At a Glance
- Tasks: Lead and manage ophthalmology clinical development programmes from start to finish.
- Company: Join a pioneering biotech firm focused on innovative healthcare solutions.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic role with potential for career advancement in a collaborative environment.
- Why this job: Make a real difference in patient care while developing your project management skills.
- Qualifications: Degree in Life Sciences or related field; experience in clinical settings preferred.
The predicted salary is between 60000 - 75000 £ per year.
Your mission is to lead and oversee the end-to-end planning and execution of MeiraGTx’s ophthalmology clinical development programmes, ensuring alignment across all stages. You will provide regular, clear updates to senior management on pre-clinical & clinical progress, development activities, operational delivery, and regulatory milestones and timelines.
Purpose of Job: Lead day-to-day operational delivery of ophthalmology clinical development programmes, managing complex clinical and CMC workstreams to ensure aligned and timely execution against programme objectives. Drive end-to-end planning and cross-functional coordination across clinical, development, operational, and regulatory activities, leading project teams and acting as the central point of accountability for programme delivery and issue resolution. Serve as the primary point of contact for external partners, funders, and collaborators associated with such programme assets, ensuring clear communication, alignment of expectations, and delivery against agreed milestones. Deliver consistent, high-quality communication to senior management on programme status, key deliverables, risks, and timelines across all stages of the ophthalmology development lifecycle.
Key Responsibilities:
- Programme Leadership: Lead end-to-end delivery of ophthalmology clinical development programmes, ensuring achievement of key milestones across scope, timelines, and budgets, with proactive management of risks, dependencies, and programme complexity.
- Cross-Functional Delivery: Direct and align cross-functional teams (pre-clinical, clinical operations, regulatory, medical writing, biostatistics, and Product Supply) to ensure integrated execution across all stages of the ophthalmology development lifecycle.
- Planning & Risk Management: Develop and maintain integrated programme plans, incorporating robust risk identification, mitigation strategies, and contingency planning to support uninterrupted programme progression.
- Regulatory & Quality Compliance: Ensure adherence to GCP, FDA and EMA requirements, and internal SOPs, embedding quality and regulatory standards across all clinical and development activities.
- Stakeholder Communication: Provide clear, data-driven updates to senior management, ensuring visibility of programme status, key deliverables, risks, and critical decision points across the ophthalmology portfolio.
- External Partner Management: Act as the primary point of contact for external partners, funders, and service providers, ensuring alignment to programme objectives, timelines, and contractual deliverables.
- Milestone & Supply Integration: Oversee critical programme milestones, ensuring alignment between Pre-Clinical, MSAT, Manufacturing, Quality, Product Supply, Regulatory and Clinical delivery to enable seamless transition to clinic.
- Governance & Reporting: Maintain accurate programme documentation and governance frameworks, supporting the preparation of high-quality reports and presentations for the Clinical and Product Supply leadership teams.
- Continuous Improvement: Identify and implement process improvements across programme and supply chain activities to enhance operational efficiency, scalability, and delivery performance.
Key Job Competencies:
- Project & Programme Leadership
- Cross-Functional Leadership
- Strategic Planning & Execution
- Stakeholder Communication & Influencing
- Risk Management & Problem Solving
- Regulatory & Quality Compliance
- Clinical Supply & Delivery
- External Partner Management
Qualifications:
- Bachelor’s degree in Life Sciences, or a related field, or equivalent work experience in supply chain or project/programme management within biotech or pharmaceutical industries.
- Strong understanding of clinical trial design, execution, CMC and regulatory requirements.
- Experience managing timelines, budgets, and resources in a clinical setting.
- Ability to work collaboratively in a global environment.
- PMP or equivalent certification is a plus.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), with the ability to quickly learn new systems.
Project Manager, 24-month FTC employer: Meiragtx
At MeiraGTx, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of ophthalmology clinical development. Our employees benefit from comprehensive professional growth opportunities, competitive remuneration, and a commitment to maintaining high standards of quality and compliance. Located in a vibrant area, we provide a supportive environment where your contributions directly impact the advancement of groundbreaking therapies, making your work both meaningful and rewarding.
StudySmarter Expert Advice🤫
We think this is how you could land Project Manager, 24-month FTC
✨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!
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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 Meiragtx.
We think you need these skills to ace Project Manager, 24-month FTC
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 Meiragtx.
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 Meiragtx. 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 Meiragtx
✨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 Meiragtx.
✨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 Meiragtx 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.
