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Senior Clinical Research Associate

London – Sarah Cannon Research Institute
Non-clinical
Full time
0022818
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Sarah Cannon Research Institute

Full time, 37.5 hours per week, Monday to Friday

Salary - Competitive

An exciting opportunity has arisen for a Senior Clinical Research Associate (Sr. CRA) to join us as a key member of the team, providing expert advice, guidance and general supervision to the clinical monitoring team on designated projects; ensuring the quality and integrity of data, compliance with regulatory requirements and ensuring that studies are completed on time and within budget.

Duties and Responsibilities

  • Serve as the primary point of contact for investigative sites.

  • Conduct all activities according to the defined project-specific quality and performance standards

  • Serve as a mentor within the organization, working with others to help them organize their time efficiently

  • In-depth knowledge of ICH/GCP and region specific regulations, able to give guidance to junior CRAs on applying this knowledge to the practice of monitoring.

  • Performance of CRA assessment and training visits per SOPs

  • Assist in the development and delivery of departmental trainings

  • Able to give practical guidance on application of systems, processes, and regulations

  • Actively participate in training sessions and workshops, including presenting reports from any conferences attended

  • May be involved in bid defense meetings, kickoff meetings and other sponsor presentations

  • Ensure awareness of project-specific quality and performance standards (within Development Innovations Monitoring Standards) and ensure that these are adequately documented, communicated and understood. Serve as a subject matter expert (SME) within Development Innovations for these standards

Skills and Experience

  • At least five years of CRA experience at a contract research organization (CRO) or sponsor company monitoring clinical trials at investigative sites with direct oncology monitoring experience in Phase l – lll in solid and liquid tumor types

  • Have performed all visit types (PSV, SIV, RMV, and COV)

  • Previous experience in a Sr. CRA role

  • Lead CRA experience

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