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 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.
You love having responsibility and a say in how clinical trials are run
You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.
You are a master at identifying any risks that threaten projects and handle them resolutely
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
Mentoring and training of team members
Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
Bachelor’s degree or equivalent combination of education / experience in science or health-related field, including experience in the field of oncology
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
Availability for domestic and international travel including overnight stays
Must be able to communicate effectively in the English language
Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. 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.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. Precision Medicine Group is an Equal Opportunity Employer. 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
Seniority level Mid-Senior level
Employment type Full-time
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