At a Glance
- Tasks: Lead clinical trials in Oncology, managing budgets, timelines, and client relationships.
- Company: Join Precision for Medicine, a people-focused CRO dedicated to innovative cancer therapies.
- Benefits: Enjoy a collaborative environment, work-life balance, and opportunities for professional growth.
- Other info: Remote work options available; must be willing to travel domestically and internationally.
- Why this job: Make a real impact on patient health while thriving in a dynamic, supportive team culture.
- Qualifications: 5-7 years in project management within clinical trials, preferably in Oncology.
The predicted salary is between 36000 - 60000 £ 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 are looking to hire a Clinical Project Manager / Senior Clinical Project Manager 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. You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.
You will be 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 environment. 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 review protocols and other study documentation such as project plans, informed 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.
- Extensive experience working within Clinical Operations position within a CRO, and at least 4 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 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, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.
Clinical Project Manager / Senior Clinical Project Manager employer: Precision Medicine Group
At Precision Medicine Group, we pride ourselves on being an excellent employer by fostering a collaborative and innovative work culture that empowers our employees to make a real impact in the field of clinical research. With fully remote opportunities across the UK, we offer flexible working arrangements, comprehensive benefits, and continuous professional development to support your career growth. Join us to be part of a team that values your contributions and is dedicated to advancing healthcare outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager / Senior Clinical Project Manager
✨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 employers. Building relationships can often lead to job opportunities that aren't advertised.
✨Tip Number 2
Familiarise yourself with the latest trends and challenges in oncology clinical trials. Being knowledgeable about current research, regulatory changes, and innovative trial designs will help you stand out during interviews and discussions with potential employers.
✨Tip Number 3
Prepare for interviews by practising your responses to common project management scenarios in clinical trials. Use the STAR method (Situation, Task, Action, Result) to structure your answers, showcasing your experience and problem-solving skills effectively.
✨Tip Number 4
Demonstrate your leadership and teamwork abilities by sharing specific examples from your past experiences. Highlight how you've successfully managed cross-functional teams and client relationships, as these are crucial skills for a Clinical Project Manager role.
We think you need these skills to ace Clinical Project Manager / Senior Clinical Project Manager
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:Emphasise your understanding of GCP/ICH guidelines and your proficiency with software tools like CTMS and EDC. Include any experience you have with managing budgets and timelines in clinical trials.
Showcase Communication Skills:Since the role involves liaising with clients and stakeholders, demonstrate your strong communication skills in your application. Provide examples of how you've effectively communicated project updates or handled client relationships in the past.
How to prepare for a job interview at Precision Medicine Group
✨Showcase Your Oncology Experience
Make sure to highlight your specific experience in managing clinical trials within the oncology field. Discuss any relevant projects you've led, focusing on the challenges you faced and how you overcame them.
✨Demonstrate Your Project Management Skills
Be prepared to discuss your project management methodologies and tools. Share examples of how you've successfully managed timelines, budgets, and team dynamics in previous roles, especially in a CRO setting.
✨Prepare for Client Interaction Scenarios
Since this role involves liaising with clients, think of scenarios where you've had to manage client expectations or resolve conflicts. Be ready to explain how you maintain strong relationships and ensure excellent customer service.
✨Understand GCP/ICH Guidelines
Brush up on Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. Be ready to discuss how these regulations impact trial management and your approach to ensuring compliance throughout the project lifecycle.
