Clinical Trial Manager

5 hours ago

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pfm medical, inc.

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Medical Device Manufacturing

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Description

• We have an opportunity 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. • 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. • 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. • The day-to-day role includes 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.

Requirements

• 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). • 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. • 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.