At a Glance
- Tasks: Lead clinical trials in Oncology, ensuring project delivery and client satisfaction.
- Company: Precision for Medicine, a supportive and collaborative CRO.
- Benefits: Work-life balance, professional development, and a dynamic team environment.
- Other info: Join a people-focused team that values collaboration and growth.
- Why this job: Make a real impact on patient health while managing innovative clinical projects.
- Qualifications: 5-7 years in project management within clinical trials, especially in Oncology.
The predicted salary is between 55000 - 70000 £ per year.
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 (Senior) 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 (phase 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 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.
Key Responsibilities- You will independently lead clinical projects in accordance with the study budget and scope of work.
- Use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives.
- 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.
- 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 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 individuals 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 is a people-focused CRO with a supportive and collaborative environment which promotes work‐life balance and encourages team development.
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.
Clinical Project Manager in London employer: Precision For Medicine
Precision for Medicine is an exceptional employer that prioritises a supportive and collaborative work environment, fostering a culture of teamwork and innovation. With a strong focus on work-life balance and professional development, employees are encouraged to thrive in their roles while making a meaningful impact on global health through clinical trials in Oncology. Joining our dedicated team means being part of a high-energy atmosphere where your contributions are valued and recognised.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager in London
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We think you need these skills to ace Clinical Project Manager in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Precision For Medicine!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Precision For Medicine that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Precision For Medicine!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Precision For Medicine, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Precision For Medicine
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Precision For Medicine that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Precision For Medicine’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
