At a Glance
- Tasks: Lead the review of critical clinical documents and coordinate with cross-functional teams.
- Company: Join a leading global pharmaceutical company with a focus on innovation.
- Benefits: Competitive daily rate, hybrid work model, and opportunity for professional growth.
- Other info: Dynamic role with excellent career advancement opportunities in a global environment.
- Why this job: Make a real impact in clinical development while collaborating with top industry professionals.
- Qualifications: Bachelor’s degree in Life Sciences and 5 years’ experience in the pharmaceutical industry.
The predicted salary is between 60000 - 70000 £ per year.
PE Global is currently recruiting for a Clinical Document Review Lead on behalf of a leading global pharmaceutical company. This is an excellent opportunity to join a global Clinical Development team, supporting the review, coordination and governance of key clinical documents across multiple therapeutic areas.
Duration: 12-month contract
Rate: £259.36 per day
Location: London (hybrid)
The Role
As the Clinical Document Review Lead, you will oversee the end-to-end review process for critical clinical development documents, including concept sheets, study protocols and clinical development plans. Acting as the central coordinator for the scientific review process, you will work closely with senior clinical leaders and cross-functional teams to ensure documents are reviewed efficiently, meetings are well managed and governance processes are followed. This is a highly collaborative role that combines project management, stakeholder engagement and clinical document oversight to support the delivery of high-quality clinical programmes.
Key Responsibilities
- Manage the review lifecycle for a high volume of clinical development documents.
- Coordinate document submissions, review timelines and stakeholder communications.
- Prepare and facilitate scientific review meetings, ensuring accurate agendas, documentation and meeting minutes.
- Provide guidance on document review processes, workflows and governance requirements.
- Maintain document management systems, collaborative authoring platforms and tracking tools.
- Produce key performance metrics and support reporting activities.
- Contribute to process improvements, training initiatives and best practice sharing.
- Support audit and inspection readiness through robust documentation and process compliance.
Requirements
- Bachelor’s degree in Life Sciences or a related scientific discipline (advanced degree preferred).
- Minimum 5 years’ experience within the pharmaceutical industry.
- Strong knowledge of clinical drug development, clinical trial design, GCP and regulatory requirements.
- Experience managing clinical documents and review processes within Clinical Development.
- Familiarity with document management systems and collaborative authoring tools.
- Excellent organisational, communication and stakeholder management skills.
- Strong scientific writing, meeting facilitation and project coordination experience.
- Ability to work effectively within a global, cross-functional environment.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK. Interested candidates should submit an updated CV. Please click the link below to apply.
Clinical Document Review Lead employer: PE Global (UK)
PE Global is an exceptional employer, offering a dynamic work environment in the heart of London where collaboration and innovation thrive. As a Clinical Document Review Lead, you will benefit from a hybrid working model, competitive daily rates, and opportunities for professional growth within a leading global pharmaceutical company. Join a team that values your expertise and fosters a culture of continuous improvement and excellence in clinical development.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Document Review Lead
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like PE Global (UK).
We think you need these skills to ace Clinical Document Review Lead
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at PE Global (UK).
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at PE Global (UK). This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at PE Global (UK)
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with PE Global (UK).
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help PE Global (UK) achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
