Senior CRA

As a Snr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Clinical Research Associate (CRA) you will be dedicated to one of our global Healthcare clients who have a strong legacy of innovation and leading the way within a specialist therapeutic area. They display an ongoing commitment to changing the lives of patients and the accessibility of products in order to change the lives of those that need them.

The CRA is the primary point of contact between site staff and sponsor. This CRA will be responsible for taking leadership of site management for the selection and initiation of sites on behalf of the sponsor, as well as conducting and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, sponsor´s procedures and protocol requirements.

Responsibilities:

• Perform all type of visits from site feasibility to close out visits according to plan, document actions and follow up on action plans
• Train and guide site staff in safety information handling, systems, protocol and trial procedures to minimize protocol deviations
• Proactive use of EDC and other data source systems for preparation and conduct on site visits as well as source data verification in collaboration with data management/logistics team
• Identify potential risks and proactively take action to prevent or mitigate
• Collaborate with Data Management/logistics in resolving queries
• Assist to ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan
• Motivate and build strong relations with site personnel to assist the sponsor in being their preferred clinical research partner
• Collaborate with and provide oversight of deliverables from vendors locally, if applicable
• Support the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF)
• Participate in Investigators Meetings to ensure relations with sites as well as active presentation as applicable
• Maintain knowledge of and act in compliance with global and local SOPs, GCP and other regulatory requirements
• Support audits and inspections at sites and affiliate, as applicable

• Bachelor or Master’s degree in life sciences or other relevant fields.
• At least 2 years of experience as an independent Clinical Research Associate.
• Strong oncology is a must.
• Excellent knowledge of Clinical Trial Management Systems, Good Clinical Practices and Trial Management.
• Strong analytical and communication skills with business, industry understanding and stakeholder management.
• Fluent in both Polish and English.
• Valid driver’s license

You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.