Director Statistical Programming - Oncology
Director Statistical Programming - Oncology

Director Statistical Programming - Oncology

London Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead statistical programming for oncology, ensuring high-quality data analysis and regulatory compliance.
  • Company: Proclinical is a top life sciences recruiter connecting talent with global opportunities.
  • Benefits: Enjoy a dynamic work environment with opportunities for mentorship and professional growth.
  • Why this job: Make a real impact in oncology while collaborating with innovative teams and advancing your career.
  • Qualifications: Bachelor's in Statistics or related field; advanced degree preferred; experience in oncology required.
  • Other info: Join a forward-thinking company that values bold ideas and continuous improvement.

The predicted salary is between 43200 - 72000 £ per year.

We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking a Senior Lead of Statistical Programming with a focus on Oncology. This role involves developing strategies to enhance statistical analysis and reporting, managing programming teams, and ensuring compliance with regulatory standards. The position requires collaboration with various departments to support clinical study designs and global regulatory submissions.

Responsibilities:

  • Collaborate with the Head of Statistical Programming to implement efficient strategies for statistical analysis and reporting.
  • Oversee programming teams to ensure timely and high-quality delivery of analysis datasets and reports.
  • Align programming strategies with regulatory requirements and project objectives.
  • Drive the creation and validation of SAS/R programs for clinical data analysis.
  • Ensure adherence to SOPs and regulatory standards.
  • Partner with Biostatistics, Clinical Development, and other departments to shape study designs and submission strategies.
  • Represent programming in key meetings and lead contributions to global regulatory submissions.
  • Manage the production of submission-ready datasets and documentation.
  • Champion the adoption of advanced analytics and new technologies to enhance efficiency.
  • Develop standardized processes and mentor teams on industry trends.
  • Participate in continuous improvement activities to enhance clinical operations and data analysis.

Key Skills and Requirements:

  • Bachelor's degree in Statistics, Mathematics, Computer Science, or related discipline; advanced degree preferred.
  • Extensive experience in the pharmaceutical industry or clinical research setting, focusing on oncology.
  • Proficient in statistical programming using SAS.
  • Strong understanding of FDA, EMA, ICH regulations, and CDISC standards.
  • Knowledge of the drug development process and electronic submission requirements.
  • Excellent interpersonal, written, and oral communication skills.
  • Strong analytical, project management, and problem-solving skills.
  • Ability to work in a fast-paced and dynamic environment.

Director Statistical Programming - Oncology employer: Proclinical Staffing

Proclinical is an exceptional employer that fosters a culture of innovation and collaboration, particularly in the dynamic field of oncology. With a commitment to employee growth, we offer extensive training and mentorship opportunities, ensuring our team members are at the forefront of industry advancements. Located in a vibrant area, our workplace promotes a healthy work-life balance, making it an ideal environment for bold thinkers eager to make a meaningful impact in the world of science.
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Contact Detail:

Proclinical Staffing Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Director Statistical Programming - Oncology

✨Tip Number 1

Familiarise yourself with the latest advancements in oncology and statistical programming. Being well-versed in current trends and technologies will not only boost your confidence but also demonstrate your commitment to the field during discussions.

✨Tip Number 2

Network with professionals in the pharmaceutical industry, especially those working in oncology. Attend relevant conferences or webinars to connect with potential colleagues and learn about their experiences, which can provide valuable insights for your application.

✨Tip Number 3

Prepare to discuss specific examples of how you've successfully managed programming teams or projects in the past. Highlighting your leadership skills and ability to deliver high-quality results under pressure will set you apart from other candidates.

✨Tip Number 4

Research Proclinical's values and recent projects. Understanding their mission and how they operate will help you tailor your conversations and show that you're genuinely interested in contributing to their goals.

We think you need these skills to ace Director Statistical Programming - Oncology

Statistical Programming (SAS)
Oncology Expertise
Regulatory Compliance (FDA, EMA, ICH)
CDISC Standards Knowledge
Project Management
Data Analysis
Interpersonal Communication
Written and Oral Communication Skills
Team Leadership
Problem-Solving Skills
Analytical Skills
Knowledge of Drug Development Process
Electronic Submission Requirements
Continuous Improvement Methodologies
Mentoring and Training Skills

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Director Statistical Programming position. Tailor your application to highlight your relevant experience in statistical programming, particularly in oncology.

Highlight Relevant Experience: In your CV and cover letter, emphasise your extensive experience in the pharmaceutical industry or clinical research, especially focusing on oncology. Mention specific projects where you developed strategies for statistical analysis and reporting.

Showcase Technical Skills: Clearly outline your proficiency in statistical programming languages like SAS and any experience with R. Include examples of how you've used these skills to drive the creation and validation of programs for clinical data analysis.

Demonstrate Leadership and Collaboration: Since this role involves managing programming teams and collaborating with various departments, provide examples of your leadership experience and how you've successfully partnered with other teams to shape study designs and submission strategies.

How to prepare for a job interview at Proclinical Staffing

✨Showcase Your Technical Expertise

Make sure to highlight your proficiency in statistical programming, especially with SAS and R. Be prepared to discuss specific projects where you applied these skills, particularly in oncology, as this will demonstrate your capability to handle the technical demands of the role.

✨Understand Regulatory Standards

Familiarise yourself with FDA, EMA, ICH regulations, and CDISC standards. During the interview, be ready to explain how you have ensured compliance in past roles, as this is crucial for the position.

✨Demonstrate Leadership Skills

Since the role involves managing programming teams, share examples of how you've successfully led teams in the past. Discuss your approach to mentoring and developing team members, as well as how you drive collaboration across departments.

✨Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving abilities and project management skills. Prepare to discuss specific challenges you've faced in clinical research and how you overcame them, particularly in fast-paced environments.

Director Statistical Programming - Oncology
Proclinical Staffing
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