We Are Hiring: Project Manager

November 10, 2025

We Are Hiring: Project Manager

Flex Databases team is looking for a Project Manager to join our Customer Success Management team, based in our Prague office. While this role can be fully remote within Czechia, you must be available to visit the office for occasional client meetings. 

Preferred location: Prague. 

Fluency in German is essential for this position, as you will be working closely with our German-speaking clients and must be able to communicate with them effectively in German. 

We create flexible e-Clinical software for Contract Research Organizations (CROs) and pharmaceutical companies, empowering professionals worldwide to conduct research and develop effective medicines. 

As a remote-first company with a global client base, we embrace flexibility while maintaining some physical presence in our offices in the Czech Republic, Switzerland, Turkey, and the US. 

What you’ll do: 

As our new colleague, you will join us in building our customers’ loyalty and developing our product by: 

  • Serve as the key contact for customer engagement throughout various stages of our relationships, including implementation, onboarding, and ongoing support. 
  • Successfully implement the system for clients within the timeline and budget and promote its ongoing usage. 
  • Act as a product expert to understand customer use cases and business processes, providing relevant guidance and value through demos, training, and support materials. 
  • Collaborate with internal product and technical teams to translate customer insights into product development and roadmap ideas. 
  • Focus on churn prevention by consistently collecting feedback and analyzing product usage and trends. 
  • Grow existing accounts by identifying upsell opportunities and partnering with Sales and Product teams to drive revenue growth 
  • Build and maintain long-term customer relationships while ensuring high satisfaction and increasing LiveTime Value. 
  • Define project scope, goals, timelines, and deliverables, plan milestones, allocate resources, and schedule tasks. 
  • Prioritize and monitor project tasks with agile development teams using JIRA, ensuring alignment with timelines and objectives. 
  • Maintain control over project budgets per SLA, track additional expenditures, and ensure compliance with validation requirements through comprehensive project documentation. 

What we expect: 

  • At least 3 years of relevant work experience demonstrating that you can make things happen. 
  • Compulsory experience in Clinical Trials/Pharma industries (roles: Project Manager, Clinical Trial Coordinator, Project Coordinator) OR in Tech (IT) as Product/Project Manager or Customer Success Manager. 
  • Proficient English and German language skills. 
  • A Bachelor’s degree in Business Administration, Marketing, or a related field. 
  • Strong communication and stakeholder management skills. 
  • Excellent organizational skills and the ability to manage complexity and shifting priorities. 
  • Comfortable balancing big-picture strategy with attention to detail. 
  • Knowledge of Agile frameworks and experience with JIRA/Confluence. 
  • Familiarity with Microsoft Office; data analytics tools are a bonus. 

Why join us? 

  • 3 additional sick days. 
  • Multisport card (full coverage). 
  • Work on a socially significant project in the inspiring Life Sciences domain. 
  • Opportunities for growth and professional development. 
  • Flexible work schedules with remote or office options. 
  • A collaborative and highly qualified team. 
  • Low-bureaucracy environment with an open-door policy. 

How we work: 

  • We prioritize results over rigid working hours, offering flexible start times between 8:00 and 11:00. Client meetings and team calls take priority, but the focus remains on your output. 
  • Our culture values respect, transparency, and positivity. We maintain an open-door policy, encouraging constructive feedback and fostering a supportive work environment. 
  • If you’re ready to make an impact in the Life Sciences industry, we’d love to hear from you! 

You should apply if: 

  • You are motivated, eager to learn, and thrive in an international, collaborative environment. 
  • You take ownership of your work and excel in creative, independent settings. 
  • You are passionate about making an impact and solving meaningful challenges. 
  • You adapt quickly to change and enjoy fast-paced problem-solving. 

You should not apply if: 

  • You prefer strictly defined processes and rigid structures. 
  • You need micromanagement or constant guidance to succeed. 
  • You are not interested in understanding clients’ business needs and products. 
  • You struggle with ambiguity or fear making mistakes and learning from them. 

Blog

April 15, 2026
TMF Blinding: Removing the Complexity of Managing Blinded Studies

Blinded studies are critical for maintaining the integrity of clinical trials. But while the concept is straightforward, the operational reality is often anything but. For many clinical teams, managing blinding means dealing with: This creates a constant burden: Even with strict processes in place, a single misconfiguration can compromise the entire study. TMF Blinding in […]

April 2, 2026
CTMS for CRO Financial Management: Managing Clinical Trial Budgets and Investigator Payments

Financial management is critical because CROs must ensure that clinical trials remain within budget while generating expected revenue. Without proper financial oversight, organizations may experience delayed payments, incorrect invoicing, or reduced project profitability. A CTMS helps CROs maintain financial control and improve operational efficiency. Financial management is one of the most complex operational areas for […]

April 1, 2026
Risk-Based Monitoring (RBM) in Clinical Trials: A Comprehensive Guide to Modern Oversight

For decades, the clinical research industry operated under a manual, labor-intensive oversight model. The gold standard was 100% Source Data Verification (SDV) – a process where Clinical Research Associates (CRAs) traveled to sites to painstakingly cross-reference every data point in a Case Report Form against medical records. However, as trials have become more data-saturated and […]

March 26, 2026
Why MapLight Therapeutics Chose Flex Databases’ CTMS and eTMF

MapLight Therapeutics selected Flex Databases to support its clinical trial operations with an integrated CTMS and eTMF platform. In this interview, the MapLight team shares why they chose Flex Databases, which features stood out during the evaluation process, and how the platform will support efficient trial oversight and long-term clinical operations. What were the key […]

Contact us

Get in touch to discuss compliance, implementation, demos, pricing

We are here for all of your questions! Tell us more about yourself and we will organize a tailored live demo to show how you can power up your clinical trials processes with Flex Databases.