At a Glance
- Tasks: Lead clinical projects in Oncology, managing timelines, budgets, and team collaboration.
- Company: Precision for Medicine is a people-focused CRO dedicated to advancing oncology research.
- Benefits: Enjoy remote work flexibility, a supportive team environment, and opportunities for professional growth.
- Why this job: Make a real impact on patient health while thriving in a dynamic, collaborative culture.
- Qualifications: 5-7 years in project management within clinical trials, preferably in Oncology.
- Other info: Join a passionate team committed to groundbreaking cancer therapies and work-life balance.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Clinical Project Manager / Senior Clinical Project Manager Remote, United Kingdom Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery? Precision for Medicine (CRO) are looking to hire a (Senior) Project Manager ideally with experience in Oncology who have managed full service clinical trials within a CRO setting to join our global team. In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality. Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout. You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team. We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you. How we will keep you busy and support your growth: You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well. Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations Liaise with Project Team and senior management of both Precision and sponsors, including C level Handle and lead all aspects of a clinical research trial or trials Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc. Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation. Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets Requirements: Degree or similar related life science qualification, or equivalent combination of education and experience. Previous experience in a full service/global Project Management role working in the CRO industry is essential. 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. Experience managing studies within Oncology Working understanding of GCP/ICH guidelines and the clinical development process Ability to drive and availability for domestic and international travel including overnight stays Be able to communicate effectively in the English language both written and spoken Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS) Proven ability to develop positive working relationships with individual and teams internally and externally Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan Precision for Medicine\’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology. We are a people focused CRO with a supportive and collaborative environment which promotes work life balance and encourages team development. We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. Any data provided as a part of this application will be stored in accordance with ourPrivacy Policy. For CA applicants, please also refer to ourCA Privacy Notice . Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com . It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process. 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Clinical Project Manager / Senior Clinical Project Manager Remote, United Kingdom employer: Precisionscientia
Contact Detail:
Precisionscientia Recruiting Team
QuestionForHR@precisionmedicinegrp.com
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager / Senior Clinical Project Manager Remote, United Kingdom
✨Tip Number 1
Network with professionals in the clinical trials and oncology fields. Attend industry conferences, webinars, or local meetups to connect with potential colleagues and learn about job openings that may not be advertised.
✨Tip Number 2
Familiarise yourself with the latest trends and challenges in oncology clinical trials. This knowledge will not only help you in interviews but also demonstrate your passion and commitment to the field.
✨Tip Number 3
Prepare for potential interviews by practising common questions related to project management in clinical trials. Focus on your experience with full-service oversight and how you've successfully managed timelines, budgets, and client relationships.
✨Tip Number 4
Showcase your soft skills during networking and interviews. Emphasise your ability to communicate effectively, build relationships, and work collaboratively within cross-functional teams, as these are crucial for success in this role.
We think you need these skills to ace Clinical Project Manager / Senior Clinical Project Manager Remote, United Kingdom
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical project management, particularly in Oncology. Use specific examples of projects you've managed, focusing on your role and the outcomes achieved.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trials and how your skills align with the job requirements. Mention your consultative approach to trial management and your ability to work with cross-functional teams.
Highlight Relevant Skills: In your application, emphasise your understanding of GCP/ICH guidelines and your proficiency with software tools like CTMS and EDC. These are crucial for the role and will demonstrate your readiness to hit the ground running.
Showcase Your Communication Skills: Since the role involves liaising with clients and stakeholders, provide examples of how you've effectively communicated in previous roles. This could include managing client relationships or presenting project updates.
How to prepare for a job interview at Precisionscientia
✨Show Your Oncology Expertise
Make sure to highlight your experience in managing clinical trials specifically within the Oncology field. Be prepared to discuss specific projects you've worked on, the challenges you faced, and how you overcame them.
✨Demonstrate Your Project Management Skills
Prepare to talk about your project management methodologies and tools. Discuss how you've successfully managed timelines, budgets, and team dynamics in previous roles, especially in a CRO setting.
✨Engage with Stakeholders
Since this role involves liaising with clients and internal teams, be ready to share examples of how you've built positive relationships with stakeholders. Highlight your communication skills and any successful collaborations you've led.
✨Understand GCP/ICH Guidelines
Brush up on Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. Be prepared to discuss how these regulations impact trial management and your approach to ensuring compliance.