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Software Developer III (C#, .NET)

Clincierge

Role overview

Qualifications

  • Bachelor’s degree preferred
  • At least 2 years of experience in a similar role
  • Prior working experience in developing web applications with C#, .NET (Framework or Core), SQL Server, MVC and EF
  • High achieving personality

Responsibilities

  • Work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management
  • Review user requirements specifications, verifying that all requirements can be implemented with Suvoda software
  • Assist with the creation of implementation design and technical design documentation
  • Develop software systems that are reliable, maintainable, and efficient, with emphasis on patient safety and data integrity

Key facts

Hard skills

C (Programming Language) .NET C# (Programming Language) .NET Entity Framework Model View Controller Interactive Response Technology Software Development Property Ownership

Other skills

  • Troubleshooting (Problem Solving)
  • Communication
  • Teamwork
  • Time Management
  • Detail Oriented
  • Strong Work Ethic

About the company

Clincierge logo

Clincierge

Contract Research Organizations (CRO)

Improve your clinical trial retention rates while increasing study access and diversity. Clincierge reduces the emotional, logistical, and financial barriers to clinical trial participation, enabling patients to access life-changing and potentially lifesaving new treatment options. Our high-touch patient concierge services include but are not limited to, individualized air and rail ticketing, hotel and housing accommodations, payment and reimbursement processes, and ongoing patient, family, and caregiver support. Our services reduce the emotional and financial stressors related to travel and out-of-pocket expenses related to clinical trial participation. We address unique patient and caregiver needs, and the many demands complex trial designs place on participants and their families, building custom solutions to specific study-related problems. Our multilingual, in-country Clincierge Coordinators provide seamless logistical support for patients, their families, and caregivers. From initial patient enrollment in a Clincierge-supported study to trial completion, they offer much-needed emotional support and personalized communications each step of the way. This concierge level of patient support assists trial sponsors, CROs, and research institutions in managing the cost and duration of their clinical trials. Clincierge’s value-added services not only enhance patient recruitment and improve retention, but they also relieve clinical research associates, clinical investigators, and other study sponsors and trial site personnel from time-consuming patient logistics. Our services enable study staff to prioritize patient care and focus on study outcomes. We reduce clinical trial administrative costs and streamline patient payments and reimbursements through our efficient online portal.

Company details

Company typeScaleup
IndustryContract Research Organizations (CRO)
Company size51 - 200

Links

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Job description

Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.

Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.

 

Responsibilities: 

  • Work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management
  • Review user requirements specifications, verifying that all requirements can be implemented with the Suvoda software in the required timeframe
  • Assist with the creation of implementation design and technical design documentation
  • Develop software systems that are reliable, maintainable, and efficient, with emphasis on patient safety and integrity of clinical study data
  • Manage the deployment of Suvoda IRT systems into all environments, completing all required documentation
  • Assist the support team with troubleshooting and resolution of issues reported on production systems
  • Participate in the product research and development process by providing the engineering team with new solutions and ideas based on project experience
  • Generate ideas for innovative technological solutions to increase the quality of Suvoda system
  • Perform other related duties as required

 

Requirements:

  • Bachelor’s degree prefered
  • At least 2 years of experience in a similar role
  • Prior working experience in developing web applications with C#, .NET (Framework or Core), SQL Server, Model View Controller (MVC) and Entity Framework (EF)
  • High achieving personality
  • Desire to learn and grow
  • Strong work ethic
  • Sense of ownership
  • Proactive attitude
  • Time management and organizational skills
  • Attention to detail

 

#LIAA1

We are aware that an individual(s) are fraudulently representing themselves as Suvoda recruiters and/or hiring managers. Suvoda will never request personal information such as your bank account number, credit card number, drivers license or social security number — or request payment from you — during the job application or interview process. Any emails from the Suvoda recruiting team will come from a @suvoda.com email address. You can learn more about these types of fraud by referring to this FTC consumer alert. 

As set forth in Suvoda’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

If you are based in California, we encourage you to read this important information for California residents linked here.

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Marcus Rivera

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