You oversee statistical tasks for trials, collaborating with various teams to ensure high-quality deliverables and drive innovative trial designs while engaging with external stakeholders.
Anforderungen
- •PhD with 3+ years’ experience preferred
- •MS with 7+ years’ experience preferred
- •Fluent English (oral and written)
- •Strong communication and presentation skills
- •Automation
- •Biostatistics
- •Clinical Trials
- •Computer Programming
- •Metadata Management
- •Statistical Analysis
Deine Aufgaben
- •Manage all statistical tasks for assigned trials.
- •Develop protocols and statistical analysis plans.
- •Plan and execute statistical analyses with teams.
- •Implement innovative trial designs with Lead Statistician.
- •Drive quantitative decision making with cross-functional teams.
- •Ensure quality and timeliness of statistical deliverables.
- •Engage with external consultants and advisory boards.
Original Beschreibung
# Principal/Senior principal Biostatistician
**Basel (City)** | **Full time**
**Band**
Level 4
**Job Description Summary**
We are in search of a Principal/Senior Principal Biostatistician to join a passionate team in late development. Come to an industry leader where you will lead implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study or project level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners in the early development analytics team.
**Job Description**
**Your Key Responsibilities:**
* Responsible for all statistical tasks on the assigned trials.
* Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
* Contribute to planning and execution of statistical analyses and statistical consultation within your cross-functional teams.
* Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
* Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
* Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
* Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings
**Role Requirements:**
**Essential Requirements:**
* PhD with 3+ years’ experience preferred OR MS with 7+ years’ experience
* Fluent English (oral and written)
* Strong communication and presentation skills
**Skills Desired**
Automation, Biostatistics, Clinical Trials, Computer Programming, Metadata Management, Statistical Analysis