Director Biostatistics (all genders) - part-time/full-time at Merck Group
Darmstadt, Hessen, Germany -
Full Time


Start Date

Immediate

Expiry Date

13 May, 25

Salary

0.0

Posted On

14 Feb, 25

Experience

0 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Responsibilities

You will play a key role in the success of drug development, as part of a team that encourages career growth and development. As a statistical leader working in a cross-functional team, you will be responsible to develop an appropriate strategy for evidence generation to create value in a drug development program and to support evidence-based decision-making. You may independently lead very complex clinical studies or one or more oncology drug development projects in study design, data analysis and interpretation of results, authoring regulatory responses and other documents with minimal supervision. Key responsibilities will be to contribute to the integrated evidence plan for a drug development program to create value for patients and support marketing authorization and reimbursement, and to provide statistical leadership in the development of human research study designs and take accountability for statistical matters, in matrix leadership of other statisticians. You will ensure that statistical analyses are effectively performed and conducted in high quality and in a timely manner and communicated to both technical and non-technical audiences. You will ensure the objective interpretation of human research study results to support informed decision-making. Furthermore, you will represent Biostatistics externally, e.g. in interactions with Health Authorities and external partnerships, and support the development of departmental standards and process improvements.

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