Clinical Study Report – Clinical Pharmacology
Clinical Study Report – Clinical Pharmacology

Clinical Study Report – Clinical Pharmacology

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

  • Tasks: Write and prepare Clinical Study Reports for Phase 1, ensuring compliance with regulatory guidelines.
  • Company: Join a leading client in the clinical research field with a focus on innovation.
  • Benefits: Flexible working arrangements and opportunities for professional growth.
  • Why this job: Make a real impact in clinical research while honing your scientific writing skills.
  • Qualifications: Strong report writing experience and attention to detail required.
  • Other info: Ideal for freelancers or those looking to enter the clinical study sector.

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

Clinical Study Report (CSR) Writing

We have an amazing client looking for a CSR Writer to support a full Clinical Study Report writing for Phase 1, development and preparation of regulatory Modules (2.7.1/2.7.2). They are looking for strong scientific writing skills, a key attention to detail and inspection‑ready deliverables.

Key Responsibilities

  • All deliverables are inspection ready and compliant with regulatory guidelines
  • Maintain planning for writing and QC deliverables
  • Highlight any process improvements to enhance collaboration between CPP and document Service Teams
  • Excel in shell creation and timeline management
  • Create QC reports
  • Interpret clinical and statistical outputs

Skills

  • Strong experience in report writing and QC procedures
  • Formal communication skills
  • Excellent knowledge of formatting on Word

An Ideal Candidate

  • Understanding of PK/PD analysis tools
  • Working understanding of Phoenix WinNonlin

If you are a contract freelancer in CSR or looking to move into this sector please apply below and I would love to hear from you to discuss the vacancy further.

Clinical Study Report – Clinical Pharmacology employer: Barrington James Limited

Join a dynamic and innovative team that values scientific excellence and attention to detail in the heart of the pharmaceutical industry. Our client offers a collaborative work culture, opportunities for professional growth, and the chance to contribute to impactful clinical research projects. With a focus on regulatory compliance and quality deliverables, this role provides a meaningful pathway for those looking to advance their careers in clinical pharmacology.
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Contact Detail:

Barrington James Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Study Report – Clinical Pharmacology

Tip Number 1

Network like a pro! Reach out to professionals in the clinical pharmacology field on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities that aren’t even advertised.

Tip Number 2

Prepare for interviews by brushing up on your scientific writing skills and understanding regulatory guidelines. We recommend practising common interview questions related to CSR writing, so you can showcase your expertise confidently.

Tip Number 3

Don’t forget to tailor your approach! When applying through our website, make sure to highlight your attention to detail and any relevant experience with PK/PD analysis tools. We want to see how you can bring value to the team!

Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We believe it shows your enthusiasm and professionalism, which are key traits for a CSR Writer.

We think you need these skills to ace Clinical Study Report – Clinical Pharmacology

Clinical Study Report Writing
Regulatory Compliance
Attention to Detail
Scientific Writing Skills
Quality Control Procedures
Formal Communication Skills
Word Formatting
PK/PD Analysis Tools
Phoenix WinNonlin
Timeline Management
Collaboration Skills
Process Improvement

Some tips for your application 🫡

Show Off Your Writing Skills: Make sure your application highlights your scientific writing prowess. We want to see examples of your previous work, especially if it relates to Clinical Study Reports or similar documents. Don’t hold back on showcasing your attention to detail!

Tailor Your Application: Customise your CV and cover letter to reflect the specific requirements mentioned in the job description. We love it when candidates align their experiences with what we’re looking for, so make it clear how you fit the bill!

Be Inspection-Ready: Since we’re all about compliance and inspection-ready deliverables, ensure your application is polished and free from errors. We appreciate a well-formatted document, so pay attention to the details in your submission.

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 don’t miss out on any important updates. Plus, it shows you’re keen to join our team!

How to prepare for a job interview at Barrington James Limited

Master the Basics of CSR Writing

Before your interview, brush up on the fundamentals of Clinical Study Report writing. Familiarise yourself with the structure and key components of a CSR, especially for Phase 1 studies. This will show that you understand the role and can hit the ground running.

Showcase Your Attention to Detail

During the interview, be prepared to discuss examples where your attention to detail made a difference in your previous work. Highlight specific instances where you ensured compliance with regulatory guidelines or improved the quality of deliverables. This is crucial for impressing your potential employer.

Demonstrate Your Scientific Writing Skills

Bring along samples of your previous work that showcase your scientific writing abilities. Be ready to explain your writing process and how you ensure clarity and precision in your reports. This will help the interviewer see your capability in producing inspection-ready deliverables.

Familiarise Yourself with Key Tools

Make sure you have a good understanding of PK/PD analysis tools and Phoenix WinNonlin, as these are important for the role. If you have experience using these tools, share that during the interview. If not, do some research to at least demonstrate your willingness to learn and adapt.

Clinical Study Report – Clinical Pharmacology
Barrington James Limited

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