Staburo @ B2Run2019

Staburo @ B2Run2019

Staburo @ B2Run2019 

Team spirit, speed and strength – this time in action! Staburo started again at this year’s B2Run, after the last one in 2018 was canceled due to safety concerns (click here for the story).

With best weather conditions, 30,000 participants from 1,500 Munich companies ran together to finish in the Olympic Stadium. The race track was 6.1km long and took us through the picturesque 1972 Olympic Park, which alone was worth the effort. Staburo was in the middle of the action, and once again no. 1 in the Biostatistics category, check this graph for our results:

Everyone finished safely (after being cheered on, by great Staburo fans before the finish line) and was greeted and congratulated by the rest of the team. Great achievement!

After some alcohol-free electrolytes, water and fruits, we walked to our beautiful location for dinner, the Italian restaurant “Ciao Francesco” with delicious food.

It was a great evening with sports, fun and dinner!

Data analysis, clinical biostatistics and more.

Staburo Data Manager Munich

Staburo Data Manager Munich

Staburo GmbH is a biostatistics company, specialized in statistical consulting, data management and programming for healthcare projects. Based on our 6 pillars (Clinical Statistics, Translational Medicine & Biomarkers, Pharmacokinetics/-dynamics, Health Technology Assessment, Non-clinical Statistics and Statistical Programming with CDISC), we develop tailor-made client solutions. Our customers are international pharmaceutical companies (7 of the top 20), CROs and biotech companies, with whom we work on a flexible basis.

To expand our team in Munich, we are looking for a

Data Manager (f/m/d)

Your responsibilities will include:

  • Identify disclosure-relevant studies within Clinical Trial Management System
  • Review study protocols/amendments for disclosure readiness and provide feedback
    • Ensure compatibility with registry format and content requirements
  • Prepare study data for registration
  • Resolve all study data-related issues with sponsor teams
  • Coordinate approvals for public posting with client
  • Timely submission of registrations
  • Timely update of registry records (incl. protocol amendment information)
  • Resolution of registry NIH QA comments

Your profile:

  • Studies in data management, medical writing, statistics, mathematics, or a similar direction
  • General knowledge of required tasks, willingness to learn
  • Work experience in CRO or pharma/biotech is a plus
  • Fast comprehension and analytical thinking
  • Teamwork and a high degree of initiative

What we offer you:

You can expect an environment with very good development opportunities. We value communication, flat hierarchies, open corporate culture and a harmonious work environment. Our location in Munich offers very good working conditions, modern office space and fast access to public transport.

Curious?

Check our website: www.staburo.de and become part of our constantly growing team!
We look forward to receiving your application, your electronic short CV would be enough for the beginning. Please send this by e-mail to: bewerbung@staburo.de. We look forward to meeting you soon!

Here you find our jod advertisement in PDF format.

 

Staburo Disclosure Manager Munich

Staburo Disclosure Manager Munich

Staburo GmbH is a biostatistics company, specialized in statistical consulting, data management and programming for healthcare projects. Based on our 6 pillars (Clinical Statistics, Translational Medicine & Biomarkers, Pharmacokinetics/-dynamics, Health Technology Assessment, Non-clinical Statistics and Statistical Programming with CDISC), we develop tailor-made client solutions. Our customers are international pharmaceutical companies (7 of the top 20), CROs and biotech companies, with whom we work on a flexible basis.

To expand our team in Munich, we are looking for a

Disclosure Manager (f/m/d)

Your responsibilities will include:

  • Identify disclosure-relevant studies within Clinical Trial Management System
  • Review study protocols/amendments for disclosure readiness and provide feedback
    • Ensure compatibility with registry format and content requirements
  • Prepare study data for registration
  • Resolve all study data-related issues with sponsor teams
  • Coordinate approvals for public posting with client
  • Timely submission of registrations
  • Timely update of registry records (incl. protocol amendment information)
  • Resolution of registry NIH QA comments

Your profile:

  • Studies in data management, medical writing, statistics, mathematics, or a similar direction
  • General knowledge of required tasks, willingness to learn
  • Work experience in CRO or pharma/biotech is a plus
  • Fast comprehension and analytical thinking
  • Teamwork and a high degree of initiative

What we offer you:

You can expect an environment with very good development opportunities. We value communication, flat hierarchies, open corporate culture and a harmonious work environment. Our location in Munich offers very good working conditions, modern office space and fast access to public transport.

Curious?

Check our website: www.staburo.de and become part of our constantly growing team!
We look forward to receiving your application, your electronic short CV would be enough for the beginning. Please send this by e-mail to: bewerbung@staburo.de. We look forward to meeting you soon!

Here you find our jod advertisement in PDF format.

 

Staburo Medical Writer Munich

Staburo Medical Writer Munich

Staburo GmbH is a biostatistics company, specialized in statistical consulting, data management and programming for healthcare projects. Based on our 6 pillars (Clinical Statistics, Translational Medicine & Biomarkers, Pharmacokinetics/-dynamics, Health Technology Assessment, Non-clinical Statistics and Statistical Programming with CDISC), we develop tailor-made client solutions. Our customers are international pharmaceutical companies (7 of the top 20), CROs and biotech companies, with whom we work on a flexible basis.

To expand our team in Munich, we are looking for a

Medical Writer (f/m/d)

Your responsibilities will include:

  • Identify disclosure-relevant studies within Clinical Trial Management System
  • Review study protocols/amendments for disclosure readiness and provide feedback
    • Ensure compatibility with registry format and content requirements
  • Prepare study data for registration
  • Resolve all study data-related issues with sponsor teams
  • Coordinate approvals for public posting with client
  • Timely submission of registrations
  • Timely update of registry records (incl. protocol amendment information)
  • Resolution of registry NIH QA comments

Your profile:

  • Studies in data management, medical writing, statistics, mathematics, or a similar direction
  • General knowledge of required tasks, willingness to learn
  • Work experience in CRO or pharma/biotech is a plus
  • Fast comprehension and analytical thinking
  • Teamwork and a high degree of initiative

What we offer you:

You can expect an environment with very good development opportunities. We value communication, flat hierarchies, open corporate culture and a harmonious work environment. Our location in Munich offers very good working conditions, modern office space and fast access to public transport.

Curious?

Check our website: www.staburo.de and become part of our constantly growing team!
We look forward to receiving your application, your electronic short CV would be enough for the beginning. Please send this by e-mail to: bewerbung@staburo.de. We look forward to meeting you soon!

Here you find our jod advertisement in PDF format.

 

Staburo Senior Statistical Programmer Gdansk

Staburo Senior Statistical Programmer Gdansk

Staburo GmbH is a biostatistics company, specialized in statistical consulting, data management and programming for healthcare projects. Based on our 6 pillars (Clinical Statistics, Translational Medicine & Biomarkers, Pharmacokinetics/-dynamics, Health Technology Assessment, Non-clinical Statistics and Statistical Programming with CDISC), we develop tailor-made client solutions. Our customers are international pharmaceutical companies (7 of the top 20), CROs and biotech companies, with whom we work on a flexible basis.

To expand our team in Gdańsk (Poland), we are looking for a

Senior Statistical Programmer (f/m/d)

Your responsibilities will include:

  • Analysis of clinical studies phases I – IV and presentation of results
  • Statistical programming (SAS with SDTM and ADaM; R)
  • Program validation of clinical trials
  • Specification of analysis datasets
  • SQL, SAS macro programming
  • Direct point of contact for employees and customers

Your profile:

  • University degree in statistics, mathematics, computer science, or equivalent education
  • At least two years of experience in statistical programming and clinical research
  • Excellent working knowledge of clinical trial documents (CSR, SAP, CTR)
  • Very good IT expertise, especially with statistical analysis tools (SAS, R)
  • Quick learning and analytical skills
  • Team player with high degree of initiative
  • Good English skills, German is an advantage

What we offer you:

You can expect an environment with very good development opportunities. We value communication, flat hierarchies, open corporate culture and a harmonious work environment. Our location in Gdańsk offers very good working conditions, modern office space and fast access to public transport.

Curious?

Check our website: www.staburo.de and become part of our constantly growing team!
We look forward to receiving your application, your electronic short CV would be enough for the beginning. Please send this by e-mail to: bewerbung@staburo.de. We look forward to meeting you soon!

Here you find our jod advertisement in PDF format.