Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage clinical trials across multiple countries, ensuring quality and timely delivery.
- Company: Join Precision for Medicine, a leader in precision medicine and oncology research.
- Benefits: Enjoy remote work options and a dynamic, supportive team environment.
- Why this job: Make a real impact on patient health while thriving in a fast-paced, innovative culture.
- Qualifications: Bachelor's degree in a science or health-related field with clinical trial management experience.
- Other info: Opportunity to mentor and lead a passionate team in groundbreaking oncology research.
The predicted salary is between 36000 - 60000 £ per year.
Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.
Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.
You will be the hub of central intelligence for the studies you will be managing and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.
We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don\’t miss exploring working with us.
About You:
- You love having responsibility and a say in how clinical trials are run
- You plan ahead, but have alternative options and a flexible approach
- You are client focused
- You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
- You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly
- You are a master at identifying any risks that threaten projects and handle them resolutely
- You thrive and work with autonomy and ownership to deliver successful outcomes
The day-to-day role, and how we will support your continued growth:
- Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
- Successful execution of assigned trials and ensuring completion of trial deliverables
- Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
- Mentoring and training of team members
- Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
- Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
- Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction
Qualifications:
- Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field ofoncology
Other Required:
- Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated \’clinical lead\’ role).
- Significant clinical trial management experience in the area of oncology
- Working knowledge of GCP/ICH guidelines and the clinical development process
- Availability for domestic and international travel including overnight stays
- Must be able to communicate effectively in the English language
Skills:
- Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
- Demonstrated ability to develop positive working relationships with internal and external organizations
- Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
- Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
#LI-TB1
Any data provided as a part of this application will be stored in accordance with our Privacy 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.
Apply for this job
*
indicates a required field
First Name *
Last Name *
Email *
Phone *
Resume/CV *
Enter manually
Accepted file types: pdf, doc, docx, txt, rtf
Enter manually
Accepted file types: pdf, doc, docx, txt, rtf
Education
School Select…
Degree Select…
Select…
Start date year
LinkedIn Profile
What is your desired salary? *
Are you authorized to work lawfully in the country/location for which you are applying? * Select…
Will you now or in the future require Precision Medicine Group to commence (sponsor) an immigration case in order to employ you (for example, work visa application or work visa transfer, or other-employment based immigration case)? This is sometimes called \”sponsorship\” for an employment-based visa status. * Select…
Have you ever worked for Precision Medicine Group or one of its affiliated companies? * Select…
If yes, when and which company?
Have you ever interviewed with Precision Medicine Group or an affiliated company? * Select…
If yes, when and which company?
Are you currently subject to a Non-Compete or Non-Solicit with your current employer? * Select…
I certify that the information on this application, my resume and any supporting documentation I provide is complete and accurate to the best of my knowledge. If this application leads to employment, I understand that false or misleading information in my application, resume or interview may result in my release or termination of employment. I authorize the Company or its agents to confirm all statements contained in this application and/or curriculum vitae as it relates to the position I am seeking and to the extent permitted by the laws of the country where the job is located (“Applicable Laws”). I agree to complete any required authorization forms for the background investigation. I authorize and consent to, without reservation, any party or agency contracted by this employer to furnish the above-mentioned information. I hereby release, discharge, and hold harmless, to the extent permitted by Applicable Laws, any party delivering information to the Company or its duly authorized representative pursuant to this authorization from any liability, claims, charges or causes of action which I may have as a result of the delivery or disclosure of the above requested information and all other persons, corporations, or organizations furnishing such information. If hired, I understand that I will be required to provide genuine documentation establishing my identity and eligibility to be legally employed in the country where the job is located. I also understand that the Company employs only individuals who are legally eligible to work in the country where the job is located. * Select…
Legal Address – Street Address 1 *
Legal Address – Street Address 2
Legal Address – City *
Legal Address – State * Select…
Legal Address – Zip *
Legal Address – Country * Select…
How many years of experience as a Clinical Lead/ Clinical Trial Manager do you have? *
How many years of oncological therapeutic experience do you have as a Clinical Research Associate ,Clinical Lead and/or Clinical Trial Manager? Please list the oncological trials you had been working on, including the indication and phase of the trial. *
#J-18808-Ljbffr
Clinical Trial Manager employer: Precision For Medicine
Contact Detail:
Precision For Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager
✨Tip Number 1
Familiarise yourself with the latest trends and developments in precision medicine and oncology. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the field, making you a more attractive candidate.
✨Tip Number 2
Network with professionals in the clinical trial management space, especially those who have experience in oncology. Attend relevant webinars or conferences to connect with potential colleagues and learn about their experiences at companies like Precision for Medicine.
✨Tip Number 3
Prepare to discuss specific challenges you've faced in previous clinical trials and how you overcame them. Highlighting your problem-solving skills and adaptability will resonate well with the hiring team, as they value candidates who can thrive in dynamic environments.
✨Tip Number 4
Showcase your leadership abilities by discussing any mentoring or training experiences you've had with team members. This aligns with the role's requirement of leading CRAs and demonstrates your capability to foster a collaborative work environment.
We think you need these skills to ace Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly in oncology. Use specific examples that demonstrate your ability to lead studies across multiple countries and manage timelines effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for precision medicine and your consultative approach to trial management. Mention how your skills align with the company's mission and values, especially regarding rare diseases and oncology.
Highlight Relevant Skills: In your application, emphasise your knowledge of GCP/ICH guidelines and your experience with clinical trial management software. Be specific about your technical skills and how they relate to the role of Clinical Trial Manager.
Showcase Communication Abilities: Since clear communication is crucial for this role, provide examples of how you've successfully managed stakeholder relationships and maintained effective communication in previous projects. This will demonstrate your capability to keep trials running smoothly.
How to prepare for a job interview at Precision For Medicine
✨Showcase Your Experience in Oncology
Make sure to highlight your specific experience in oncology during the interview. Discuss any relevant clinical trials you've managed, focusing on your role and the outcomes achieved. This will demonstrate your expertise and passion for the field.
✨Demonstrate Your Organisational Skills
Given the dynamic nature of clinical trials, it's crucial to showcase your organisational skills. Prepare examples of how you've successfully managed timelines and shifting priorities in past roles, ensuring quality delivery throughout.
✨Communicate Clearly and Concisely
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics like trial management and regulatory compliance. This will help convey your ability to keep teams aligned and informed.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities. Think of potential challenges you might face in managing a clinical trial and prepare creative action plans to address them. This will show your proactive approach and readiness to tackle obstacles.
