Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical trials, manage data quality, and ensure regulatory compliance.
- Company: Join a pioneering team dedicated to advancing science and making a real-world impact.
- Benefits: Enjoy flexible work options, competitive salary, and opportunities for professional growth.
- Why this job: Be part of groundbreaking research in rare diseases and collaborate with diverse teams.
- Qualifications: Expertise in SAS, R programming, and strong knowledge of clinical regulations required.
- Other info: Ideal for innovative thinkers eager to make a difference in healthcare.
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. The role drives strategic input into clinical study design, ensures excellence in data management, and supports successful regulatory submissions. You will work independently on multiple projects, leading trials in rare diseases and overseeing timelines and quality control.
Key Responsibilities:
- Provide statistical expertise in clinical planning, study design, and protocol development.
- Develop statistical analysis methodologies and plans.
- Perform blinded in-trial data quality reviews and pre-database lock data quality control.
- Oversee the preparation and integration of clinical regulatory submission packages.
- Collaborate with cross-functional teams including clinicians, clinical operations, and regulatory affairs.
- Lead and drive submissions, ensuring adherence to regulatory requirements.
Required Skills:
- Expertise in SAS and R programming for data management and statistical analysis.
- Proficiency in MS Word, Excel, and PowerPoint.
- Sound knowledge of clinical and statistical regulatory requirements.
- Ability to manage multiple clinical trials and oversee quality control processes.
Senior Associate/Manager, Regulatory Sciences employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Associate/Manager, Regulatory Sciences
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trial design, especially for rare diseases. This knowledge will not only help you stand out during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in regulatory sciences through platforms like LinkedIn or industry conferences. Engaging with others in the field can provide valuable insights and potentially lead to referrals that could enhance your application.
✨Tip Number 3
Showcase your expertise in SAS and R programming by discussing specific projects where you've applied these skills. Be prepared to explain how your statistical analysis methodologies have contributed to successful outcomes in previous roles.
✨Tip Number 4
Prepare for the interview by reviewing common questions related to clinical study design and regulatory submissions. Practising your responses will help you articulate your experience and demonstrate your ability to lead and manage multiple projects effectively.
We think you need these skills to ace Senior Associate/Manager, Regulatory Sciences
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Senior Associate/Manager, Regulatory Sciences position. Make sure you understand the key responsibilities and required skills, such as expertise in SAS and R programming, and how they relate to your experience.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical study design, data management, and regulatory submissions. Use specific examples that demonstrate your statistical expertise and ability to manage multiple projects effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pushing the boundaries of science. Discuss how your background aligns with the company's mission and the specific requirements of the role, particularly your experience with rare diseases and cross-functional collaboration.
Proofread and Edit: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your writing is clear and professional, reflecting your attention to detail, which is crucial for this role.
How to prepare for a job interview at Proclinical Staffing
✨Showcase Your Statistical Expertise
Be prepared to discuss your experience with SAS and R programming. Highlight specific projects where you developed statistical analysis methodologies or conducted data quality reviews, as this will demonstrate your technical proficiency.
✨Demonstrate Leadership in Clinical Trials
Share examples of how you've led clinical trials, particularly in rare diseases. Discuss your approach to managing timelines and ensuring quality control, as this aligns with the responsibilities of the role.
✨Understand Regulatory Requirements
Familiarise yourself with the latest regulatory requirements relevant to clinical studies. Be ready to discuss how you ensure adherence to these regulations during submissions, showcasing your knowledge and attention to detail.
✨Collaborate Effectively
Prepare to talk about your experience working with cross-functional teams. Provide examples of successful collaborations with clinicians, clinical operations, and regulatory affairs, emphasising your ability to drive projects forward.
