In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham
In-House Clinical Research Associate – Freelance – UK Biotech

In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham

Birmingham Freelance 35000 - 45000 £ / year (est.) No home office possible
Apsida Life Science

At a Glance

  • Tasks: Join a dynamic team to ensure successful execution of clinical trials in oncology.
  • Company: Innovative biotech firm focused on advancing cutting-edge therapies.
  • Benefits: Freelance contract with competitive pay and the chance to make a real impact.
  • Why this job: Be part of groundbreaking research that improves patient outcomes globally.
  • Qualifications: Bachelor's in Life Sciences and 2+ years in clinical research required.
  • Other info: Opportunity for travel and collaboration with top professionals in the field.

The predicted salary is between 35000 - 45000 £ per year.

Apsida Life Science are currently partnered with an innovative clinical-stage biotech organisation dedicated to advancing cutting-edge therapies in oncology. With a strong and growing clinical pipeline, the company is committed to delivering impactful treatments that improve patient outcomes globally.

As part of their continued growth, they are now seeking an In-House Clinical Research Associate (IHCRA) to join their Clinical Operations team. This is an excellent opportunity to play a key role in ensuring the successful execution of clinical trials, working cross-functionally with internal teams and external partners.

Responsibilities:
  • Site Feasibility Process
  • Reviews critical factors for site selection with Medical Science staff and Clinical Trial Manager
  • Reviews site feasibility/qualification reports from CRO to ensure evidence-based site assessments
  • Act as a QC reviewer for key study documentation including protocols, informed consent forms, and study materials
  • Attends CRO CRA meetings periodically to provide further support and training to CRAs, and to gain insight into study challenges at site level
  • Recruitment support initiatives (such as direct to coordinator enrolment calls, newsletters, flyer preparation) in collaboration with clinical operations and clinical science
  • Reviews protocol deviation trends and works with Clinical Trial Manager to communicate expected actions to the CRO
Requirements:
  • Bachelor’s degree in Life Sciences
  • Minimum 2+ years of experience in clinical research, including site monitoring experience
  • Strong understanding of ICH-GCP guidelines and clinical trial regulations
  • Experience in oncology clinical research is highly desirable
  • Familiarity with clinical systems, databases, and project management tools
  • Excellent organisational skills with the ability to manage multiple priorities
  • Willingness to travel up to 25%

If you are interested in learning more, please reach out to Nicole Skinner at Apsida Life Science: www.apsida.co.uk +44 74413 41417

Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry.

In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham employer: Apsida Life Science

Apsida Life Science is an exceptional employer, offering a dynamic work environment where innovation in clinical research thrives. With a strong commitment to employee growth and development, team members are encouraged to collaborate across functions and contribute to impactful oncology therapies. Located in the vibrant biotech hub of the UK, employees benefit from a supportive culture that values their contributions and fosters professional advancement.
Apsida Life Science

Contact Detail:

Apsida Life Science Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham

Tip Number 1

Network like a pro! Reach out to your connections in the biotech field, especially those who work in clinical research. A friendly chat can lead to insider info about job openings or even referrals.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and oncology research. We recommend practising common interview questions with a friend to boost your confidence.

Tip Number 3

Showcase your organisational skills! During interviews, share examples of how you've managed multiple priorities in past roles. This will demonstrate your ability to handle the demands of an IHCRA position.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals to join our team in advancing clinical research.

We think you need these skills to ace In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham

Site Feasibility Assessment
Clinical Trial Management
Quality Control Review
Protocol Development
Informed Consent Documentation
Oncology Clinical Research
ICH-GCP Guidelines
Clinical Research Regulations
Project Management Tools
Organisational Skills
Cross-Functional Collaboration
Recruitment Support Initiatives
Data Analysis
Communication Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the In-House Clinical Research Associate role. Highlight your relevant experience in clinical research and oncology, and don’t forget to showcase your understanding of ICH-GCP guidelines!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your skills align with the company’s mission to improve patient outcomes. Keep it concise but impactful!

Showcase Your Organisational Skills: Since the role requires excellent organisational skills, provide examples in your application that demonstrate how you’ve successfully managed multiple priorities in past roles. We love seeing real-life examples!

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates!

How to prepare for a job interview at Apsida Life Science

Know Your Stuff

Make sure you brush up on your knowledge of ICH-GCP guidelines and clinical trial regulations. Being able to discuss these confidently will show that you're not just familiar with the basics, but that you truly understand the intricacies of clinical research.

Showcase Your Experience

Prepare specific examples from your past roles that highlight your site monitoring experience and any challenges you've faced in oncology research. This will help demonstrate your problem-solving skills and how you can contribute to the team.

Ask Smart Questions

Come prepared with insightful questions about the company's clinical pipeline and their approach to site feasibility. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Be Organised

Since the role requires excellent organisational skills, make sure to present yourself as such during the interview. Bring a well-organised portfolio of your work, and be ready to discuss how you manage multiple priorities effectively.

In-House Clinical Research Associate – Freelance – UK Biotech in Birmingham
Apsida Life Science
Location: Birmingham

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