At a Glance
- Tasks: Manage clinical trials, ensuring compliance and effective execution from start to finish.
- Company: Join Blue Earth Diagnostics, a leader in innovative cancer imaging technologies.
- Benefits: Competitive salary, dynamic work environment, and opportunities for professional growth.
- Other info: Collaborative team culture with a focus on innovation and impact.
- Why this job: Make a real difference in cancer care while working with cutting-edge technology.
- Qualifications: Life science or nursing degree and 4 years of clinical trial management experience required.
The predicted salary is between 46000 - 52000 £ per year.
At Blue Earth Diagnostics Ltd, which is part of the Bracco Group, our mission is to transform the clinical management of patients with cancer by developing innovative molecular imaging technologies. Our team is made up of industry leaders in the field of radiopharmaceutical development and commercialization. Blue Earth Diagnostics is a dynamic and growing company with an approved product already on the market in the USA and in Europe, and a development pipeline of diagnostic radiopharmaceuticals.
The Clinical Trial Manager (CTM) is responsible for the management of all aspects of Clinical Trial activities for their assigned Trial(s). This includes the efficient execution of BED sponsored clinical trials in overall compliance with Good Clinical Practice (GCP), Country Regulations and company Standard Operating Procedures (SOPs), according to time and budget.
Responsibilities:
- In accordance with Blue Earth Diagnostics SOPs: plan, implement, monitor and report on progress against project plans and revise/update as necessary throughout the lifetime of the study.
- Lead the combined study team ensuring effective cross-functional teamwork, while managing trial timelines, budgets, resources, vendors and strategy.
- Work directly with internal teams and external partners to create and proactively manage trial timelines, budgets, resources, vendors and strategy.
- Maintain tracking and provide reports on clinical trial progress against timelines and budget.
- Monitor trial assumptions, schedule and costs to ensure all remain on track with the executed contract(s).
- Act as the primary contact point with CROs, clinical sites and vendors for assigned trial(s).
- Understand the trial delivery strategy, costing assumptions and resulting budget for assigned trial(s) in order to manage vendors.
- Ensure that a robust risk mitigation strategy is in place, regularly monitored for each study, and any issues are escalated as needed to appropriate stakeholders.
- Track and forecast changes in SOW and associated budget including forecasting annual and 5 years planning/spend.
- Other duties as determined by business needs.
Qualifications, Skills and Experience:
- Must have a life science or nursing degree or a similar qualification.
- Must have at least 4 years clinical trial management experience at trial management level on international clinical trials in pharmaceutical and/or CRO industries.
- Oncology clinical trial experience desirable.
- Experience with Radiopharmaceutical clinical trial management highly desirable.
- Knowledge of ICH GCP, international regulatory requirements & guidelines for the conduct of clinical development programs is also a bonus.
- Excellent decision-making, facilitation, communication and organisational skills.
- Ability to work collaboratively on multi-disciplinary project teams and proactively manage relationships with external vendors.
- Ability to influence and build relationships/earn credibility quickly across broad global constituencies with competing priorities.
- Must be able to understand, interpret, and explain protocol requirements to others in a clear and concise manner.
- Must have prior monitoring experience as co-monitoring may be required.
- Experience and skilled with cross-functional and highly matrixed organizations.
- Demonstrated ability to handle multiple competing priorities, utilize resources effectively and adapt flexibly to changing priorities.
- Effective computer skills with good working knowledge of a range of computer programs.
- Team player.
- Change management skills.
Clinical Trial Manager employer: Blue Earth Diagnostics
Contact Detail:
Blue Earth Diagnostics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that Clinical Trial Manager role.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their mission and how your experience aligns with their goals. We want you to show them that you’re not just another candidate, but someone who genuinely cares about transforming cancer management through innovative technologies.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to clinical trial management. We suggest using the STAR method (Situation, Task, Action, Result) to structure your responses. This will help you articulate your experience clearly and effectively.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in keeping you top of mind. And remember, if you see a job that fits your skills on our website, apply directly through us – we’re here to help you succeed!
We think you need these skills to ace Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Manager role. Highlight your relevant experience in clinical trial management, especially in oncology or radiopharmaceuticals. We want to see how your skills align with our mission at Blue Earth Diagnostics!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about transforming cancer care and how your background makes you a perfect fit for our team. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to showcase your decision-making, communication, and organisational skills in your application. We’re looking for someone who can manage multiple priorities and work collaboratively, so let us know how you’ve done this in the past!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at Blue Earth Diagnostics
✨Know Your Stuff
Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and the specific regulations that apply to clinical trials. Familiarise yourself with Blue Earth Diagnostics' mission and their products, especially in the field of radiopharmaceuticals. This will show that you're genuinely interested and prepared.
✨Showcase Your Experience
Be ready to discuss your previous clinical trial management experiences in detail. Highlight any international trials you've managed, particularly in oncology or with radiopharmaceuticals. Use specific examples to demonstrate how you’ve successfully handled timelines, budgets, and vendor relationships.
✨Teamwork Makes the Dream Work
Since the role involves leading a combined study team, be prepared to talk about your experience working collaboratively in multi-disciplinary teams. Share examples of how you've effectively managed relationships with external vendors and internal teams to achieve project goals.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle competing priorities. Think of scenarios where you had to adapt quickly to changes or mitigate risks in a trial. Practising these responses will help you feel more confident during the interview.