Clinical Study Associate Manager

Cpl
London
10 months ago
Applications closed

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Location: London or Ireland based - 3 days on site.

Contract: 12 months

Rate: Negotiable daily rate

Travel: Travel to study sites may be required to assist with monitoring clinical studies.

Cpl Life Sciences have partnered with a global, well respected Biotechnology company to bring on board a Senior Clinical Research Associate. You will support the Clinical Study Lead and take responsibility for the areas of the clinical trial delivery. You will work with the study team internally and externally with vendors in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Standard Operating Procedures (SOPs). 

Essential requirements:

•BSc degree or higher in a relevant subject

•Experience within Pharmaceutical companies

•Vendor Management Experience

•Experience in Clinical Operations

•Experience in trial management systems, Microsoft applications and TMF

•Good knowledge of Good Clinical Practice and regulatory guidelines

Key Responsibilities are but not limited to:

•Lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study

•Contributes to risk assessment and helps identify risk mitigation strategies

•Supports feasibility assessment to relevant regions and countries

•Oversee and provide input to the development of study specific documentation: case report form (CRF), data management 

•Oversee the engagement, contracting and management of required vendors for the study

•Budget management

•Supports Audit Inspections

•Monitoring recruitment and retention including site activation and monitoring visits

If this roles sounds of interest please apply direct, or send your CV to

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