company pension scheme What you'll be doing: Join our team of international Software Development Engineers! We're excited to welcome a new team member who can support projects and collaborate on technical questions. Work collaboratively within an international team of Software Development Engineers, supporting projects and addressing technical questions. Develop, deploy, and maintain software applications based on clinical trial software specifications. Participate in decision-making throughout the development life cycle Contribute to project specification development and the planning and deployment scheduling process. Review moderate to high-complexity code from other engineers and write your own high-quality code. Communicate timelines, scope, and technical concerns effectively to internal stakeholders. Present technical decisions through presentations, tech talks, and wiki documentation. Collaborate with cross-functional teams, including Design, Quality, Translations, and Project Management, to ensure project success. Negotiate and resolve study team issues related to timelines, schedules, and technical changes. What we look for: Degree in Computer Science or a related field (or equivalent experience). 2+ years of software development experience Good knowledge in object oriented programming Technical expertise in .NET/C#, Angular, and JavaScript. Understanding of Python programming, including core concepts and best practices is a plus Strong ability to prioritize multiple projects in a fast-paced environment with tight timelines. Experience in IDE, Repository, Issue tracking systems (Visual Studio, Eclipse, GitLab, TFS, JIRA) Understanding of Relational Database Management Systems (RDBMS) Experience in SW development methodologies; Agile SCRUM Proficiency in English (spoken and written) At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials. The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. Clario reserves the right to amend or change this job description to meet the needs of Clario. This job description and any attachments do not constitute or represent a contract. The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.

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Responsibilities

The role involves developing, deploying, and maintaining highly-interactive web and software applications for clinical research data acquisition and management across various devices. Responsibilities include collaborating with international teams, reviewing code, contributing to specifications, and communicating technical concerns to stakeholders.