Clinical Trial Manager
WFA Digital Insight
The demand for clinical trial managers with expertise in oncology has skyrocketed, with a 25% growth in job postings in the last year. Precision for Medicine is at the forefront of precision medicine, and this role offers a unique opportunity to work with a company that's making a real impact in the industry. With the rise of remote work, candidates can now apply from Poland and other European countries. To succeed in this role, candidates will need to have a strong background in clinical trial management, excellent communication skills, and the ability to work autonomously.
Job Description
About the Role
As a Clinical Trial Manager at Precision for Medicine, you will be responsible for the management and operational delivery of clinical elements within a trial. This includes site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities, and close-out. You will be the central point of contact for the study, working closely with other functional team members to ensure the successful execution of the trial.The day-to-day responsibilities of this role will be varied and challenging, requiring a high degree of organizational skills, attention to detail, and ability to work under pressure. You will be working with a team of experienced professionals who are passionate about delivering high-quality results and making a positive impact on patients' lives.
Precision for Medicine is a precision medicine CRO that offers a unique and integrated approach to clinical trial design and delivery. The company is committed to addressing the challenges facing the research and development of novel compounds in oncology and other therapeutic areas.
What You Will Do
- Manage and deliver clinical trials from start-up to close-out, ensuring timely and high-quality execution
- Lead and manage a team of CRAs, providing guidance and support to ensure successful trial delivery
- Develop and implement clinical trial plans, including site selection, enrollment strategies, and monitoring plans
- Collaborate with other functional teams, including data management, biostatistics, and medical writing
- Ensure compliance with GCP/ICH guidelines, regulatory requirements, and company SOPs
- Manage and mitigate risks, developing and implementing contingency plans as needed
- Communicate effectively with stakeholders, including sponsors, investigators, and study teams
- Develop and manage trial budgets, ensuring cost-effective and efficient trial delivery
- Identify and escalate issues, developing and implementing solutions to ensure trial success
What We Are Looking For
- Bachelor's degree or equivalent combination of education and experience in science or health-related field
- Minimum 5 years of experience in clinical trial management, with a focus on oncology
- Proven track record of successful trial delivery, with a strong understanding of clinical trial operations and management
- Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams
- Strong organizational and time management skills, with the ability to prioritize tasks and manage multiple projects
- Experience with GCP/ICH guidelines, regulatory requirements, and company SOPs
- Ability to work autonomously, with a high degree of self-motivation and initiative
- Proficiency in MS Office, MS Project, and other software applications
Nice to Have
- Experience with CTMS, eTMF, EDC, and IXRS systems
- Knowledge of medical terminology and clinical trial activities
- Certification in clinical trial management or a related field
- Experience working in a CRO or pharmaceutical company
Benefits and Perks
- Competitive salary and benefits package
- Opportunity to work with a company that's making a positive impact in the industry
- Collaborative and dynamic work environment
- Professional development and training opportunities
- Flexible working hours and remote work options
- Access to the latest technology and software applications
- Recognition and reward for outstanding performance
How to Stand Out
- Make sure you have a strong understanding of clinical trial operations and management, including GCP/ICH guidelines and regulatory requirements.
- Develop a portfolio that showcases your experience and skills in clinical trial management, including case studies and testimonials.
- Prepare to talk about your experience working with cross-functional teams and your ability to communicate effectively with stakeholders.
- Research the company and the role, and be prepared to ask questions during the interview.
- Highlight your ability to work autonomously and manage multiple projects, and be prepared to provide examples of your experience.
- Don't be afraid to ask about the company culture and values, and how they align with your own goals and motivations.
- Be prepared to discuss your experience with software applications, including CTMS, eTMF, EDC, and IXRS systems.
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