At a Glance
- Tasks: Lead global clinical trials and ensure compliance with regulations.
- Company: Join a dynamic Biotechnology company focused on Oncology.
- Benefits: Flexible remote work, competitive pay, and a chance to make a difference.
- Other info: Work independently in a supportive, collaborative environment.
- Why this job: Be at the forefront of groundbreaking Oncology research and trials.
- Qualifications: 5+ years in clinical project management, especially in Oncology.
The predicted salary is between 43200 - 72000 £ per year.
EPM Scientific are currently partnered with a Biotechnology company who are seeking a Freelance Clinical Project Manager to support their upcoming Oncology Trials in the EU. See a short summary below: Contract Conditions: Start date: ASAP Location: European Union (Remote) Contract: 0.8 - 1 FTE, 12-Month Contract Project: Oncology - Phase 3 Global Trial Key Responsibilities: Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements. Serve as the primary point of contact for internal and external stakeholders, supporting site initiation, monitoring, and close-out activities. Ensure timely and accurate documentation, data collection, and reporting in line with project timelines. Collaborate with cross-functional teams including CRAs, Medical Monitors, Regulatory Affairs, and Data Management. Contribute to risk-based monitoring strategies and support audit readiness. Requirements: 5 years+ experience in clinical project management, preferably in Oncology. Strong knowledge of ICH-GCP and EMA
Freelance - Clinical Project Manager (0.8 FTE) (Remote) employer: EPM Scientific
Join an innovative and rapidly growing biotechnology organisation in West London, where you will play a pivotal role as a Clinical Program Leader. The company fosters a collaborative work culture that encourages professional growth and offers significant career development opportunities, all while providing a competitive salary and flexible hybrid working model. With a strong commitment to scientific excellence and patient-focused research, this is an excellent opportunity for those looking to make a meaningful impact in clinical development.
StudySmarter Expert Advice🤫
We think this is how you could land Freelance - Clinical Project Manager (0.8 FTE) (Remote)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical project management field, especially those with experience in oncology. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and the regulatory environment. We want you to be ready to impress with your expertise and show how you can lead global clinical trials effectively.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview or networking event, drop a quick thank-you email. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Freelance - Clinical Project Manager (0.8 FTE) (Remote)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Clinical Project Manager. Highlight your experience in oncology and any relevant projects you've managed. We want to see how your skills match 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 this freelance role. Share specific examples of your past successes in clinical project management that relate to the job description.
Showcase Your Communication Skills:Since you'll be the main point of contact for stakeholders, it's crucial to demonstrate your communication skills. Use clear and concise language in your application to show us you can convey complex information effectively.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Don’t miss out on this opportunity!
How to prepare for a job interview at EPM Scientific
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology trials and the specific challenges they present. Familiarise yourself with recent advancements in the field, as well as any relevant regulations from EMA and FDA. This will show that you're not just a project manager, but someone who understands the nuances of the industry.
✨Showcase Your Leadership Skills
As a Clinical Project Manager, you'll be leading global teams. Prepare examples of how you've successfully managed teams in the past, especially in remote settings. Highlight your ability to communicate effectively with cross-functional teams and stakeholders, as this is crucial for the role.
✨Be Ready for Compliance Questions
Expect questions about GCP, protocol compliance, and regulatory requirements. Brush up on these topics and be prepared to discuss how you've ensured compliance in previous projects. Providing specific examples will demonstrate your expertise and attention to detail.
✨Prepare for Scenario-Based Questions
Think about potential scenarios you might face in this role, such as managing a crisis at a trial site or dealing with unexpected regulatory changes. Practising your responses to these types of questions can help you articulate your problem-solving skills and adaptability during the interview.
