Delivery Manager – Drug Development

🕒 March 20

🇵🇱 Poland – Remote

💵 zł18k - zł22k / month

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 38%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Appsilon

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2013

🏥 Healthcare

💼 Consulting

💊 Pharmaceuticals

Healthcare • Consulting • Pharmaceuticals

Appsilon is a technology company that partners with life sciences and pharmaceutical organizations to build open-source, validated data analytics and visualization solutions using R, Python, and Shiny. They provide cloud-native Statistical Computing Environments (SCEs), GxP-compliant infrastructure, Axon. R validation tooling, and SAS-to-open-source migration to accelerate clinical development, regulatory submissions, and enterprise analytics in highly regulated settings. Appsilon delivers B2B services combining software engineering, data science, and AI to produce production-grade clinical apps, dashboards, and automation for pharmaceutical and life sciences companies.

📋 Description

• Lead data-focused projects for pharma and biotech clients, especially those related to clinical trials. • Build strong relationships with clients: understand their needs, offer advice, and solve problems. • Ensure clients are satisfied and want to continue working with us. • Work with the Sales team on pre-sales and the Account Management team on cross-sell and upsell opportunities by identifying client needs, providing proactive insights, and leveraging your expertise in clinical trials. • Step in as a Project or Product Manager when needed: manage the backlog, clarify requirements, and support engineers.

🎯 Requirements

• 5+ years of experience in a similar role or in top consulting firms. • Proven track record of leading successful IT projects in pharma/biotech. • Knowledge of CDISC standards (e.g., SDTM, ADaM, SEND) and experience with clinical trial data tools or workflows. • A background in molecular biology or bioinformatics is a strong plus. • Experience in working directly with clients and managing relationships. • Ability to talk to both business and technical people. • High motivation to achieve success, can-do attitude, business maturity, patience, strong communication skills, and a high level of professionalism. • Willingness to travel a few times a year when needed (client visits, conferences, etc.). • English Fluency: C1/C2 level.

🏖️ Benefits

• Fully remote work, with flexibility to collaborate across time zones and adapt working hours to project and client needs. • Time and budget for continuous professional development, including domain knowledge, certifications, and industry events. • Modern equipment (MacBook or ThinkPad with Linux) and tools that enable efficient, high-quality delivery work. • Collaboration with experienced engineers, data scientists, and subject matter experts in a supportive, high-trust environment. • A remote-first culture built on trust, ownership, and kindness, where teams collaborate effectively and take pride in high-quality delivery.