Join the LLR family of private equity-backed growth companies.

We’re Looking for Experienced Professionals to Join Our Team!

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.

What Makes Suvoda a Great Place to Work?

Here are just a few highlights:

• Your colleagues: You’ll be surrounded by smart, friendly team players that truly care about the work they do, and there are plenty of happy hours and events to connect outside work
• The flexibility: Suvoda creates the perfect environment for people to integrate their work and life, by offering flexible working hours
• The growth and innovation: As part of a growing team, you’ll have lots of opportunities for career development and be exposed to the latest technologies due to our focus on innovation
• The office: Our renovated, modern office space is located in the city center and is equipped with comfortable work spaces, collaborative gathering areas and modern technology that easily connects you to all of our global offices
• The benefits: You’ll have access to a robust benefits package, meal tickets, a top subscription from Romania’s top healthcare provider, a fitness stipend, and competitive salaries with bonus plans
• The industry: By working in clinical trials, you’’ll be part of a challenging and rewarding industry that will allow you to develop your skills quickly while doing your part to change the world!

Responsibilities:

• Ensure activities and deliverables are performed during the software development process as required by Suvoda procedures with no supervision or support.
• Release Suvoda products and systems through the various phases of development.
• Review and approve SDLC and validation deliverables.
• Identify issues during the development of a Suvoda product (or delivery of a Suvoda service) before it is released and ensure that they are reported as per effective procedures.
• Work with delivery teams to perform corrective actions, when necessary.
• Participate in the planning and execution of internal IT validation projects, including external party software validation and migration projects.
• Perform in-process verifications in accordance with Suvoda procedures.
• Identify and lead process improvements, if and when needed.
• Act as a Subject Matter Expert (SME) in areas where expertise has been established, if and when required.
• Develop and deliver C&Q related training supporting materials and holds training sessions, if and when necessary.
• Act as an advisor within the QC function.
• Review deviations from Suvoda’s procedures with supervision and/or support from members of the Quality Control team.

Requirements:

• Bachelor’s degree
• Knowledge of GxP regulations, such as 21 CFR Part 312, Part 11, Annex 11 and ICH E6
• High-achieving personality
• Desire to learn and grow
• Strong work ethic
• Sense of ownership
• Proactive attitude
• Time management and organization skills
• Attention to detail
• Risk-based judgment
• Good communication and technical writing capabilities
• Leadership skills
• Knowledge of Process Improvement techniques

Experience:

• 3 - 5+ years of experience - preferred.