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- Aufgaben: Lead complex clinical studies and develop strategies for drug development.
- Arbeitgeber: Join a dynamic team focused on innovative drug development and patient value.
- Mitarbeitervorteile: Flexible part-time/full-time options with opportunities for career growth.
- Warum dieser Job: Make a real impact in oncology while collaborating with diverse teams.
- Gewünschte Qualifikationen: Ph.D. or MS in Statistics/Biostatistics with 8+ years in Pharma/Biotech.
- Andere Informationen: Represent Biostatistics in external partnerships and improve departmental standards.
Das voraussichtliche Gehalt liegt zwischen 72000 - 108000 € pro Jahr.
Your role:
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 for developing 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 include contributing to the integrated evidence plan for a drug development program to create value for patients and support marketing authorization and reimbursement, and providing statistical leadership in the development of human research study designs while taking accountability for statistical matters in matrix leadership of other statisticians. You will ensure that statistical analyses are effectively performed and conducted with 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.
Who you are:
- Ph.D. or MS in Statistics, Biostatistics or related discipline
- Excellent team player (both within the project and within the function), strong communication and influencing skills, fluent in English
- Experience working in a diverse, global working environment
- At least 8 years of experience in the Pharmaceutical/Biotechnology industry in clinical development
- Comprehensive expertise in drug development, including knowledge of interfaces and interdependencies with other functions
- Excellent knowledge of relevant guidance documents (from ICH, FDA, EMA, etc.), using them proactively to impact performance or find alternative solutions
- Strong leadership competencies: purposeful, results-driven, innovative, collaborative, future-oriented
- Experience in oncology preferred
Department: HC-RD-BAOL Biostatistics Oncology Late Development
Job Evaluation: AT – Expert 4 #J-18808-Ljbffr
Director Biostatistics (all genders) - part-time/full-time Arbeitgeber: Merck Group
Kontaktperson:
Merck Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Director Biostatistics (all genders) - part-time/full-time
✨Tip Number 1
Network with professionals in the pharmaceutical and biotechnology industries, especially those who have experience in biostatistics and oncology. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in drug development.
✨Tip Number 2
Showcase your leadership skills by participating in relevant projects or initiatives within your current role. Highlight any experiences where you led a team or contributed to significant decision-making processes, as this will demonstrate your capability to take on a director-level position.
✨Tip Number 3
Familiarize yourself with the latest guidance documents from ICH, FDA, and EMA. Being able to discuss how you have applied these guidelines in past projects can set you apart during interviews and show your proactive approach to regulatory compliance.
✨Tip Number 4
Prepare to discuss your experience with complex clinical studies and how you've successfully communicated statistical analyses to both technical and non-technical audiences. This will be crucial in demonstrating your ability to bridge gaps between different stakeholders in the drug development process.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Director Biostatistics (all genders) - part-time/full-time
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and qualifications required for the Director Biostatistics position. Tailor your application to highlight how your experience aligns with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in the Pharmaceutical/Biotechnology industry, particularly in clinical development and oncology. Provide specific examples of complex studies you have led and the impact of your statistical leadership.
Showcase Communication Skills: Since strong communication skills are essential for this role, include examples of how you have effectively communicated complex statistical concepts to both technical and non-technical audiences. This could be through presentations, reports, or collaborative projects.
Prepare a Strong Cover Letter: Craft a compelling cover letter that not only summarizes your qualifications but also expresses your passion for drug development and your commitment to evidence-based decision-making. Make sure to convey your enthusiasm for contributing to patient value and supporting marketing authorization.
Wie du dich auf ein Vorstellungsgespräch bei Merck Group vorbereitest
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience in biostatistics and drug development in detail. Highlight specific projects where you led complex clinical studies or contributed to evidence generation strategies, as this will demonstrate your capability to handle the responsibilities of the role.
✨Emphasize Team Collaboration
Since the role requires working in cross-functional teams, share examples of how you've successfully collaborated with diverse groups. Discuss your communication style and how you influence others, as these skills are crucial for a leadership position.
✨Familiarize Yourself with Regulatory Guidelines
Make sure you are well-versed in relevant guidance documents from ICH, FDA, and EMA. Be ready to discuss how you've applied these guidelines in past projects to improve performance or navigate challenges, showcasing your proactive approach.
✨Prepare for Technical and Non-Technical Communication
Since you'll need to communicate statistical analyses to both technical and non-technical audiences, practice explaining complex concepts in simple terms. This will help demonstrate your ability to ensure objective interpretation of study results.
