Passionate About Advancing Drug Development
Welcome to ThePharmaTeam
Based in Copenhagen, ThePharmaTeam specializes in biostatistics and statistical programming services, delivering high-quality results and solutions tailored to your needs. We are a high-performance team, all with over 20 years of experience in the pharmaceutical industry.
We fully integrate with your organization, empowering you to focus on strategic priorities while we drive progress at all stages of clinical drug development.
Over 20 Years of Global Clinical Development Experience
All members of our team have more than 20 years of experience in the pharmaceutical industry. Our expertise covers clinical trials from Phase 1 through Phase 4, global regulatory submissions, Q&A processes during approval, advisory committee meetings, and post-marketing activities. With our extensive background, we are well-equipped to manage complex projects requiring specialized knowledge in clinical development.
Fully Traceable Solutions in Your Systems
At ThePharmaTeam, we operate as highly efficient in-house consultants, delivering transparent and fully traceable work.
With extensive experience across a wide range of clients, quality systems, and infrastructures, our team seamlessly work with your systems, ensuring smooth collaboration and high-quality tailored results.
Empowering Your Team, Delivering Results from Day One
By partnering with ThePharmaTeam, you gain a team of proactive, self-sufficient consultants who begin making an immediate impact on your project. We integrate with your cross-functional teams, offering expert guidance while independently managing the delivery of high-quality work. This collaborative approach minimizes the need for client oversight, allowing you to focus on your strategic priorities.
The Core Team
Gabriela
Biostatistician
Experienced biostatistician specializing in clinical drug development, with extensive experience in global clinical trials and regulatory submissions. Known for strong leadership and collaboration skills, Gabriela excels in driving projects forward while ensuring integration with cross-functional teams.
Bettina
Programmer
A skilled SAS Solution Specialist and Statistical Programmer with in-depth expertise in CDISC standards (SDTM & ADaM), including data conversion and the development of tools for clinical trial reporting. Bettina is self-driven, quality-focused, and excels in collaborating across multidisciplinary teams to deliver precise, reliable results.
Gitte
Programmer
A highly experienced statistical programmer with deep expertise in clinical trials, safety deliverables, and regulatory submissions. Gitte combines strong programming skills with project management capabilities and exceptional attention to detail, ensuring high-quality deliverables throughout the clinical development process.
Jens-Kristian
Biostatistician
An experienced biostatistician in clinical drug development, Jens-Kristian brings strong statistical and programming expertise combined with an efficient, solution-focused approach to problem solving. Known for delivering accurate and timely results.
CVR: 42366358
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