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- Tasks: Lead and manage complex projects in the life sciences sector, ensuring timelines and budgets are met.
- Company: Join MMS, a top-rated CRO dedicated to improving lives through innovative data solutions.
- Benefits: Enjoy remote work flexibility and a supportive team culture focused on growth and development.
- Why this job: Be part of a mission-driven company with a 97% customer satisfaction rating and impactful projects.
- Qualifications: Bachelor’s degree or relevant experience; 5+ years in project management; strong communication skills required.
- Other info: Familiarity with clinical trials and regulatory standards is a plus.
The predicted salary is between 42000 - 84000 £ per year.
Project Manager II (CRO or Life Sciences) – Remote in United Kingdom
About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
This is an experienced Project Management position requiring expertise in the support of Biometric deliverables (Data management, Biostatistics, Statistical Programming services).
Responsibilities
- Understands various cost models and develops budgets for moderate complexity projects.
- Ensures financial KPIs are achieved on assigned projects; invoices on-time and ensures alignment with the contracted payment schedule; updates revenue projections on assigned projects. Controls project scope via defined PM methodology and processes for change management.
- Develops moderate complexity project timelines independently.
- Performs advanced functions in MSP. Understands task constraints and conveys critical path milestones to the functional lead. Develops/input into strategies to help achieve timeline expectations.
- Executes day to day activities during the course of a program/project including risk identification, issue escalation and resolution. Collaborates with functional line management to resolve any issues and trends.
- Intermediate excel skills (Hlookup, Vlookup, Pivot Table, etc.).
- Drives customer satisfaction and works to strengthen client relationships. Develops an account growth plan and consults with line manager to achieve a 10% revenue growth annually (minimum). Manages minimum one key account.
- Participates in or leads RFIs/RFPs in collaboration with proposals team. Participates in or leads capabilities meetings – at least 2 annually.
- Participates in or leads bid defenses – at least 1 annually.
- Proficient in Word, Outlook, PowerPoint.
- Proficient in meeting facilitation including scheduling, development of agendas and meeting minutes; works with project leads to ensure meeting objectives are met.
- Understands general requirements: ICH, 21CRF Part 11, and ISO 9001:2000.
Minimum Requirements
- Bachelor’s Degree required, or relevant work experience.
- Minimum of 5 years’ experience in project coordination or project management or similar field required.
- Expert knowledge of scientific principles and concepts.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Good communication skills and willingness to work with others to clearly understand needs and solve problems.
- Excellent problem-solving skills.
- Good organizational and communication skills.
- Familiarity with current ISO 9001 and ISO 27001 standards preferred.
- Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
- Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Project Management and Information Technology
Industries
Pharmaceutical Manufacturing
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Project Manager - United Kingdom employer: MMS
Contact Detail:
MMS Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Project Manager - United Kingdom
✨Tip Number 1
Familiarize yourself with the specific requirements of the pharmaceutical and biotech industries. Understanding the nuances of clinical trials and regulatory submissions will give you an edge in interviews and discussions.
✨Tip Number 2
Network with professionals in the CRO space, especially those who have experience in project management. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends.
✨Tip Number 3
Brush up on your Excel skills, particularly advanced functions like Hlookup, Vlookup, and Pivot Tables. Being able to demonstrate these skills during practical assessments can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your experience with managing budgets and financial KPIs in previous projects. Be ready to provide examples of how you've successfully controlled project scope and managed client relationships.
We think you need these skills to ace Project Manager - United Kingdom
Some tips for your application 🫡
Understand the Company: Before applying, take some time to understand MMS and its mission. Familiarize yourself with their work in the pharmaceutical and biotech industries, as well as their approach to project management and client satisfaction.
Tailor Your CV: Make sure your CV highlights relevant experience in project management, especially in the life sciences or CRO sectors. Emphasize your expertise in managing budgets, timelines, and client relationships, as these are key aspects of the role.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities and requirements listed in the job description. Use examples from your past experiences to demonstrate how you meet the qualifications, particularly in managing complex projects and collaborating with teams.
Highlight Relevant Skills: In your application, be sure to mention your proficiency with MS Office applications, especially Excel, as well as your understanding of ICH guidelines and regulatory requirements. These skills are crucial for the Project Manager position.
How to prepare for a job interview at MMS
✨Showcase Your Project Management Skills
Be prepared to discuss your experience in managing projects, especially in the context of clinical trials or pharmaceutical development. Highlight specific examples where you successfully managed budgets, timelines, and stakeholder communications.
✨Demonstrate Your Knowledge of Regulatory Standards
Familiarize yourself with ICH guidelines, 21 CFR Part 11, and ISO standards relevant to the industry. Be ready to explain how you have applied these regulations in your previous roles to ensure compliance and quality.
✨Highlight Your Problem-Solving Abilities
Prepare to share instances where you identified risks or issues in a project and how you resolved them. This will showcase your critical thinking and ability to maintain project momentum under pressure.
✨Emphasize Communication and Collaboration Skills
Since this role involves working closely with various teams, be ready to discuss how you foster collaboration and maintain strong client relationships. Provide examples of successful teamwork and how you facilitated effective communication among stakeholders.
