Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead
Senior Regulatory Affairs Specialist - RIM & Submissions

Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead

Maidenhead Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure compliance and prepare submissions for regulatory agencies in a dynamic biopharmaceutical environment.
  • Company: Leading biopharmaceutical company in Maidenhead with a people-first culture.
  • Benefits: Inclusive workplace, opportunities for innovation, and career development.
  • Why this job: Join a team committed to making a difference in healthcare through regulatory excellence.
  • Qualifications: Experience in Regulatory Information Management and proficiency in MS Office required.

The predicted salary is between 36000 - 60000 £ per year.

A leading biopharmaceutical company in Maidenhead is seeking a Sr. Associate in Regulatory Affairs. The role involves ensuring compliance with data standards, preparing submissions to regulatory agencies, and maintaining data integrity.

Ideal candidates will have:

  • Experience in Regulatory Information Management
  • A bachelor's degree
  • Proficiency in MS Office applications

The company prides itself on a people-first culture and a commitment to innovation and inclusivity.

Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead employer: Alnylam Pharmaceuticals

As a leading biopharmaceutical company in Maidenhead, we offer a dynamic work environment that prioritises employee well-being and fosters a culture of innovation and inclusivity. Our commitment to professional development ensures that our team members have ample opportunities for growth, while our people-first approach creates a supportive atmosphere where every voice is valued.
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Contact Detail:

Alnylam Pharmaceuticals Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors for you.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of regulatory submissions and data standards. We recommend practising common interview questions and having examples ready that showcase your experience in Regulatory Information Management.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values. Since this role is with a people-first culture, make sure to highlight your commitment to inclusivity and innovation during your conversations.

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us.

We think you need these skills to ace Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead

Regulatory Information Management
Data Standards Compliance
Submission Preparation
Data Integrity Maintenance
Bachelor's Degree
MS Office Proficiency
Attention to Detail
Communication Skills
Problem-Solving Skills
Knowledge of Regulatory Agencies

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Regulatory Information Management and any relevant submissions you've worked on. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs and how you can contribute to our people-first culture. Keep it concise but impactful – we love a good story!

Showcase Your MS Office Skills: Since proficiency in MS Office applications is key for this role, make sure to mention any specific projects or tasks where you’ve used these tools effectively. We appreciate candidates who can demonstrate their technical skills!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our innovative team!

How to prepare for a job interview at Alnylam Pharmaceuticals

✨Know Your Regulatory Stuff

Make sure you brush up on your knowledge of Regulatory Information Management and the latest compliance standards. Familiarise yourself with the specific regulations that apply to the biopharmaceutical industry, as this will show your potential employer that you're serious about the role.

✨Showcase Your Submission Skills

Prepare examples of past submissions you've worked on. Be ready to discuss the challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving abilities, which are crucial for the position.

✨Highlight Your People Skills

Since the company values a people-first culture, be prepared to talk about how you collaborate with others. Share stories that illustrate your ability to work in teams, communicate effectively, and contribute to an inclusive environment.

✨Get Comfortable with MS Office

Proficiency in MS Office is a must, so make sure you're familiar with the tools you'll be using daily. Consider preparing a quick demo or example of how you've used these applications in your previous roles to streamline processes or enhance data integrity.

Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead
Alnylam Pharmaceuticals
Location: Maidenhead
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  • Senior Regulatory Affairs Specialist - RIM & Submissions in Maidenhead

    Maidenhead
    Full-Time
    36000 - 60000 £ / year (est.)
  • A

    Alnylam Pharmaceuticals

    201-500
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