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For Companies At a Glance
- Tasks: Lead the review and approval of clinical documents in a dynamic pharmaceutical environment.
- Company: Global Pharmaceutical Company with a focus on innovation and collaboration.
- Benefits: Competitive daily rate, hybrid work model, and opportunities for professional growth.
- Why this job: Make a real impact on clinical trials and contribute to groundbreaking medical advancements.
- Qualifications: Bachelor's degree in science and 5+ years in the pharmaceutical industry required.
- Other info: Join a supportive team with excellent career development opportunities.
The predicted salary is between 72000 - 108000 £ per year.
Job Description
Central Integrated Scientific Review Committee Lead – Global Pharmaceutical Company
Contract: 12 – 18 months
Location: London (Hybrid)
Salary: £360 per day via Umbrella
SRG are working with a Global Pharmaceutical company to help them find a Central Integrated Scientific Review Committee Lead to join their busy team.
The Central Integrated Scientific Review Committee Lead (C-ISRC Lead) plays a key role in the review and approval of clinical documents across therapeutic areas in Development. Key to the role is following documents from C-ISRC submission to finalization, including meeting preparation, meeting management and documentation via minutes for completeness, consistency and process adherence. In collaboration with the C-ISRC Chair and Co-Chair (Clinical Development Head) you will act as project manager in the review cycle and associated activities for high-quality and efficient C-ISRC meeting. Key outcomes are high-quality concept sheets, protocols and clinical development plans.
Key Responsibilities will include:
- Manages C-ISRC Review process for approximately 100+ clinical documents
- each year
- Ensures appropriate C-ISRC documentation and meeting management
- Assists in the development of high-quality protocols and other clinical
- documents via addressing C-ISRC processes/workflow related questions, and
- training and guidance as appropriate
- Works with various systems and trackers to ensure smooth C-ISRC workflow
- (includes CAT, Please Review, Document Management System, etc.); may work
- on system improvement as appropriate
- Serves as back-up to fellow C-ISRC Leads and may attend C-ISRC meetings to
- take minutes or co-facilitate the sessions
- Manages timely key data entry to create reports from appropriate systems
- and facilitate tracking of key metrics for the C-ISRC Office
- May assist in audits and inspection readiness as needed/related to C-ISRC
- process/documentation
- Supports other C-ISRC and Clinical Development projects and activities as
- appropriate (e.g. updating guidance, contributing to trainings and best practice
- sharing, etc.)
Candidate Requirements:
- Minimum Bachelors degree in science; Advanced degree, or equivalent, in science or healthcare preferred.
- 5+ years’ experience in pharmaceutical industry
- Strong knowledge of clinical drug development process, including trial design, GCP, regulatory processes, and clinical project management
- Working knowledge of IT systems and trackers, including Document Management System
- Excellent interpersonal, communication, presentation and meeting management skills
- Advanced medical/scientific writing and communication skills
- Ability to influence wide variety of stakeholders in a matrix environment
Clinical Trial Project Manager employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Project Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for opportunities. A personal recommendation can go a long way in landing that dream role.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Familiarise yourself with their clinical trial processes and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice your communication skills! As a Clinical Trial Project Manager, you'll need to convey complex information clearly. Try mock interviews with friends or use online platforms to refine your pitch and presentation style.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!
We think you need these skills to ace Clinical Trial Project Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Project Manager role. Highlight your experience in managing clinical documents and any relevant project management skills. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the C-ISRC Lead position. Share specific examples of your past experiences that relate to the job description, and don’t forget to show your enthusiasm for joining our team.
Showcase Your Skills: In your application, make sure to highlight your knowledge of clinical drug development processes and any IT systems you’ve worked with. We love seeing candidates who can demonstrate their expertise in these areas, so don’t hold back!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from us during the hiring process!
How to prepare for a job interview at SRG
✨Know Your Stuff
Make sure you brush up on your knowledge of the clinical drug development process. Understand trial design, GCP, and regulatory processes inside out. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.
✨Showcase Your Project Management Skills
Be ready to discuss your experience managing clinical documents and meetings. Prepare specific examples where you've successfully led projects or improved processes. This will demonstrate your capability to handle the responsibilities of a C-ISRC Lead.
✨Familiarise Yourself with Relevant Systems
Since the role involves working with various systems like Document Management Systems and trackers, it’s a good idea to familiarise yourself with these tools. If you have experience with similar systems, be sure to highlight that during the interview.
✨Prepare for Stakeholder Interaction
Given the need to influence a variety of stakeholders, think about how you can demonstrate your interpersonal and communication skills. Prepare scenarios where you've effectively communicated complex information or navigated challenging discussions.
