Central Monitor Intern at Cyntegrity Germany GmbH
Deutschland, , Germany -
Full Time


Start Date

Immediate

Expiry Date

17 May, 25

Salary

0.0

Posted On

18 Feb, 25

Experience

0 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Join Cyntegrity as an intern, one of the leading clinical trial risk management technology providers in the industry. We’re proud of our bespoke and highly rated MyRBQM® Portal and MyRBQM® Academy brands. At Cyntegrity, we specialize in delivering innovative solutions to improve clinical research. Our Data Science team plays a critical role in developing advanced models, analyzing data, and creating algorithms to de-risk clinical trials in the pharmaceutical field. Join us as a Central Monitor intern to gain hands-on experience in the world of data science while contributing to meaningful projects that make a real impact.

WHAT WE’RE LOOKING FOR:

We’re seeking curious, driven, and collaborative individuals who are eager to learn and make an impact. Here’s what you’ll need:

  • Educational Background:
  • Currently pursuing or recently completed a degree in Medicine / Pharmaceutic / Biology / Chemistry.
  • Skills & Tools:
  • Strong analytical and problem-solving skills.
  • Experience with data visualization tools (e.g., Excel, Power Pivot, Power Query).
  • Python coding skills are plus.
  • CRA experience is a plus .
  • Soft Skills:
  • Effective communication skills, both verbal and written.
  • Ability to work independently and as part of a team.A proactive and curious mindset, with a willingness to explore new ideas.

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Responsibilities

As a Central Monitor Intern, you will work alongside our talented team on projects that directly contribute to the success of our clinical trial risk monitoring solutions. Your responsibilities will include:

  • Clinical Trial Data Analysis & Monitoring:
  • Understanding of clinical trial protocols, risk assessment and risk management methods applied for the study.
  • Design/Review metrics (KRI, Acceptable Ranges (ARs)), Subject Profile
  • Design RM monitoring scenario(s) for the clinical trial(s)
  • Analyzing clinical trial data (enrollment, metrics, Risk Indicators (RI), ARs).
  • Using Risk Based monitoring technics prepare the clinical trial status report, propose Investigative Corrective Actions ( ICA) for the Risk escalation improvement, follow up ICA execution and effectiveness.
  • Designing and developing algorithms to support data-driven decision-making.
  • Collaboration & Optimization:
  • Collaborating with team members to review specifications of metrics, key risk indicators, and quality tolerance limits.
  • Proposing optimizations and improvements to existing processes and algorithms.
  • Communication & Reporting:
  • Presenting findings and insights using data visualization tools.
  • Preparing clear and concise reports for internal and client-facing projects.
  • Innovation & Learning:
  • Exploring cutting-edge tools and techniques to enhance data analysis and modeling.Participating in brainstorming sessions to develop innovative solutions.

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