At a Glance
- 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 be part of a diverse, collaborative team with ongoing training opportunities.
- Why this job: Make a real impact in healthcare while working with cutting-edge technology and a supportive culture.
- Qualifications: Bachelor’s degree or relevant experience; 5+ years in project management; strong communication and problem-solving skills.
- Other info: Familiarity with clinical trials and regulatory standards is a plus.
The predicted salary is between 42000 - 84000 £ per year.
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.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit or follow MMS on LinkedIn .
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.
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Project Manager II (CRO or Life Sciences) - Remote in United Kingdom employer: MMS Holdings Inc
Contact Detail:
MMS Holdings Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Project Manager II (CRO or Life Sciences) - Remote in United Kingdom
✨Tip Number 1
Familiarize yourself with the specific methodologies and processes used in project management within the CRO industry. Understanding the nuances of change management and financial KPIs will help you stand out during discussions.
✨Tip Number 2
Highlight your experience with clinical trials and pharmaceutical development in your conversations. Be prepared to discuss specific projects where you successfully managed timelines and budgets, as this is crucial for the role.
✨Tip Number 3
Network with professionals in the life sciences and CRO sectors. Engaging with others on platforms like LinkedIn can provide insights into the company culture at MMS and may even lead to referrals.
✨Tip Number 4
Demonstrate your problem-solving skills by preparing examples of how you've navigated challenges in past projects. Being able to articulate your approach to risk identification and resolution will be key in interviews.
We think you need these skills to ace Project Manager II (CRO or Life Sciences) - Remote in 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 focus on data-driven solutions in the pharmaceutical and biotech industries, as well as their commitment to customer satisfaction.
Tailor Your CV: Make sure your CV highlights relevant experience in project management, particularly 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 showcases your passion for the industry and your understanding of the challenges faced by CROs. Mention specific experiences that demonstrate your problem-solving skills and ability to work collaboratively.
Highlight Relevant Skills: In your application, be sure to highlight your proficiency with MS Office applications, especially Excel, as well as your familiarity with regulatory requirements like ICH and 21 CFR Part 11. These skills are crucial for the Project Manager II position.
How to prepare for a job interview at MMS Holdings Inc
✨Showcase Your Project Management Skills
Be prepared to discuss your experience in project management, especially in the context of clinical trials or pharmaceutical development. Highlight specific projects where you successfully managed budgets, timelines, and team collaboration.
✨Demonstrate Your Understanding of Regulatory Standards
Familiarize yourself with ICH guidelines, 21 CFR Part 11, and ISO standards relevant to the role. Be ready to explain how you have applied these regulations in past projects to ensure compliance and quality.
✨Prepare for Behavioral Questions
Expect questions that assess your problem-solving abilities and teamwork skills. Use the STAR method (Situation, Task, Action, Result) to structure your responses, focusing on how you resolved conflicts or challenges in previous roles.
✨Research MMS and Its Mission
Understand MMS's mission and values, particularly their focus on customer satisfaction and innovative solutions. Be ready to discuss how your personal values align with theirs and how you can contribute to their goals.